Womens health continued Flashcards

1
Q

what is cervical cancer strongly associated with

A

HPV - 16 and 18

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2
Q

how does HPV predispose someone to cancer

A

P53 and pRb are tumour suppressor genes. They have a role in suppressing cancers from developing. HPV produces two proteins (E6 and E7) that inhibit these tumour suppressor genes. The E6 protein inhibits p53, and the E7 protein inhibits pRb. Therefore, HPV promotes the development of cancer by inhibiting tumour suppressor genes.

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3
Q

what are risk factors for cervical cancer

A

Increased risk of catching HPV
Later detection of precancerous and cancerous changes (non-engagement with screening)
Smoking
HIV (patients with HIV are offered yearly smear tests)
Combined contraceptive pill use for more than five years
Increased number of full-term pregnancies
Family history
Exposure to diethylstilbestrol during fetal development (this was previously used to prevent miscarriages before 1971)

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4
Q

what are increased risks of catching HPV

A

Early sexual activity
Increased number of sexual partners
Sexual partners who have had more partners
Not using condoms

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5
Q

how does cervical cancer present

A

may be detected during cervical smears in otherwise asymptomatic women
abnormal vaginal bleeding
vaginal discharge
pelvic pain
dyspareunia

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6
Q

what are appearances which may suggest cervical cancer

A

Ulceration
Inflammation
Bleeding
Visible tumour

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7
Q

what are the grades of cervical intraepithelial neoplasia

A

CIN I: mild dysplasia, affecting 1/3 the thickness of the epithelial layer, likely to return to normal without treatment
CIN II: moderate dysplasia, affecting 2/3 the thickness of the epithelial layer, likely to progress to cancer if untreated
CIN III: severe dysplasia, very likely to progress to cancer if untreated

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8
Q

what are notable exceptions for the smear test

A

Women with HIV are screened annually
Women over 65 may request a smear if they have not had one since aged 50
Women with previous CIN may require additional tests (e.g. test of cure after treatment)
Certain groups of immunocompromised women may have additional screening (e.g. women on dialysis, cytotoxic drugs or undergoing an organ transplant)
Pregnant women due a routine smear should wait until 12 weeks post-partum

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9
Q

when are women called to the cervical screening programme

A

Every three years aged 25 – 49
Every five years aged 50 – 64

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10
Q

what are the different cytology results someone can get

A

Inadequate
Normal
Borderline changes
Low-grade dyskaryosis
High-grade dyskaryosis (moderate)
High-grade dyskaryosis (severe)
Possible invasive squamous cell carcinoma
Possible glandular neoplasia

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11
Q

what is the management for different smear results based on the public health england guidelines

A

Inadequate sample – repeat the smear after at least three months
HPV negative – continue routine screening
HPV positive with normal cytology – repeat the HPV test after 12 months
HPV positive with abnormal cytology – refer for colposcopy

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12
Q

what is colposcopy

A

it is when a speculum is inserted and uses a colposcope to magnify the cervix which allows the epithelial lining of the cervix to be examined
stains such as acetic acid and iodine solution can be used to differentiate abnormal areas

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13
Q

what is acetic acid

A

causes abnormal cells to appear white. This appearance is described as acetowhite. This occurs in cells with an increased nuclear to cytoplasmic ratio (more nuclear material), such as cervical intraepithelial neoplasia and cervical cancer cells.

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14
Q

what is schillers iodine test

A

involves using an iodine solution to stain the cells of the cervix. Iodine will stain healthy cells a brown colour. Abnormal areas will not stain.

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15
Q

what is large loop excision of the transformation zone

A

it is a procedure called a loop biopsy which can be performed with local anaesthetic during colposcopy, which involves using diathermy to remove abnormal epithelial tissue of the cervix

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16
Q

what is a cone biopsy

A

it is a treatment for cervical intraepithelial neoplasia and very early stages of cervical cancer. The surgeons removes a cone shaped piece of cervix

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17
Q

what are the main risks of a cone biopsy

A

Pain
Bleeding
Infection
Scar formation with stenosis of the cervix
Increased risk of miscarriage and premature labour

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18
Q

what is the staging used for cervical cancer

A

The International Federation of Gynaecology and Obstetrics (FIGO) staging system is used to stage cervical cancer:

Stage 1: Confined to the cervix
Stage 2: Invades the uterus or upper 2/3 of the vagina
Stage 3: Invades the pelvic wall or lower 1/3 of the vagina
Stage 4: Invades the bladder, rectum or beyond the pelvis

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19
Q

what is the management of cervical cancer

A

Cervical intraepithelial neoplasia and early-stage 1A: LLETZ or cone biopsy
Stage 1B – 2A: Radical hysterectomy and removal of local lymph nodes with chemotherapy and radiotherapy
Stage 2B – 4A: Chemotherapy and radiotherapy
Stage 4B: Management may involve a combination of surgery, radiotherapy, chemotherapy and palliative care

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20
Q

what is the five year survival for cervical cancer

A

The 5-year survival drops significantly with more advanced cervical cancer, from around 98% with stage 1A to around 15% with stage 4

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21
Q

what is pelvic exenteration

A

an operation that may be used in advanced cervical cancer. It involves removing most or all of the pelvic organs, including the vagina, cervix, uterus, fallopian tubes, ovaries, bladder and rectum. It is a vast operation and has significant implications on quality of life.

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22
Q

what is Bevacizumab

A

monoclonal antibody that may be used in combination with other chemotherapies in the treatment of metastatic or recurrent cervical cancer. It is also used in several other types of cancer. It targets vascular endothelial growth factor A (VEGF-A), which is responsible for the development of new blood vessels.

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23
Q

when is the HPV vaccine given and what does it protect you against

A

12-13 yrs before sexual activity
The current NHS vaccine is Gardasil, which protects against strains 6, 11, 16 and 18:

Strains 6 and 11 cause genital warts
Strains 16 and 18 cause cervical cancer

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24
Q

what is the most common type of endometrial cancer

A

adenocarcinoma
it is an oestrogen sensitive cancer

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25
Q

what is endometrial hyperplasia

A

precancerous condition involving thickening of the endometrium. The risk factors, presentation and investigations of endometrial hyperplasia are similar to endometrial cancer. Most cases of endometrial hyperplasia will return to normal over time

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26
Q

what are the two kinds of endometrial hyperplasia

A

hyperplasia without atypia
atypical hyperplasia

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27
Q

how is endometrial hyperplasia treated

A

progestogens, with either:
Intrauterine system (e.g. Mirena coil)
Continuous oral progestogens (e.g. medroxyprogesterone or levonorgestrel)

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28
Q

what are risk factors for endometrial cancer

A

unopposed oestrogen
Increased age
Earlier onset of menstruation
Late menopause
Oestrogen only hormone replacement therapy
No or fewer pregnancies
Obesity
Polycystic ovarian syndrome
Tamoxifen
type 2 diabetes
hereditary nonpolyposis colorecta cancer/lynch syndrome

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29
Q

for endometrial protection what should women with PCOS be given

A

one of:
The combined contraceptive pill
An intrauterine system (e.g. Mirena coil)
Cyclical progestogens to induce a withdrawal bleed.

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30
Q

what are protective factors against endometrial cancer

A

Combined contraceptive pill
Mirena coil
Increased pregnancies
Cigarette smoking

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31
Q

how does smoking affect the risk of endometrial cancer

A

it reduces the risk of it as it is anti-oestrogenic
Oestrogen may be metabolised differently in smokers
Smokers tend to be leaner, meaning they have less adipose tissue and aromatase enzyme
Smoking destroys oocytes (eggs), resulting in an earlier menopause

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32
Q

how does endometrial cancer present

A

postmenopausal bleeding
Postcoital bleeding
Intermenstrual bleeding
Unusually heavy menstrual bleeding
Abnormal vaginal discharge
Haematuria
Anaemia
Raised platelet count

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33
Q

what is the referral criteria for endometrial cancer

A

The referral criteria for a 2-week-wait urgent cancer referral for endometrial cancer is:
Postmenopausal bleeding (more than 12 months after the last menstrual period)
NICE also recommends referral for a transvaginal ultrasound in women over 55 years with:
Unexplained vaginal discharge
Visible haematuria plus raised platelets, anaemia or elevated glucose levels

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34
Q

what investigations are done for suspected endometrial cancer

A

Transvaginal ultrasound for endometrial thickness (normal is less than 4mm post-menopause)
Pipelle biopsy, which is highly sensitive for endometrial cancer making it useful for excluding cancer
Hysteroscopy with endometrial biopsy

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35
Q

what are the stages of endometrial cancer

A

The International Federation of Gynaecology and Obstetrics (FIGO) staging system is used to stage endometrial cancer:

Stage 1: Confined to the uterus
Stage 2: Invades the cervix
Stage 3: Invades the ovaries, fallopian tubes, vagina or lymph nodes
Stage 4: Invades bladder, rectum or beyond the pelvis

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36
Q

how is endometrial cancer treated

A

The usual treatment for stage 1 and 2 endometrial cancer is a total abdominal hysterectomy with bilateral salpingo-oophorectomy, also known as a TAH and BSO
other treatment options include:
A radical hysterectomy involves also removing the pelvic lymph nodes, surrounding tissues and top of the vagina
Radiotherapy
Chemotherapy
Progesterone may be used as a hormonal treatment to slow the progression of the cancer

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37
Q

what are the types of ovarian cancers

A

Epithelial cell tumours
dermoid cysts/germ cell tumours
sex cord stromal tumours
metastasis

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38
Q

what is an epithelial cell ovarian tumour

A

Epithelial cell tumours (tumours arising from the epithelial cells of the ovary) are the most common type. Subtypes of epithelial cell tumours include:
Serous tumours (the most common)
Endometrioid carcinomas
Clear cell tumours
Mucinous tumours
Undifferentiated tumours

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39
Q

what are dermoid cysts/germ cell ovarian tumours

A

These are benign ovarian tumours. They are teratomas, meaning they come from the germ cells. They may contain various tissue types, such as skin, teeth, hair and bone. They are particularly associated with ovarian torsion. Germ cell tumours may cause raised alpha-fetoprotein (α-FP) and human chorionic gonadotrophin (hCG).

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40
Q

what are sex cord stromal ovarian tumours

A

These are rare tumours, that can be benign or malignant. They arise from the stroma (connective tissue) or sex cords (embryonic structures associated with the follicles). There are several types, including Sertoli–Leydig cell tumours and granulosa cell tumours.

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41
Q

what is a Krukenberg tumour

A

a metastasis in the ovary, usually from a gastrointestinal tract cancer, particularly the stomach. Krukenberg tumours have characteristic “signet-ring” cells on histology, which look like signet rings on under a microscopy.

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42
Q

what are risk factors for ovarian cancer

A

Age (peaks age 60)
BRCA1 and BRCA2 genes (consider the family history)
Increased number of ovulations
Obesity
Smoking
Recurrent use of clomifene
early onset periods
late menopause
no pregnancies

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43
Q

what are protective factors for ovarian cancer

A

Having a higher number of lifetime ovulations increases the risk of ovarian cancer. Factors that stop ovulation or reduce the number of lifetime ovulations, reduce the risk:

Combined contraceptive pill
Breastfeeding
Pregnancy

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44
Q

how do ovarian tumours present

A

non specific symptoms:
Abdominal bloating
Early satiety (feeling full after eating)
Loss of appetite
Pelvic pain
Urinary symptoms (frequency / urgency)
Weight loss
Abdominal or pelvic mass
Ascites
ovarian mass may press on the obturator nerve and cause referred hip/groin pain

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45
Q

what is the referral criteria for ovarian cancer

A

Refer directly on a 2-week-wait referral if a physical examination reveals:
Ascites
Pelvic mass (unless clearly due to fibroids)
Abdominal mass

carry out further investigations before referral in women presenting with symptoms of possible cancer with a CA125: new Sx of IBS, abdo bloating, early satiety, pelvic pain, urinary frequency and weight loss

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46
Q

what investigations are done for ovarian cancer

A

primary care: CA125 blood test (>35IU/ml is sig) and pelvic ultrasound
look at the risk of malignancy index which takes into account: menopausal status, ultrasound findings and CA125 levels
imaging: CT, histology, pancreatitis

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47
Q

what do women under 40 with a complex ovarian mass require investigation wise

A

require tumour markers for a possible germ cell tumour
- alpha fetoprotein
- human chorionic gonadotropin

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48
Q

what are causes pf raised CA125

A

CA125 is a tumour marker for epithelial cell ovarian cancer. It is not very specific, and there are many non-malignant causes of a raised CA125:
Endometriosis
Fibroids
Adenomyosis
Pelvic infection
Liver disease
Pregnancy

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49
Q

what are the stages of ovarian cancer

A

The International Federation of Gynaecology and Obstetrics (FIGO) staging system is used to stage ovarian cancer. A very simplified version of this staging system is:

Stage 1: Confined to the ovary
Stage 2: Spread past the ovary but inside the pelvis
Stage 3: Spread past the pelvis but inside the abdomen
Stage 4: Spread outside the abdomen (distant metastasis)

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50
Q

what is the management of ovarian cancer

A

Ovarian cancer will be managed by a specialist gynaecology oncology MDT. It usually involves a combination of surgery and chemotherapy.

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51
Q

what is the most common type of vulval cancer

A

squamous cell carcinomas

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52
Q

what are risk factors for vulval cancer

A

Advanced age (particularly over 75 years)
Immunosuppression
Human papillomavirus (HPV) infection
Lichen sclerosus
Around 5% of women with lichen sclerosus get vulval cancer.

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53
Q

what is vulval intraepithelial neoplasia

A

it is a premalignant condition which affects the squamous epithelium of the skin that can precede vulval cancer

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54
Q

what is High grade squamous intraepithelial lesion

A

it is a type of VIN associated with HPV infection that typically occurs in younger women aged 35 – 50 years.

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55
Q

what is Differentiated VIN

A

alternative type of VIN associated with lichen sclerosus and typically occurs in older women (aged 50 – 60 years).

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56
Q

what are the treatment options for VIN

A

Watch and wait with close followup
Wide local excision (surgery) to remove the lesion
Imiquimod cream
Laser ablation

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57
Q

how does vulval cancer present

A

Vulval lump
Ulceration
Bleeding
Pain
Itching
Lymphadenopathy in the groin
Vulval cancer most frequently affects the labia majora, giving an appearance of:
Irregular mass
Fungating lesion
Ulceration
Bleeding

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58
Q

what is the referral criteria for vulval cancer

A

Suspected vulval cancer should be referred on a 2-week-wait urgent cancer referral.
Establishing the diagnosis and staging involves:
Biopsy of the lesion
Sentinel node biopsy to demonstrate lymph node spread
Further imaging for staging (e.g. CT abdomen and pelvis)

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59
Q

what system is used to stage vulval cancer

A

The International Federation of Gynaecology and Obstetrics (FIGO) system is used to stage vulval cancer.

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60
Q

what is the management of vulval cancer

A

Wide local excision to remove the cancer
Groin lymph node dissection
Chemotherapy
Radiotherapy

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61
Q

when should infertility be investigated

A

when a couple has been trying to conceive for 12 months without success

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62
Q

what are causes of fertility issues

A

Sperm problems (30%)
Ovulation problems (25%)
Tubal problems (15%)
Uterine problems (10%)
Unexplained (20%)
40% of infertile couples have a mix of male and female causes.

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63
Q

what is general advice given to people to improve fertility issues

A

The woman should be taking 400mcg folic acid daily
Aim for a healthy BMI
Avoid smoking and drinking excessive alcohol
Reduce stress as this may negatively affect libido and the relationship
Aim for intercourse every 2 – 3 days
Avoid timing intercourse

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64
Q

what investigations are done with fertility issues

A

in primary care: BMI, chlamydia screen, semen analysis, female hormone testing, rubella immunity in mother
in secondary care: ultrasound of pelvis, hysterosalpingogram, laparoscopy and dye test

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65
Q

what female hormones are tested when investigating fertility issues

A

Serum LH and FSH on day 2 to 5 of the cycle
Serum progesterone on day 21 of the cycle (or 7 days before the end of the cycle if not a 28-day cycle).
Anti-Mullerian hormone
Thyroid function tests when symptoms are suggestive
Prolactin (hyperprolactinaemia is a cause of anovulation) when symptoms of galactorrhea or amenorrhoea

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66
Q

why is anti-mullerian hormone tested

A

Anti-Mullerian hormone can be measured at any time during the cycle and is the most accurate marker of ovarian reserve. It is released by the granulosa cells in the follicles and falls as the eggs are depleted. A high level indicates a good ovarian reserve.

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67
Q

what is a hysterosalpingogram

A

type of scan used to assess the shape of the uterus and the patency of the fallopian tubes, via a small tube which is inserted into the cervix and a contrast medium is injected into the uterine cavity and fallopian tubes. If the dye doesnt fill the tubes then this will be seen on X ray and suggests obstruction
tubal cannulation under Xray guidance can be performed during the procedure to open the tubed

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68
Q

what is laparoscopy and dye test

A

During the procedure, dye is injected into the uterus and should be seen entering the fallopian tubes and spilling out at the ends of the tubes. This will not be seen when there is tubal obstruction. During laparoscopy, the surgeon can also assess for endometriosis or pelvic adhesions and treat these.

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69
Q

what is the management options for anovulation

A

weight loss for overweight patients
clomifene
letrozole - used instead of clomifene to stimulate ovulation
gonadotropins - stimulate ovulation in women resistant to clomifene
ovarian drilling
metformin

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70
Q

what is clomifene

A

anti-oestrogen (a selective oestrogen receptor modulator). It is given on days 2 to 6 of the menstrual cycle. It stops the negative feedback of oestrogen on the hypothalamus, resulting in a greater release of GnRH and subsequently FSH and LH.
it is used to help stimulate ovulation

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71
Q

what is the management for tubal factors causing fertility issues

A

Tubal cannulation during a hysterosalpingogram
Laparoscopy to remove adhesions or endometriosis
In vitro fertilisation (IVF)

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72
Q

what is the management for sperm problems causing infertility

A

surgical sperm retrieval
surgical correction of obstruction is present
intra-uterine insemination
intracytoplasmic sperm injection - injecting sperm directly into cytoplasm of egg
donor insemination

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73
Q

what are instructions given to men providing a sample for semen analysis

A

Abstain from ejaculation for at least 3 days and at most 7 days
Avoid hot baths, sauna and tight underwear during the lead up to providing a sample
Attempt to catch the full sample
Deliver the sample to the lab within 1 hour of ejaculation
Keep the sample warm (e.g. in underwear) before delivery

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74
Q

what factors can affect semen analysis and sperm quality and quantity

A

Several lifestyle factors may affect the results of semen analysis and the quality and quantity of sperm:
Hot baths
Tight underwear
Smoking
Alcohol
Raised BMI
Caffeine

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75
Q

what are the normal results indicated by the WHO for semen analysis

A

Semen volume (more than 1.5ml)
Semen pH (greater than 7.2)
Concentration of sperm (more than 15 million per ml)
Total number of sperm (more than 39 million per sample)
Motility of sperm (more than 40% of sperm are mobile)
Vitality of sperm (more than 58% of sperm are active)
Percentage of normal sperm (more than 4%)

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76
Q

what is polyspermia

A

it is a high number of sperm in a sample - more than 250 million per ml

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77
Q

what is oligospermia

A

it is a reduced number of sperm in the semen sample:
Mild oligospermia (10 to 15 million / ml)
Moderate oligospermia (5 to 10 million / ml)
Severe oligospermia (less than 5 million / ml)

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78
Q

what is cryptozoospermia

A

refers to very few sperm in the semen sample (less than 1 million / ml).

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79
Q

what are pre-testicular causes of abnormal semen analysis

A

Testosterone is necessary for sperm creation. The hypothalamo-pituitary-gonadal axis controls testosterone. Hypogonadotrophic hypogonadism (low LH and FSH resulting in low testosterone), can be due to:
Pathology of the pituitary gland or hypothalamus
Suppression due to stress, chronic conditions or hyperprolactinaemia
Kallman syndrome

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80
Q

what are testicular causes of abnormal semen analysis

A

Testicular damage from:
Mumps
Undescended testes
Trauma
Radiotherapy
Chemotherapy
Cancer

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81
Q

what genetic/congenital disorders can affect sperm

A

Klinefelter syndrome
Y chromosome deletions
Sertoli cell-only syndrome
Anorchia (absent testes)

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82
Q

what are post testicular causes of abnormal semen analysis

A

Obstruction preventing sperm being ejaculated can be caused by:

Damage to the testicle or vas deferens from trauma, surgery or cancer
Ejaculatory duct obstruction
Retrograde ejaculation
Scarring from epididymitis, for example, caused by chlamydia
Absence of the vas deferens (may be associated with cystic fibrosis)
Young’s syndrome (obstructive azoospermia, bronchiectasis and rhinosinusitis)

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83
Q

what investigations should be done if someone has an abnormal semen analysis

A

The initial steps for investigating abnormal semen analysis include a history, examination, repeat sample and ultrasound of the testes.
Hormonal analysis with LH, FSH and testosterone levels
Genetic testing
Further imaging, such as transrectal ultrasound or MRI
Vasography, which involves injecting contrast into the vas deferens and performing xray to assess for obstruction
Testicular biopsy

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84
Q

what is the management for abnormal sperm sample

A

Management depends on the underlying cause, and can involve:

Surgical sperm retrieval where there is obstruction
Surgical correction of an obstruction in the vas deferens
Intra-uterine insemination involves separating high-quality sperm, then injecting them into the uterus
Intracytoplasmic sperm injection (ICSI) involves injecting sperm directly into the cytoplasm of an egg
Donor insemination involves sperm from a donor

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85
Q

what is in vitro fertilisation

A

fertilising an egg with sperm in a lab, then injecting the resulting embryo into the uterus

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86
Q

what is the percentage success rate for IVF

A

Each attempt has a roughly 25 – 30% success rate at producing a live birth.

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87
Q

what are the steps in the process of IVF

A

Suppressing the natural menstrual cycle
Ovarian stimulation
Oocyte collection
Insemination / intracytoplasmic sperm injection (ICSI)
Embryo culture
Embryo transfer

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88
Q

what are the protocols for suppressing the menstrual cycle in IVF

A

two protocols
1. GnRH agonists - goserelin injected in the luteal phase which stimulates the pituitary gland to secrete high FSH/LH. This causes negative feedback and the natural production of GnRH is suppressed
2. GnRH antagonist protocol: daily subcutaneous infections of GnRH antagonist starting from day 5-6 of ovarian stimulation. This suppresses LH

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89
Q

what is ovarian stimulation

A

it involves using medications to promote the development of multiple follicles in the ovaries
- done with subcutaneous injections of FSH over 10-14 days
- when enough follicle have developed to an adequate size, FSH is stopped and hCG is given to stimulate the final maturation of the follicles

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90
Q

how are oocytes collected in IVF

A

a needle is inserted through the vaginal wall into each ovary to aspirate the fluid from each follicle which will contain the mature oocytes
- done under guidance of transvaginal ultrasound scan and under sedation (Not GA)

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91
Q

how does oocyte insemination occur in IVF

A

The male produces a semen sample around the time of oocyte collection. Frozen sperm from earlier samples may be used. The sperm and egg are mixed in a culture medium. Thousands of sperm need to be combined with each oocyte to produce enough enzymes (e.g. hyaluronic acid) for one sperm to penetrate the corona radiata and zona pellucida and fertilise the egg.

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92
Q

how long is the embryo cultured for in IVF

A

Dishes containing the fertilised eggs are left in an incubator and observed over 2 – 5 days to see which will develop and grow. They are monitored until they reach the blastocyst stage of development (around day 5).

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93
Q

when are embryos transferred into the mother in IVF

A

After 2 – 5 days, the highest quality embryos are selected for transfer. A catheter is inserted under ultrasound guidance through the cervix into the uterus. A single embryo is injected through the catheter into the uterus, and the catheter is removed. Generally, only a single embryo is transferred. Two embryos may be transferred in older women (i.e. over 35 years). Any remaining embryos can be frozen for future attempts at transfer.

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94
Q

when is a pregnancy test performed in IVF

A

around day 16

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95
Q

what is given to the woman from the time of oocyte collection until 8-10 weeks gestation in IVF

A

progesterone - used to mimic the progesterone released by the corpus luteum during a typical pregnancy

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96
Q

what are the complications of IVF

A

Failure
Multiple pregnancy
Ectopic pregnancy
Ovarian hyperstimulation syndrome
There is a small risk of complications relating to the egg collection procedure:
Pain
Bleeding
Pelvic infection
Damage to the bladder or bowel

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96
Q

what is ovarian hyperstimulation syndrome

A

it is a complication of ovarian stimulation during IVF infertility treatment and is associated with the use of hCG to mature the follicles during the final steps of ovarian stimulation

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97
Q

what is the pathophysiology of OHSS

A

an increase in VEGF released by the granulosa cells of the follicles. This increased vascular permeability causing fluid to lead from the capillaries which can move into the extravascular space and cause oedema, ascites and hypovolaemia
use of LH/FSH during ovarian stimulation results in the development of multiple follicles. OHSS is provoked by the trigger injection of hCG which stimulates the release of VEGF from follicles and cause the condition

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98
Q

what are risk factors for OHSS

A

Younger age
Lower BMI
Raised anti-Müllerian hormone
Higher antral follicle count
Polycystic ovarian syndrome
Raised oestrogen levels during ovarian stimulation

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99
Q

how can OHSS be prevented

A

Women are individually assessed for their risk of developing OHSS.

During stimulation with gonadotrophins, they are monitored with:
Serum oestrogen levels (higher levels indicate a higher risk)
Ultrasound monitor of the follicles (higher number and larger size indicate a higher risk)

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100
Q

what strategies are put in place with women who are at high risk of OHSS

A

Use of the GnRH antagonist protocol (rather than the GnRH agonist protocol)
Lower doses of gonadotrophins
Lower dose of the hCG injection
Alternatives to the hCG injection (i.e. a GnRH agonist or LH)

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101
Q

what are features of OHSS

A

Early OHSS presents within 7 days of the hCG injection. Late OHSS presents from 10 days onwards. Features of the condition include:
Abdominal pain and bloating
Nausea and vomiting
Diarrhoea
Hypotension
Hypovolaemia
Ascites
Pleural effusions
Renal failure
Peritonitis from rupturing follicles releasing blood
Prothrombotic state (risk of DVT and PE)

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102
Q

what are the different severities of OHSS

A

Mild: Abdominal pain and bloating
Moderate: Nausea and vomiting with ascites seen on ultrasound
Severe: Ascites, low urine output (oliguria), low serum albumin, high potassium and raised haematocrit (>45%)
Critical: Tense ascites, no urine output (anuria), thromboembolism and acute respiratory distress syndrome (ARDS)

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103
Q

what is the management of OHSS

A

Oral fluids
Monitoring of urine output
Low molecular weight heparin (to prevent thromboembolism)
Ascitic fluid removal (paracentesis) if required
IV colloids (e.g. human albumin solution)
- patients with mild to moderate are usually managed as an outpatient. Severe cases require admission and critical cases may require admission to ICU

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104
Q

what might be monitored to assess the volume of fluid in the intravascular space in OHSS

A

Haematocrit - when this goes up, this indicates less fluid in the intravascular space as the blood is becoming more concentrated

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105
Q

what is recurrent pregnancy loss

A

it is three or more consecutive miscarriages

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106
Q

what is the risk of miscarriage in different age groups

A

10% in women aged 20 – 30 years
15% in women aged 30 – 35 years
25% in women aged 35 – 40 years
50% in women aged 40 – 45 years

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107
Q

when are investigations initiated for recurrent miscarriage

A

Three or more first-trimester miscarriages
One or more second-trimester miscarriages

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108
Q

what are causes of recurrent miscarriage

A

Idiopathic (particularly in older women)
Antiphospholipid syndrome
Hereditary thrombophilias
Uterine abnormalities
Genetic factors in parents (e.g. balanced translocations in parental chromosomes)
Chronic histiocytic intervillositis
Other chronic diseases such as diabetes, untreated thyroid disease and systemic lupus erythematosus (SLE)

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109
Q

what is antiphospholipid syndrome

A

disorder associated with antiphospholipid antibodies, where blood becomes prone to clotting. The patient is in a hyper-coagulable state. The main associations are with thrombosis and complications in pregnancy, particularly recurrent miscarriage.

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110
Q

how is the risk of miscarriage reduced in women with antiphospholipid syndrome

A

Low dose aspirin
Low molecular weight heparin (LMWH)

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111
Q

what are the key inherited thrombophilia’s to remember

A

Factor V Leiden (most common)
Factor II (prothrombin) gene mutation
Protein S deficiency

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112
Q

what uterine abnormalities can cause recurrent miscarriages

A

Uterine septum (a partition through the uterus)
Unicornuate uterus (single-horned uterus)
Bicornuate uterus (heart-shaped uterus)
Didelphic uterus (double uterus)
Cervical insufficiency
Fibroids

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113
Q

what is chronic histiocytic intervillositis

A

rare cause of recurrent miscarriage, particularly in the second trimester
histocytes and macrophages build up in the placenta causing inflammation and adverse outcomes

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114
Q

how is chronic histiocytic intervillositis diagnosed

A

placental histology showing infiltrates of mononuclear cells in the intervillous spaces

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115
Q

what investigations can be done in someone having recurrent miscarriages

A

Antiphospholipid antibodies
Testing for hereditary thrombophilias
Pelvic ultrasound
Genetic testing of the products of conception from the third or future miscarriages
Genetic testing on parents

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116
Q

what is the management of recurrent miscarriage

A

depends on underlying cause
PRISM trial that suggests a benefit to using vaginal progesterone pessaries during early pregnancy for women with recurrent miscarriages presenting with bleeding

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117
Q

what is the legal requirements for an abortion

A

The legal framework for a termination of pregnancy is the 1967 Abortion Act. The 1990 Human Fertilisation and Embryology Act altered and expanded the criteria for an abortion, and reduced the latest gestational age where an abortion is legal from 28 weeks to 24 weeks.
- two registered medical practitioners must sign to agree an abortion is indicated
- must be carried out in NHS hospital or approved premise

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118
Q

what are the criteria for performing an abortion on someone

A

An abortion can be performed before 24 weeks if continuing the pregnancy involves greater risk to the physical or mental health of:
- The woman
- Existing children of the family
The threshold for when the risk of continuing the pregnancy outweighs the risk of terminating the pregnancy is a matter of clinical judgement and opinion of the medical practitioners.

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119
Q

when can an abortion be performed at any time of a pregnancy

A

Continuing the pregnancy is likely to risk the life of the woman
Terminating the pregnancy will prevent “grave permanent injury” to the physical or mental health of the woman
There is “substantial risk” that the child would suffer physical or mental abnormalities making it seriously handicapped

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120
Q

what pre-abortion care is given

A
  • abortion services can be accessed by self referral, by GP, GUM or family planning
  • Marie stopes UK is a remote service for women less than 10 weeks pregnant
  • women should be offered counselling and information to help decision making from a trained practitioner
  • informed consent is essential
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121
Q

what is given for a medical abortion

A

Mifepristone (anti-progestogen) - halts the pregnancy and relaxing the cervix
misoprostol (prostaglandin analogue) 1-2 days later - softens cervix and stimulates uterine contractions
rhesus negative women with a gestational age of 10 weeks or above having a medical TOP should have anti-D prophylaxis

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122
Q

what is done for a surgical abortion

A

cervical dilation and suction of the contents of the uterus (usually up to 14 weeks)
cervical dilation and evacuation using forceps (between 14 and 24 weeks)
- prior to surgical abortion medications are used for cervical priming which involves softening and dilating of the cervix: misoprostol, mifepristone or osmotic dilators
- rhesus negative women having surgical TOP should have anti-D prophylaxis

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123
Q

what is done for post abortion care

A

women may experience vaginal bleeding and cramps for up to 2 weeks after the procedure
a urine pregnancy test is performed 3 weeks after the abortion to confirm it is complete
contraception is discussed and started where appropriate

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124
Q

what are complications of abortion

A

Bleeding
Pain
Infection
Failure of the abortion (pregnancy continues)
Damage to the cervix, uterus or other structures

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125
Q

when does nausea and vomiting peak in pregnancy

A

8-12 weeks

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126
Q

what is severe nausea and vomiting in pregnancy

A

hyperemesis gravidarum

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127
Q

what hormone is thought to be responsible for nausea and vomiting in pregnancy

A

hCG

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128
Q

what is the diagnosis criteria for hyperemesis gravidarum

A

RCOG guideline (2016) diagnoses hyperemesis are protracted nausea and vomiting in pregnancy plus:
More than 5 % weight loss compared with before pregnancy
Dehydration
Electrolyte imbalance

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129
Q

how is the severity of hyperemesis gravidarum assessed

A

The severity can be assessed using the Pregnancy-Unique Quantification of Emesis (PUQE) score. This gives a score out of 15:
< 7: Mild
7 – 12: Moderate
> 12: Severe

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130
Q

what is the management of hyperemesis gravidarum

A

Antiemetics:
1. prochlorperazine (stemetil)
2. cyclizine
3. ondansetron
4. metoclopramide
ranitidine and omeprazole can be used if acid reflux is a problem
mild cases can be managed with oral antiemetics, moderate-severe cases may require ambulatory care or admission

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131
Q

when might someone need admission for hyperemesis gravidarum

A

Unable to tolerate oral antiemetics or keep down any fluids
More than 5 % weight loss compared with pre-pregnancy
Ketones are present in the urine on a urine dipstick (2 + ketones on the urine dipstick is significant)
Other medical conditions need treating that required admission

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132
Q

what might be done in hospital for hyperemesis gravidarum

A

IV or IM antiemetics
IV fluids (normal saline with added potassium chloride)
Daily monitoring of U&Es while having IV therapy
Thiamine supplementation to prevent deficiency (prevents Wernicke-Korsakoff syndrome)
Thromboprophylaxis (TED stocking and low molecular weight heparin) during admission

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133
Q

what dose of folic acid should women with epilepsy be taking if pregnant

A

5mg daily

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134
Q

how is rheumatoid arthritis managed in pregnancy

A
  • needs to be well controlled for at least three months before becoming pregnant
  • often the symptoms of RA will improve with - pregnancy and flare after delivery
  • treatment regime will need to be altered by a specialist: methotrexate is contraindicated, hydroxychloroquine is safe and considered first line. sulfasalazine is safe and corticosteroids may be used during flare ups
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135
Q

what is recommended for use of NSAIDs in pregnancy

A

tend to be avoided due to them blocking prostaglandins (important in maintaining the ductus arteriosus as well as softening cervix and stimulating contractions) unless they are really necessary
- particularly avoided in third trimester

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136
Q

are beta blockers used in pregnancy

A

they are used most frequently in pregnancy for high blood pressure caused by pre eclampsia - labetalol is 1st line

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137
Q

what complications can beta blockers cause in pregnancy

A

Fetal growth restriction
Hypoglycaemia in the neonate
Bradycardia in the neonate

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138
Q

what is the effect of taking ACEi/ARBs in pregnancy

A

they can reduce the production of urine in the fetus, as well as hypocalvaria which is the incomplete formation of the skull bones. Use can also cause:
Oligohydramnios (reduced amniotic fluid)
Miscarriage or fetal death
Renal failure in the neonate
Hypotension in the neonate

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139
Q

what can use of opiates in pregnancy cause in the fetus

A

withdrawal symptoms in the neonate after birth. This is called neonatal abstinence syndrome (NAS). NAS presents between 3 – 72 hours after birth with irritability, tachypnoea (fast breathing), high temperatures and poor feeding.

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140
Q

is warfarin used in pregnancy

A

no it is considered teratogenic, it can cause:
Fetal loss
Congenital malformations, particularly craniofacial problems
Bleeding during pregnancy, postpartum haemorrhage, fetal haemorrhage and intracranial bleeding

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141
Q

what can use of sodium valproate cause in pregnancy

A

neural tube defects and developmental delay.

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142
Q

is lithium used in pregnancy

A

it is avoided in pregnant women or those planning on getting pregnant
- avoided particularly in the 1st trimester as it is linked to congenital cardiac abnormalities particularly Ebsteins anomaly

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143
Q

are SSRIs used in pregnancy

A

the risks need to be balanced against the benefits, as there are side effects in pregnancy:
First-trimester use has a link with congenital heart defects
First-trimester use of paroxetine has a stronger link with congenital malformations
Third-trimester use has a link with persistent pulmonary hypertension in the neonate
Neonates can experience withdrawal symptoms, usually only mild and not requiring medical management

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144
Q

what is isotretinoin and can it be used in pregnancy

A

it is a retinoid medication and is used to treat severe acne
it is highly teratogenic and women taking it should be on very reliable contraception before, during and for one month after

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145
Q

should women be given the MMR vaccine during pregnancy

A

NO - pregnant women shouldnt receive live vaccines

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146
Q

what can ZVZ cause if contraced

A

More severe cases in the mother, such as varicella pneumonitis, hepatitis or encephalitis
Fetal varicella syndrome
Severe neonatal varicella infection (if infected around delivery)

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147
Q

what should be done if a women has exposure to VZV in pregnancy

A

When the pregnant woman has previously had chickenpox, they are safe
When they are not sure about their immunity, test the VZV IgG levels. If positive, they are safe.
When they are not immune, they can be treated with IV varicella immunoglobulins as prophylaxis against developing chickenpox. This should be given within ten days of exposure.

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148
Q

what should be done if a woman develops a chicken pox rash in pregnancy

A

oral aciclovir if they present within 24 hours and are more than 20 weeks gestation

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149
Q

what are the features of congenital varicella syndrome

A

Fetal growth restriction
Microcephaly, hydrocephalus and learning disability
Scars and significant skin changes located in specific dermatomes
Limb hypoplasia (underdeveloped limbs)
Cataracts and inflammation in the eye (chorioretinitis)

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150
Q

what are the risks of listeria infection in pregnancy

A

high rate of miscarriage or fetal death. It can also cause severe neonatal infection.

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151
Q

what are the features of congenital CMV

A

Fetal growth restriction
Microcephaly
Hearing loss
Vision loss
Learning disability
Seizures

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152
Q

what is the classic triad of congenital toxoplasmosis

A

infection caused by toxoplasma gondii causes:
Intracranial calcification
Hydrocephalus
Chorioretinitis (inflammation of the choroid and retina in the eye)

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153
Q

what are the complications of contracting parvovirus B19 in pregnancy

A

can lead to several complications, particularly in the first and second trimesters. Complications are:
Miscarriage or fetal death
Severe fetal anaemia caused by infection of the erythroid progenitor cells in the bone marrow/liver
Hydrops fetalis (fetal heart failure)
Maternal pre-eclampsia-like syndrome - mirror syndrome

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154
Q

what should be done in pregnant women with suspected parvovirus infection

A

Women suspected of parvovirus infection need tests for:
IgM to parvovirus, which tests for acute infection within the past four weeks
IgG to parvovirus, which tests for long term immunity to the virus after a previous infection
Rubella antibodies (as a differential diagnosis)

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155
Q

what are the symptoms of congenital zika syndrome

A

Microcephaly
Fetal growth restriction
Other intracranial abnormalities, such as ventriculomegaly and cerebellar atrophy

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156
Q

what is the pathophysiology of resus incompatibility in pregnancy

A

When a woman that is rhesus-D negative becomes pregnant, we have to consider the possibility that her child will be rhesus positive
Fetal blood will be exposed to the mothers circulation and the mother will be primed/sensitised to the rhesus D antigens
usually this doesnt cause issues in the first pregnancy, however subsequent pregnancies the mothers anti D antibodies can cross the placenta. If the fetus is rhesus positive these antibodies will attack the babies red blood cells. This is called haemolytic disease of the newborn

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157
Q

what is the management of rhesus incompatibility in pregnancy

A

IM anti-D injections given to rhesus negative mothers which works by attaching itself to the rhesus antigens and cause them to be destroyed.

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158
Q

when are Anti-D injections given in pregnancy

A

Anti-D injections are given routinely on two occasions:
28 weeks gestation
Birth (if the baby’s blood group is found to be rhesus-positive)

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159
Q

what points are anti-D injections also given in pregnancy beside the routine occasions

A

Anti-D injections should also be given at any time where sensitisation may occur, such as:
Antepartum haemorrhage
Amniocentesis procedures
Abdominal trauma
- given within 72 hours of sensitisation event

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160
Q

what is the kleihauer test

A

it is a check of how much fetal blood has passed into the mothers during a sensitisation event (after 20 weeks)
- adding acid to a sample of mothers blood, and as fetal haemoglobin is more resistant to acid it persists in response to the added acid while maternal blood is destroyed

161
Q

what is a small for gestational age fetus

A

it is measures below the 10th centile

162
Q

what two measurements on ultrasound are used to assess fetal size

A

estimated fetal weight
fetal abdominal circumference

163
Q

what parameters are used to produce a customised growth chart

A

ethnic group
weight
height
parity

164
Q

what is defined as severe growth restriction

A

then the fetus is below the 3rd centile for their gestational age

165
Q

what is low birth weight defined as

A

a birth weight of less than 2500g

166
Q

what are the two categories for causes of small for gestational age

A

Constitutionally small, matching the mother and others in the family, and growing appropriately on the growth chart
Fetal growth restriction (FGR), also known as intrauterine growth restriction (IUGR)

167
Q

what is the difference between small for gestational age and fetal growth restriction

A

Small for gestational age simply means that the baby is small for the dates, without stating why. The fetus may be constitutionally small, growing appropriately, and not at increased risk of complications. Alternatively, the fetus may be small for gestational age due to pathology (i.e. FGR), with a higher risk of morbidity and mortality.

168
Q

what are the two categories for causes of fetal growth restriction

A

Placenta mediated growth restriction
Non-placenta mediated growth restriction, where the baby is small due to a genetic or structural abnormality

169
Q

what are placenta mediated causes of growth restriction in a fetus

A

Idiopathic
Pre-eclampsia
Maternal smoking
Maternal alcohol
Anaemia
Malnutrition
Infection
Maternal health conditions

170
Q

what are non placental mediated causes for growth restriction

A

Genetic abnormalities
Structural abnormalities
Fetal infection
Errors of metabolism

171
Q

what are signs that indicate fetal growth restriction

A

Reduced amniotic fluid volume
Abnormal Doppler studies
Reduced fetal movements
Abnormal CTGs

172
Q

what are complications of fetal growth restriction

A

Fetal death or stillbirth
Birth asphyxia
Neonatal hypothermia
Neonatal hypoglycaemia
long term complications include: CVD (hypertension), type 2 diabetes, obesity and mood and behavioural problems

173
Q

what are risk factors for small for gestational age

A

Previous SGA baby
Obesity
Smoking
Diabetes
Existing hypertension
Pre-eclampsia
Older mother (over 35 years)
Multiple pregnancy
Low pregnancy‑associated plasma protein‑A (PAPPA)
Antepartum haemorrhage
Antiphospholipid syndrome

174
Q

how are small for gestational age babies monitored

A

there are RCOG green top guidelines which lists major and minor risk factors and these are assessed at booking clinic
- low risk women have monitoring of the symphysis fundal height at every antenatal appointment for 24 weeks
- if the symphysis fundal height is less than the 10th centile, women are booked for serial growth scans with umbilical artery doppler

175
Q

when are women booked for serial growth scans with umbilical artery doppler

A

if they have:
Three or more minor risk factors
One or more major risk factors
Issues with measuring the symphysis fundal height (e.g. large fibroids or BMI > 35)

176
Q

women who are at risk of small for gestational age or have a small for gestation age baby what is measured during serial ultrasound scans

A

Estimated fetal weight (EFW) and abdominal circumference (AC) to determine the growth velocity
Umbilical arterial pulsatility index (UA-PI) to measure flow through the umbilical artery
Amniotic fluid volume

177
Q

what are the critical steps for managing small for gestational age

A

Identifying those at risk of SGA
Aspirin is given to those at risk of pre-eclampsia
Treating modifiable risk factors (e.g. stop smoking)
Serial growth scans to monitor growth
Early delivery where growth is static, or there are other concerns

178
Q

what investigations should be done if a fetus is identified as small for gestational age

A

Blood pressure and urine dipstick for pre-eclampsia
Uterine artery doppler scanning
Detailed fetal anatomy scan by fetal medicine
Karyotyping for chromosomal abnormalities
Testing for infections (e.g. toxoplasmosis, cytomegalovirus, syphilis and malaria)

179
Q

when are babies defined as large for gestation age

A

when the weight of the newborn is more than 4.5 kg at birth or if the estimated fetal weight is above the 90th centile

180
Q

what are causes of macrosomia (LGA)

A

Constitutional
Maternal diabetes
Previous macrosomia
Maternal obesity or rapid weight gain
Overdue
Male baby

181
Q

what are the risks of macrosomia (LGA)on the mother

A

Shoulder dystocia
Failure to progress
Perineal tears
Instrumental delivery or caesarean
Postpartum haemorrhage
Uterine rupture (rare)

182
Q

what are risks of macrosomia (LGA) to the baby

A

Birth injury (Erbs palsy, clavicular fracture, fetal distress and hypoxia)
Neonatal hypoglycaemia
Obesity in childhood and later life
Type 2 diabetes in adulthood

183
Q

what is the management of macrosomia (LGA)

A

ultrasounds are done to exclude polyhydramnios and estimate fetal weight
OGTT for gestational diabetes
reduce risks of shoulder dystocia by having delivery on a consultant lead unit with experienced midwives, access to theatre, active management of the third stage, early decision for caesarean.
NICE (2008) advise against induction of labour only on the grounds of macrosomia

184
Q

what are the types of multiple pregnancy

A

Monozygotic - identical twins
Dizygotic - non identical twins
Monoamniotic - when they share one sac
Diamniotic - two separate amniotic sacs
monochorionic - share a single placenta
dichorionic - two separate placentas

185
Q

what is the best outcomes for twins in terms of the amniotic sac and placenta

A

when there is two amniotic sacs and two placentas as each fetus will have its own nutrient supply

186
Q

how do you determine the type of twins on an ultrasound scan

A

Dichorionic diamniotic twins have a membrane between the twins, with a lambda sign or twin peak sign
Monochorionic diamniotic twins have a membrane between the twins, with a T sign
Monochorionic monoamniotic twins have no membrane separating the twins

187
Q

what is the lambda/twin peak sign

A

it refers to a triangular appearance where the membrane between the twins meets the chorion, as the chorion blends partially into the membrane. This indicates a dichorionic twin pregnancy (separate placentas).

188
Q

what does the T sign indicate in twins

A

The T sign refers to where the membrane between the twins abruptly meets the chorion, giving a T appearance. This indicates a monochorionic twin pregnancy (single placenta).

189
Q

what are risks of twins to the mother

A

Anaemia
Polyhydramnios
Hypertension
Malpresentation
Spontaneous preterm birth
Instrumental delivery or caesarean
Postpartum haemorrhage

190
Q

what are the risk of having twins to the fetuses and neonates

A

Miscarriage
Stillbirth
Fetal growth restriction
Prematurity
Twin-twin transfusion syndrome
Twin anaemia polycythaemia sequence
Congenital abnormalities

191
Q

what is twin twin transfusion syndrome

A

this is when fetuses share one placenta
one fetus may receive the majority of the blood (recipient) while the other (donor) is starved of blood
the recipient gets more blood and is at risk of fluid overload with heart failure and polyhydramnios
the donor is at risk of growth restriction, anaemia and oligohydramnios

192
Q

what is twin anaemia polycythaemia sequence

A

Twin anaemia polycythaemia sequence is similar to twin-twin transfusion syndrome, but less acute. One twin becomes anaemic whilst the other develops polycythaemia (raised haemoglobin).

193
Q

how are twins managed antenatally

A

Women with multiple pregnancies require additional monitoring for anaemia, with a full blood count at: Booking clinic, 20 weeks gestation, 28 weeks gestation
Additional ultrasound scans are required in multiple pregnancy to monitor for fetal growth restriction, unequal growth and twin-twin transfusion syndrome: 2 weekly scans from 16 weeks for monochorionic twins, 4 weekly scans from 20 weeks for dichorionic twins

194
Q

when is the birth planned for twins

A

32 and 33 + 6 weeks for uncomplicated monochorionic monoamniotic twins
36 and 36 + 6 weeks for uncomplicated monochorionic diamniotic twins
37 and 37 + 6 weeks for uncomplicated dichorionic diamniotic twins
Before 35 + 6 weeks for triplets

195
Q

how are twins delivered

A

Monoamniotic twins require elective caesarean section at between 32 and 33 + 6 weeks.
Diamniotic twins (aim to deliver between 37 and 37 + 6 weeks):
Vaginal delivery is possible when the first baby has a cephalic presentation (head first)
Caesarean section may be required for the second baby after successful birth of the first baby
Elective caesarean is advised when the presenting twin is not cephalic presentation

196
Q

what does UTI in pregnant women increase the risk of

A

preterm delivery
low birth weight
pre-eclampsia

197
Q

what is asymptomatic bacteriuria

A

bacteria present in the urine, without symptoms of infection. Pregnant women with asymptomatic bacteriuria are at higher risk of developing lower urinary tract infections and pyelonephritis, and subsequently at risk of preterm birth.

198
Q

when is asymptomatic bacteriuria tested for in pregnancy

A

during booking clinic and routinely throughout pregnancy

199
Q

what are common causes of UTI

A

most common = E.coli
Klebsiella pneumoniae (gram-negative anaerobic rod)
Enterococcus
Pseudomonas aeruginosa
Staphylococcus saprophyticus
Candida albicans (fungal)

200
Q

what is the management of UTI in pregnancy

A

Urinary tract infection in pregnancy requires 7 days of antibiotics.
The antibiotic options are:
Nitrofurantoin (avoid in the third trimester due to risk of neonatal haemolysis)
Amoxicillin (only after sensitivities are known)
Cefalexin
- trimethoprim must be avoided in the first trimester as it is a folate antagonist therefore can cause congenital malformations (neural tube defects)

201
Q

when are women screened for anaemia in pregnancy

A

Booking clinic
28 weeks gestation

202
Q

what are the normal ranges for haemaglobin during pregnancy

A

booking bloods >110g/l
28 weeks >105g/l
post partum >100g/l

203
Q

what is the management for women who have iron deficiency anaemia in pregnancy

A

Women with anaemia in pregnancy are started on iron replacement (e.g. ferrous sulphate 200mg three times daily). When women are not anaemic, but have a low ferritin (indicating low iron stores), they may be started on supplementary iron.

204
Q

what is done in women with low B12 in pregnancy

A

increased plasma volume and B12 requirements in pregnancy can result in low B12
- women with low B12 should be tested for pernicious anaemia
- if B12 is low: IM hydroxocobalamin injections or oral cyanocobalamin tablets

205
Q

what are risk factors for developing a VTE in pregnancy

A

Smoking
Parity ≥ 3
Age > 35 years
BMI > 30
Reduced mobility
Multiple pregnancy
Pre-eclampsia
Gross varicose veins
Immobility
Family history of VTE
Thrombophilia
IVF pregnancy

206
Q

in women with VTE risk factors what is the management

A

The RCOG guidelines (2015) advise starting prophylaxis from:
28 weeks if there are three risk factors
First trimester if there are four or more of these risk factors
women are given low molecular weight heparin (enoxaparin, dalteparin, tinzaparin)

207
Q

what other mechanical prophylaxis may be given in pregnancy if low molecular weight heparin is contraindicated

A

Intermittent pneumatic compression with equipment that inflates and deflates to massage the legs
Anti-embolic compression stockings

208
Q

what is the management of a pregnant women who has presented with VTE or PE

A

VTE: LMWH started immediately, before confirming the diagnosis. If it is confirmed then LMWH is continued for the remainder of pregnancy and 6 weeks postnatally or three months in total (whichever is loner)
PE: Unfractionated heparin, thrombolysis, surgical embolectomy

209
Q

what is pre-eclampsia

A

Pre-eclampsia refers to new high blood pressure (hypertension) in pregnancy with end-organ dysfunction, notably with proteinuria (protein in the urine). It occurs after 20 weeks gestation, when the spiral arteries of the placenta form abnormally, leading to a high vascular resistance in these vessels.

210
Q

what is the pathophysiology of pre-eclampsia

A

when the process of forming the lacunae is inadequate, the woman can develop pre-eclampsia
there is high vascular resistance in the spiral arteries causing poor perfusion of the placenta. this causes oxidative stress and relieve of inflammatory chemicals into the systemic circulation, leading to systemic inflammation and impaired endothelial function

211
Q

what are high risk factors for developing pre-eclampsia

A

Pre-existing hypertension
Previous hypertension in pregnancy
Existing autoimmune conditions (e.g. systemic lupus erythematosus)
Diabetes
Chronic kidney disease

212
Q

what are the moderate risk factors for developing pre-eclampsia

A

Older than 40
BMI > 35
More than 10 years since previous pregnancy
Multiple pregnancy
First pregnancy
Family history of pre-eclampsia

213
Q

how is pre-eclampsia defined

A

systolic over 140, diastolic over 90
plus: proteinuria, or organ dysfunction or placental dysfunction

214
Q

what is the prophylaxis for pre-eclampsia

A

aspirin given from 12 weeks gestation until birth to women with:
a single high risk factor
two or more moderate risk factor

215
Q

what is the medical management of pre-eclampsia

A

Labetolol is first-line as an antihypertensive
Nifedipine (modified-release) is commonly used second-line
Methyldopa is used third-line (needs to be stopped within two days of birth)
Intravenous hydralazine may be used as an antihypertensive in critical care in severe pre-eclampsia or eclampsia
IV magnesium sulphate is given during labour and in the 24 hours afterwards to prevent seizures
Fluid restriction is used during labour in severe pre-eclampsia or eclampsia, to avoid fluid overload

216
Q

what is the most significant immediate complication of gestational diabetes

A

large for dates fetus and macrosomia
- shoulder distocia

217
Q

what are risk factors for the development of gestational diabetes

A

The NICE guidelines (2015) list the risk factors that warrant testing for gestational diabetes:
Previous gestational diabetes
Previous macrosomic baby (≥ 4.5kg)
BMI > 30
Ethnic origin (black Caribbean, Middle Eastern and South Asian)
Family history of diabetes (first-degree relative)

218
Q

Which mothers is the OGTT used to test for gestational diabetes

A

An OGTT is used in patients with risk factors for gestational diabetes, and also when there are features that suggest gestational diabetes:
Large for dates fetus
Polyhydramnios (increased amniotic fluid)
Glucose on urine dipstick

219
Q

when is the OGTT given in pregnancy

A

between weeks 24-28

220
Q

how is the OGTT performed

A

An OGTT should be performed in the morning after a fast (they can drink plain water). The patient drinks a 75g glucose drink at the start of the test. The blood sugar level is measured before the sugar drink (fasting) and then at 2 hours.
Normal results are:
Fasting: < 5.6 mmol/l
At 2 hours: < 7.8 mmol/l
Results higher than these values are used to diagnose gestational diabetes.

221
Q

what is the management of gestational diabetes

A
  1. 4 weekly ultrasound scans to monitor fetal growth and amniotic fluid level from 28 -36 weeks
  2. if the fasting is less than 7, trial of diet and exercise for 1-2 weeks, followed by metformin, then insulin
  3. if fasting glucose is above 7 start insulin +/- metformin
  4. same as above in fasting glucose over 6 plus macrosomia
  5. glibenclamide (sulfonylurea) is used if metformin isnt tolerated and insulin is refused
222
Q

what are the target levels for blood glucose a woman with gestational diabetes should aim for

A

The NICE (2015) target levels are:
Fasting: 5.3 mmol/l
1 hour post-meal: 7.8 mmol/l
2 hours post-meal: 6.4 mmol/l
Avoiding levels of 4 mmol/l or below

223
Q

what dose of folic acid should women with pre-existing diabetes be given in pregnancy

A

5mg

224
Q

how are women with pre-existing type 2 diabetes managed in pregnancy

A

with insulin and metformin, all other oral diabetic medications are stopped

225
Q

what screening is very important to do in pregnancy with women who have pre-existing diabetes

A

retinopathy screening - performed after booking and at 28 weeks gestation

226
Q

when should women with pre-existing diabetes give birth

A

NICE (2015) advise a planned delivery between 37 and 38 + 6 weeks for women with pre-existing diabetes
- sliding scale insulin regime is considered during labour for women with T1DM (mix of dextrose and insulin)

227
Q

what are babies of mothers with diabetes at risk of

A

Neonatal hypoglycaemia
Polycythaemia (raised haemoglobin)
Jaundice (raised bilirubin)
Congenital heart disease
Cardiomyopathy

228
Q

what blood glucose level should babies be maintained at

A

The aim is to maintain their blood sugar above 2 mmol/l, and if it falls below this, they may need IV dextrose of nasogastric feeding.

229
Q

what is obstetric cholestasis

A

it is the reduced outflow of bile acids from the liver during pregnancy thought to be due to increased oestrogen and progesterone

230
Q

what risk is obstetric cholestasis associated with

A

increased risk of stillbirth

231
Q

how does obstetric cholestasis present

A

later in pregnancy - third trimester
itching - main symptom
fatigue
dark urine
pale greasy stools
jaundice
NO RASH

232
Q

what investigations should be done on women with suspected obstetric cholestasis

A

Liver function tests and bile acid checks
- Abnormal LFT: AST, ALT, GGT
- raised bile acids

233
Q

what is the management of obstetric cholestasis

A

Emollients to soothe skin
antihistamines to help sleeping
Water soluble vitamin K may be considered if clotting is deranged
if bile acids and LFTs are severely deranged planned delivery is considered

234
Q

what is acute fatty liver of pregnancy

A

rare condition that occurs in the third trimester of pregnancy. There is a rapid accumulation of fat within the liver cells (hepatocytes), causing acute hepatitis. There is a high risk of liver failure and mortality, for both the mother and fetus.

235
Q

what is the pathophysiology of acute fatty liver

A

impaired processing of atty acids in the placenta as a result of a genetic condition in the fetus which impairs fatty acid metabolism (LCHAD deficiency)
this enzyme is important in fatty acid oxidation, and the unbroken fatty acids enter the mother circulation and accumulate in the liver

236
Q

how does acute fatty liver of pregnancy present

A

General malaise and fatigue
Nausea and vomiting
Jaundice
Abdominal pain
Anorexia (lack of appetite)
Ascites

237
Q

what might blood show in acute fatty liver of pregnancy

A

Liver function tests will show elevated liver enzymes (ALT and AST).
Other bloods may be deranged, with:
Raised bilirubin
Raised WBC count
Deranged clotting (raised prothrombin time and INR)
Low platelets

238
Q

what is the management of acute fatty liver of pregnancy

A

obstetric emergency and requires prompt admission and delivery of the baby. Most patients will recover after delivery.
Management also involves treatment of acute liver failure if it occurs, including consideration of liver transplant.

239
Q

what is polymorphic eruption of pregnancy

A

it is pruritic and urticarial papules and plaques in the third trimester - usually begins on the abdomen and is associated with stretch marks
it is characterised by urticarial papules, wheals (itch areas of skin) and plaques

240
Q

how is polymorphic eruption of pregnancy managed

A

Topical emollients
Topical steroids
Oral antihistamines
Oral steroids may be used in severe cases

241
Q

what is atopic eruption of pregnancy

A

this is essentially eczema which flares up during pregnancy
usually presents in the first and second trimester
- E type: eczema type - inflamed, red, itchy skin
- P type: prurigo type- intensely itchy papules typically affecting abdomen, back and limbs

242
Q

what is the management of atopic eruption of pregnancy

A

Topical emollients
Topical steroids
Phototherapy with ultraviolet light (UVB) may be used in severe cases
Oral steroids may be used in severe cases

243
Q

what is melasma

A

it is increased pigmentation to patches of the skin on the face during pregnancy
it is usually symmetrical, flat and affects sun exposed areas

244
Q

what is melasma associated with

A

sun exposure, thyroid disease and family history.

245
Q

what is the management of melasma

A

Avoiding sun exposure and using suncream
Makeup (camouflage)
Skin lightening cream (e.g. hydroquinone or retinoid creams), although not in pregnancy and only under specialist care
Procedures such as chemical peels or laser treatment (not usually on the NHS)

246
Q

what is pyogenic granuloma

A

this is also known as lobar capillary haemangioma and is a benign rapidly growing tumour of capillaries presenting as a discrete lump with a dark or red appearance.
- develops over days up to 1-2 cm in size and often occur on the fingers, upper chest, back, head or neck

247
Q

how are pyogenic granulomas managed

A

When they occur in pregnancy, they usually resolve without treatment after delivery. Treatment is with surgical removal with histology to confirm the diagnosis.

248
Q

what is pemphigoid gestationis

A

rare autoimmune skin condition that occurs in pregnancy where autoantibodies are created which damage the connection between the dermis and epidermis causing them to separate and creating a space that can fill with fluid (large, fluid filled blisters - bullae)
- typically occurs in second or third trimester as a itchy red papular or blistering rash around umbilicus which then spreads to other parts of the body

249
Q

what are the risks to the fetus in pemphigoid gestationis

A

Fetal growth restriction
Preterm delivery
Blistering rash after delivery (as the maternal antibodies pass to the baby)

249
Q

what is the treatment for pemphigoid gestationis

A

Topical emollients
Topical steroids
Oral steroids may be required in severe cases
Immunosuppressants may be required where steroids are inadequate
Antibiotics may be necessary if infection occurs

250
Q

what is the difference between low lying placenta and placental praevia

A

Low-lying placenta is used when the placenta is within 20mm of the internal cervical os
Placenta praevia is used only when the placenta is over the internal cervical os

251
Q

what are the risks of placental praevia on the mother

A

Antepartum haemorrhage
Emergency caesarean section
Emergency hysterectomy
Maternal anaemia and transfusions
Preterm birth and low birth weight
Stillbirth

252
Q

what re the grades of placenta praevia

A

Minor praevia, or grade I – the placenta is in the lower uterus but not reaching the internal cervical os
Marginal praevia, or grade II – the placenta is reaching, but not covering, the internal cervical os
Partial praevia, or grade III – the placenta is partially covering the internal cervical os
Complete praevia, or grade IV – the placenta is completely covering the internal cervical os

253
Q

what are the risk factors for developing placenta praevia

A

Previous caesarean sections
Previous placenta praevia
Older maternal age
Maternal smoking
Structural uterine abnormalities (e.g. fibroids)
Assisted reproduction (e.g. IVF)

254
Q

what is the management of placental praevia

A

those diagnosed early (20 week scan) will require a repeat transvaginal ultrasound scan at 32 and 36 weeks
corticosteroids should be given at 34 and 35+6 weeks
delivery is planned between 36 and 37 weeks with a planned caesarean section

255
Q

what is vasa praevia

A

a condition where the fetal vessels are within the fetal membranes (chorioamniotic membranes) and travel across the internal cervical os.

256
Q

what are the two instances when the fetal vessels can be exposed outside the protection of the umbilical cord or placenta

A

Velamentous umbilical cord is where the umbilical cord inserts into the chorioamniotic membranes, and the fetal vessels travel unprotected through the membranes before joining the placenta.
An accessory lobe of the placenta (also known as a succenturiate lobe) is connected by fetal vessels that travel through the chorioamniotic membranes between the placental lobes.

257
Q

what are the two types of vasa praevia

A

Type I vasa praevia – the fetal vessels are exposed as a velamentous umbilical cord
Type II vasa praevia – the fetal vessels are exposed as they travel to an accessory placental lobe

258
Q

what are the risk factors for vasa praevia

A

Low lying placenta
IVF pregnancy
Multiple pregnancy

259
Q

what is the management of vasa praevia

A

Corticosteroids, given from 32 weeks gestation to mature the fetal lungs
Elective caesarean section, planned for 34 – 36 weeks gestation
if antepartum haemorrhage occurs emergency caesarean section is required

260
Q

what is placental abruption

A

when the placenta separates from the wall of the uterus during pregnancy

261
Q

what are the risk factors for placental abruption

A

Previous placental abruption
Pre-eclampsia
Bleeding early in pregnancy
Trauma (consider domestic violence)
Multiple pregnancy
Fetal growth restriction
Multigravida
Increased maternal age
Smoking
Cocaine or amphetamine use

262
Q

how does placental abruption present

A

Sudden onset severe abdominal pain that is continuous
Vaginal bleeding (antepartum haemorrhage)
Shock (hypotension and tachycardia)
Abnormalities on the CTG indicating fetal distress
Characteristic “woody” abdomen on palpation, suggesting a large haemorrhage

263
Q

what is the classification of a minor, major and massive antepartum haemorrhage in pregnancy

A

Minor haemorrhage: less than 50ml blood loss
Major haemorrhage: 50 – 1000ml blood loss
Massive haemorrhage: more than 1000 ml blood loss, or signs of shock

264
Q

what is the management for placental abruption

A

obstetric emergency - important to consider concealed haemorrhage as well
Urgent involvement of a senior obstetrician, midwife and anaesthetist
2 x grey cannula
Bloods include FBC, UE, LFT and coagulation studies
Crossmatch 4 units of blood
Fluid and blood resuscitation as required
CTG monitoring of the fetus
Close monitoring of the mother
steroids to mature fetal lungs + anti-D in rhesus negative women
emergency caesarean

265
Q

what is placental accreta

A

it is when the placental implants deeper through and past the endometrium

266
Q

what are the three definitions of placenta accreta depending on the depth of insertion

A

Superficial placenta accreta is where the placenta implants in the surface of the myometrium, but not beyond
Placenta increta is where the placenta attaches deeply into the myometrium
Placenta percreta is where the placenta invades past the myometrium and perimetrium, potentially reaching other organs such as the bladder

267
Q

what are risk factors for placenta accreta

A

Previous placenta accreta
Previous endometrial curettage procedures (e.g. for miscarriage or abortion)
Previous caesarean section
Multigravida
Increased maternal age
Low-lying placenta or placenta praevia

268
Q

how does placental accreta present

A

It can present with bleeding (antepartum haemorrhage) in the third trimester
It may be diagnosed on antenatal ultrasound scans
It may be diagnosed at birth, when it becomes difficult to deliver the placenta. It is a cause of significant postpartum haemorrhage.

269
Q

how is placenta accreta managed

A

MDT approach - additional management at birth due to risk of bleeding: complex uterine surgery, blood transfusions, intensive care for the mother, neonatal intensive care
delivery is planned between 35-36+6 weeks
steroids are given to mature fetal lungs
options during surgery are: hysterectomy, uterus preserving surgery, expectant management

270
Q

what are the types of breech presentation

A
  1. Complete breech, where the legs are fully flexed at the hips and knees
  2. Incomplete breech, with one leg flexed at the hip and extended at the knee
  3. Extended breech, also known as frank breech, with both legs flexed at the hip and extended at the knee
  4. Footling breech, with a foot is presenting through the cervix with the leg extended
271
Q

what is the management of breech babies

A

those breech before 36 weeks often turn spontaneously
External cephalic version can be used at 37 weeks to attempt to turn the baby
if ECV fails women can do a vaginal delivery (safer for mother), or elective caesarean section (safer for baby)

272
Q

how does external cephalic version work

A

this is a technique used to attempt to turn a fetus it is about 50% successful
- women are given tocolysis to relax the uterus before the procedure (terbutaline)
- it is done after 36 weeks for nulliparous women and after 37 weeks for women who have given birth previously
- Rhesus negative women require anti-D prophylaxis and a kleihauer test is used to quantify exposure of the mother to fetal blood

273
Q

what are causes of stillbirth

A

Unexplained (around 50%)
Pre-eclampsia
Placental abruption
Vasa praevia
Cord prolapse or wrapped around the fetal neck
Obstetric cholestasis
Diabetes
Thyroid disease
Infections, such as rubella, parvovirus and listeria
Genetic abnormalities or congenital malformations

274
Q

what factors increase the risk of stillbirth

A

Fetal growth restriction
Smoking
Alcohol
Increased maternal age
Maternal obesity
Twins
Sleeping on the back (as opposed to either side)
having risk factors for small for gestational age

275
Q

what are three key symptoms of stillbirth that should always be asked during pregnancy

A

Reduced fetal movements
Abdominal pain
Vaginal bleeding

276
Q

how is stillbirth diagnosed and managed

A

ultrasound scan
- vaginal birth is first line for most women after IUFD, with either induction or expectant management
Dopamine agonists can be used to suppress lactation after stillbirth

277
Q

what testing can be carried out after stillbirth to determine cause

A

Genetic testing of the fetus and placenta
Postmortem examination of the fetus (including xrays)
Testing for maternal and fetal infection
Testing the mother for conditions associated with stillbirth, such as diabetes, thyroid disease and thrombophilia

278
Q

what are the reversible causes of adult cardiac arrest

A

4Ts and 4Hs:
Thrombosis (i.e. PE or MI)
Tension pneumothorax
Toxins
Tamponade (cardiac)
Hypoxia
Hypovolaemia
Hypothermia
Hyperkalaemia, hypoglycaemia, and other metabolic abnormalities
- also add eclampsia and intracranial haemorrhage

279
Q

what are the three major causes of cardiac arrest in pregnancy

A

Obstetric haemorrhage
Pulmonary embolism
Sepsis leading to metabolic acidosis and septic shock

280
Q

what is aortocaval compression

A

after 20 weeks gestation the uterus is a significant size, when a woman lies on her back the mass of the uterus can compress the inferior vena cava and aorta reducing blood returning to the heart - reduces CO and causes hypotension
this can be enough to lead to loss of CO and cause cardiac arrest

281
Q

how is resuscitation done in pregnancy

A

A 15 degree tilt to the left side for CPR, to relieve compression of the inferior vena cava and aorta
Early intubation to protect the airway
Early supplementary oxygen
Aggressive fluid resuscitation (caution in pre-eclampsia)
Delivery of the baby after 4 minutes, and within 5 minutes of starting CPR

282
Q

what prophylaxis can be done for preterm labour

A

vaginal progesterone (prevents the cervix remodelling in preparation for deliver) - offered between 16-24 weeks
cervical cerclage - offered between 16-24 weeks who had previous premature birth or cervical trauma

283
Q

if there is doubt is membranes have ruptured what tests can be performed

A

Insulin-like growth factor-binding protein-1 (IGFBP-1) is a protein present in high concentrations in amniotic fluid, which can be tested on vaginal fluid if there is doubt about rupture of membranes
Placental alpha-microglobin-1 (PAMG-1) is a similar alternative to IGFBP-1

284
Q

what is fetal fibronectin

A

alternative test to vaginal ultrasound. Fetal fibronectin is the “glue” between the chorion and the uterus, and is found in the vagina during labour. A result of less than 50 ng/ml is considered negative, and indicates that preterm labour is unlikely.

285
Q

what are options which can be used to improve the outcome of preterm labour

A

Fetal monitoring (CTG or intermittent auscultation)
Tocolysis with nifedipine: nifedipine is a calcium channel blocker that suppresses labour
Maternal corticosteroids: can be offered before 35 weeks gestation to reduce neonatal morbidity and mortality
IV magnesium sulphate: can be given before 34 weeks gestation and helps protect the baby’s brain
Delayed cord clamping or cord milking: can increase the circulating blood volume and haemoglobin in the baby at birth

286
Q

what situations would it be beneficial to induce labour early

A

Prelabour rupture of membranes
Fetal growth restriction
Pre-eclampsia
Obstetric cholestasis
Existing diabetes
Intrauterine fetal death

287
Q

what is the bishop score

A

The Bishop score is a scoring system used to determine whether to induce labour.
Five things are assessed and given a score based on different criteria (minimum score is 0 and maximum is 13):
Fetal station (scored 0 – 3)
Cervical position (scored 0 – 2)
Cervical dilatation (scored 0 – 3)
Cervical effacement (scored 0 – 3)
Cervical consistency (scored 0 – 2)

288
Q

what are the options for induction of labour

A

membrane sweep - at 40 weeks to initiate labour
vaginal prostaglandin E2 - pessary/gel/tablet
cervical ripening balloon - used when prostaglandins arent preferred
artificial rupture of membranes - only when there are reasons not to use prostaglandins
oral mifepristone plus misoprostol - where intrauterine fetal death has occurred

289
Q

what are the two means of monitoring during labour

A

Cardiotocography (CTG) to assess the fetal heart rate and uterine contractions before and during induction of labour
Bishop score before and during induction of labour to monitor the progress

290
Q

what is uterine hyperstimulation

A

it is the main complication of induction of labour with vaginal prostaglandins - where the contraction of the uterus is prolonged and frequent causing fetal distress and compromise
- lasting longer than 2 minutes
- more than 5 uterine contractions every 10 minutes

291
Q

what is the management of uterine rupture

A

Removing the vaginal prostaglandins, or stopping the oxytocin infusion
Tocolysis with terbutaline
caesarean and surgery to repair uterus

292
Q

what two factors are measured to get the CTG readout

A

One above the fetal heart to monitor the fetal heartbeat
One near the fundus of the uterus to monitor the uterine contractions

293
Q

what are indications for continuous CTG monitoring

A

Sepsis
Maternal tachycardia (> 120)
Significant meconium
Pre-eclampsia (particularly blood pressure > 160 / 110)
Fresh antepartum haemorrhage
Delay in labour
Use of oxytocin
Disproportionate maternal pain

294
Q

what are the 5 key features to look at on a CTG

A
  1. Contractions – the number of uterine contractions per 10 minutes
  2. Baseline rate – the baseline fetal heart rate
  3. Variability – how the fetal heart rate varies up and down around the baseline
  4. Accelerations – periods where the fetal heart rate spikes
  5. Decelerations – periods where the fetal heart rate drops
295
Q

what are reassuring, non reassuring and abnormal baseline rates and variability on CTG

A
  1. Reassuring - 110-160 variability 5-25
  2. non reassuring - 100-109 or 161-180 variability less than 5 for 30-50 minutes or more than 25 for 15-25 minutes
  3. abnormal - below 100, over 180, variability less than 5 for over 50 minutes or more than 25 for over 25 minutes
296
Q

what are the four types of decelerations on CTG

A

Early decelerations
Late decelerations
Variable decelerations
Prolonged decelerations

297
Q

what are early decelerations

A

gradual dips and recoveries in heart rate that correspond with uterine contractions. The lowest point of the declaration corresponds to the peak of the contraction. Early decelerations are normal and not considered pathological

298
Q

what are late decelerations

A

gradual falls in heart rate that starts after the uterine contraction has already begun. There is a delay between the uterine contraction and the deceleration. The lowest point of the declaration occurs after the peak of the contraction. Late decelerations are caused by hypoxia in the fetus

299
Q

what are variable decelerations

A

abrupt decelerations that may be unrelated to uterine contractions. There is a fall of more than 15 bpm from the baseline. The lowest point of the declaration occurs within 30 seconds, and the deceleration lasts less than 2 minutes in total. Variable decelerations often indicate intermittent compression of the umbilical cord, causing fetal hypoxia

300
Q

what are prolonged decelerations

A

Prolonged decelerations last between 2 and 10 minutes with a drop of more than 15 bpm from baseline. This often indicates compression of the umbilical cord, causing fetal hypoxia. These are abnormal and concerning.

301
Q

what is fetal scalp stimulation

A

done at times of decelerations, an acceleration in response to stimulation is a reassuring sign

302
Q

what is the rule of 3’s for fetal bradycardia

A

3 minutes – call for help
6 minutes – move to theatre
9 minutes – prepare for delivery
12 minutes – deliver the baby (by 15 minutes)

303
Q

what is a sinusoidal CTG

A

rare pattern to be aware of, as it can indicate severe fetal compromise. It gives a pattern similar to a sine wave, with smooth regular waves up and down that have an amplitude of 5 – 15 bpm. It is usually associated with severe fetal anaemia, for example, caused by vasa praevia with fetal haemorrhage.

304
Q

what is the mnemonic used to assess the features of a CTG in a structured way

A

DR C BRaVADO
DR – Define Risk (define the risk based on the individual woman and pregnancy before assessing the CTG)
C – Contractions
BRa – Baseline Rate
V – Variability
A – Accelerations
D – Decelerations
O – Overall impression (given an overall impression of the CTG and clinical picture)

305
Q

what is oxytocin infusion in labour used for

A

Induce labour
Progress labour
Improve the frequency and strength of uterine contractions
Prevent or treat postpartum haemorrhage

306
Q

when is ergometrine used in labour

A

it is used to stimulate smooth muscle contraction, and may be used during the third stage of labour
- has severe side effects as it acts on smooth muscle in blood vessels and GI tract, should be avoided in eclampsia
- used as syntometrine which is a combination of oxytocin and ergometrine

307
Q

when are prostaglandins used in pregnancy

A

This is used for induction of labour, and can come in one of three forms:
Vaginal pessaries (Propess)
Vaginal tablets (Prostin tablets)
Vaginal gel (Prostin gel)

308
Q

when is nifedipine used in pregnancy

A

Calcium channel blocker
It has two main uses in pregnancy:
Reduce blood pressure in hypertension and pre-eclampsia
Tocolysis in premature labour, where it suppresses uterine activity and delays the onset of labour

309
Q

when is terbutaline used in pregnancy

A

Beta 2 agonist
It is used for tocolysis in uterine hyperstimulation, notably when the uterine contractions become excessive during induction of labour.
also used to perform ECV

310
Q

when is carboprost used in labour

A

Carboprost is a synthetic prostaglandin analogue, meaning it binds to prostaglandin receptors. It stimulates uterine contraction. It is given as a deep intramuscular injection in postpartum haemorrhage, where ergometrine and oxytocin have been inadequate
- avoid in asthma patients

311
Q

when is tranexamic acid used in patients

A

Tranexamic acid is used in the prevention and treatment of postpartum haemorrhage.
- antifibrinolytic medication

312
Q

when is delay in the first stage of labour considered

A

when there is either:
Less than 2cm of cervical dilatation in 4 hours
Slowing of progress in a multiparous women

313
Q

what is a partogram and what does it measure

A

used for monitoring a womans progress in the first stage of labour, monitors:
cervical dilation
descent of fetal head
maternal pulse, BP, temp and urine output
fetal heart rate
contraction frequency
status of membranes, presence of liquor and whether its stained with blood/meconium
drugs and fluids which have been given

314
Q

when is delay in the second stage of labour considered

A

when the active second stage (pushing) lasts over:
2 hours in a nulliparous woman
1 hour in a multiparous woman

315
Q

what are the different lies a baby can be in

A

Longitudinal lie – the fetus is straight up and down
Transverse lie – the fetus is straight side to side
Oblique lie – the fetus is at an angle

316
Q

what is delay of the third stage of labour defined as

A

More than 30 minutes with active management
More than 60 minutes with physiological management

317
Q

what pain medication is used in pregnancy

A
  1. Simple analgesia: paracetamol
  2. Gas and Air (Entonox)
  3. IM Pethidine or Diamorphine (opioid injections)
  4. Patient controlled analgesia - remifentanil
  5. Epidural - into the epidural space outside the dura mater. options are levobupivacaine or bupivacaine mixed with fentanyl
318
Q

what are adverse effects of an epidural

A

Headache after insertion
Hypotension
Motor weakness in the legs
Nerve damage
Prolonged second stage
Increased probability of instrumental delivery

319
Q

what is umbilical cord prolapse

A

this is when the umbilical cord descends below the presenting part of the fetus and through the cervix into the vagina after ROM

320
Q

what is the most significant risk factors for umbilical cord prolapse

A

when the fetus is in an abnormal lie after 37 weeks gestation (i.e. unstable, transverse or oblique)

321
Q

what is the management of umbilical cord prolapse

A

emergency caesarean section
- when the baby is compressing a prolapsed cord the presenting part can be pushed up to prevent compression
- women can lie in left lateral position or knee chest position
- tocolytic medication can be used to minimise contractions while wating for caesarean

322
Q

what are the risks of instrumental delivery

A

key risks to mum are
Postpartum haemorrhage
Episiotomy
Perineal tears
Injury to the anal sphincter
Incontinence of the bladder or bowel
Nerve injury (obturator or femoral nerve)

The key risks to remember to the baby are:
Cephalohaematoma with ventouse
Facial nerve palsy with forceps
subgaleal haemorrhage
intracranial haemorrhage
skull fracture
spinal cord injury

323
Q

what is the main complication of a ventouse delivery for baby

A

cephalohaematoma

324
Q

what is the main complication of forceps delivery for baby

A

facial nerve palsy

325
Q

what are indications for instrumental delivery

A

Failure to progress
Fetal distress
Maternal exhaustion
Control of the head in various fetal positions

326
Q

what nerve injury can occur in the mother during instrumental delivery

A

The affected nerves may be:
Femoral nerve
Obturator nerve

327
Q

what nerve injuries can occur during birth that are unrelated to instrumental delivery

A

Lateral cutaneous nerve of the thigh
Lumbosacral plexus
Common peroneal nerve

328
Q

what circumstances are perineal tears common

A

First births (nulliparity)
Large babies (over 4kg)
Shoulder dystocia
Asian ethnicity
Occipito-posterior position
Instrumental deliveries

329
Q

what is the classification of perineal tears

A

First-degree – injury limited to the frenulum of the labia minora (where they meet posteriorly) and superficial skin
Second-degree – including the perineal muscles, but not affecting the anal sphincter
Third-degree – including the anal sphincter, but not affecting the rectal mucosa
Fourth-degree – including the rectal mucosa

330
Q

what are the third degree subcategories for perineal tears

A

3A – less than 50% of the external anal sphincter affected
3B – more than 50% of the external anal sphincter affected
3C – external and internal anal sphincter affected

331
Q

what is the management of perineal tears

A

first degree usually done require sutures
anything larger than first degree usually requires sutures
third or fourth degree is likely to require repairing in theatre
to prevent complications: broad spectrum Abx, laxatives, physio, follow up

332
Q

what are short term complications after perineal tear repair

A

Pain
Infection
Bleeding
Wound dehiscence or wound breakdown

333
Q

what are lasting complications that can come from perineal tears

A

Urinary incontinence
Anal incontinence and altered bowel habit (third and fourth-degree tears)
Fistula between the vagina and bowel (rare)
Sexual dysfunction and dyspareunia (painful sex)
Psychological and mental health consequences

334
Q

what is perineal massage

A

Perineal massage is a method for reducing the risk of perineal tears. It involves massaging the skin and tissues between the vagina and anus (perineum). This is done in a structured way from 34 weeks onwards to stretch and prepare the tissues for delivery.

335
Q

what are the two classifications of post partum haemorrhage

A

Minor PPH – under 1000ml blood loss
Major PPH – over 1000ml blood loss
OR
Primary PPH: bleeding within 24 hours of birth
Secondary PPH: from 24 hours to 12 weeks after birth

336
Q

what are the two sub-classifications of major PPH

A

Moderate PPH – 1000 – 2000ml blood loss
Severe PPH – over 2000ml blood loss

337
Q

what is the management if someone has a post partum haemorrhage

A

Resuscitation with an ABCDE approach
Lie the woman flat, keep her warm and communicate with her and the partner
Insert two large-bore cannulas
Bloods for FBC, U&E and clotting screen
Group and cross match 4 units
Warmed IV fluid and blood resuscitation as required
Oxygen (regardless of saturations)
Fresh frozen plasma is used where there are clotting abnormalities or after 4 units of blood transfusion

338
Q

what are the mechanical treatment options for stopping bleeding in PPH

A

Rubbing the uterus through the abdomen to stimulates a uterine contraction (referred to as “rubbing up the fundus”)
Catheterisation (bladder distention prevents uterus contractions)

339
Q

what are the medical treatments to stop bleeding in a PPH

A

Oxytocin (slow injection followed by continuous infusion)
Ergometrine (intravenous or intramuscular) stimulates smooth muscle contraction (contraindicated in hypertension)
Carboprost (intramuscular) is a prostaglandin analogue and stimulates uterine contraction (caution in asthma)
Misoprostol (sublingual) is also a prostaglandin analogue and stimulates uterine contraction
Tranexamic acid (intravenous) is an antifibrinolytic that reduces bleeding

340
Q

what are the surgical treatments to stopping bleeding in a PPH

A

Intrauterine balloon tamponade – inserting an inflatable balloon into the uterus to press against the bleeding
B-Lynch suture – putting a suture around the uterus to compress it
Uterine artery ligation – ligation of one or more of the arteries supplying the uterus to reduce the blood flow
Hysterectomy is the “last resort” but will stop the bleeding and may save the woman’s life

341
Q

what are risk factors for PPH

A

Previous PPH
Multiple pregnancy
Obesity
Large baby
Failure to progress in the second stage of labour
Prolonged third stage
Pre-eclampsia
Placenta accreta
Retained placenta
Instrumental delivery
General anaesthesia
Episiotomy or perineal tear

342
Q

what are indications for elective caesarean

A

Previous caesarean
Symptomatic after a previous significant perineal tear
Placenta praevia
Vasa praevia
Breech presentation
Multiple pregnancy
Uncontrolled HIV infection
Cervical cancer

343
Q

what are the 4 types of emergency caesarean

A

Category 1: There is an immediate threat to the life of the mother or baby. Decision to delivery time is 30 minutes.
Category 2: There is not an imminent threat to life, but caesarean is required urgently due to compromise of the mother or baby. Decision to delivery time is 75 minutes.
Category 3: Delivery is required, but mother and baby are stable.
Category 4: This is an elective caesarean, as described above.

344
Q

what are the layers of the abdomen that need to be dissected through in a caesarean

A

Skin
Subcutaneous tissue
Fascia / rectus sheath (the aponeurosis of the transversus abdominis and external and internal oblique muscles)
Rectus abdominis muscles (separated vertically)
Peritoneum
Vesicouterine peritoneum (and bladder) – the bladder is separated from the uterus with a bladder flap
Uterus (perimetrium, myometrium and endometrium)
Amniotic sac

345
Q

what are the two kinds of incision used in a caesarean section

A

Pfannenstiel incision is a curved incision two fingers width above the pubic symphysis
Joel-cohen incision is a straight incision that is slightly higher (this is the recommended incision)

346
Q

what measures can be done to reduce risks during a caesarean section

A

H2 receptor antagonists (e.g. ranitidine) or proton pump inhibitors (e.g. omeprazole) before the procedure
Prophylactic antibiotics during the procedure to reduce the risk of infection
Oxytocin during the procedure to reduce the risk of postpartum haemorrhage
Venous thromboembolism (VTE) prophylaxis with low molecular weight heparin

347
Q

can a woman give birth vaginally after a caesarean

A

it is possible provided the cause of the caesarean is unlikely to reoccur
- contraindications is previous uterine rupture, classical caesarean scare (vertical) or usual contraindications to vaginal delivery

348
Q

what are the two key causes of sepsis in pregnancy

A

Chorioamnionitis
Urinary tract infections

349
Q

what are non specific signs of sepsis

A

Fever
Tachycardia
Raised respiratory rate (often an early sign)
Reduced oxygen saturations
Low blood pressure
Altered consciousness
Reduced urine output
Raised white blood cells on a full blood count
Evidence of fetal compromise on a CTG

350
Q

what chart is used to monitor women and their chance of sepsis

A

maternity early obstetric warning system (MEOWS)

351
Q

what are signs of chorioamnionitis

A

Abdominal pain
Uterine tenderness
Vaginal discharge

352
Q

what is the management of sepsis in pregnancy

A

Septic six - take blood, lactate and urine output, give abx, fluids and oxygen
continuous maternal and fetal monitoring
emergency caesarean may be indicated
antibiotics - piperacillin and tazobactam plus gentamicin/ amoxicillin clindamycin and gentamicin

353
Q

what is amniotic fluid embolism

A

it is where amniotic fluid passes into the mothers blood - usually occurs around labour and delivery
the amniotic fluid contains fetal tissue which causes an immune reaction. This leads to systemic illness

354
Q

what are the main risk factors for amniotic fluid embolism

A

Increasing maternal age
Induction of labour
Caesarean section
Multiple pregnancy

355
Q

how does amniotic fluid embolism present

A

can present similar to anaphylaxis, sepsis or PE
Shortness of breath
Hypoxia
Hypotension
Coagulopathy
Haemorrhage
Tachycardia
Confusion
Seizures
Cardiac arrest

356
Q

what is the management of amniotic fluid embolism

A

supportive
medical emergency - ABCDE
resuscitation and immediate caesarean if there is cardiac arrest

357
Q

what is uterine rupture

A

when the muscle layer of the uterus ruptures
- incomplete - uterine serosa surrounding the uterus retains intact
- complete - serosa ruptures along with the myometrium and the contents of the uterus are released into the peritoneal cavity

358
Q

what are risk factors for uterine rupture

A

previous caesarean section (main RF)
Vaginal birth after caesarean (VBAC)
Previous uterine surgery
Increased BMI
High parity
Increased age
Induction of labour
Use of oxytocin to stimulate contractions

359
Q

how does uterine rupture present

A

Uterine rupture presents with an acutely unwell mother and abnormal CTG. It may occur with induction or augmentation of labour, with signs and symptoms of:
Abdominal pain
Vaginal bleeding
Ceasing of uterine contractions
Hypotension
Tachycardia
Collapse

360
Q

what is the management of uterine rupture

A

Uterine rupture is an obstetric emergency. Resuscitation and transfusion may be required. Emergency caesarean section is necessary to remove the baby, stop any bleeding and repair or remove the uterus (hysterectomy).

361
Q

what is uterine inversion

A

rare complication of birth, where the fundus of the uterus drops down through the uterine cavity and cervix, turning the uterus inside out
- life threatening obstetric emergency
- incomplete is where the fundus descends inside uterus or vagina but not to vaginal opening
- complete is the uterus descending through and out of the vagina

362
Q

how does uterine inversion present

A

Uterine inversion typically presents with a large postpartum haemorrhage. There may be maternal shock or collapse.

An incomplete uterine inversion may be felt with manual vaginal examination. With a complete uterine inversion, the uterus may be seen at the introitus of the vagina.

363
Q

what are the options for treating uterine inversion

A
  1. Johnson manoeuvre - using a hand to push the fundus back into the abdomen. Hand and forearm must be inserted into the vagina and held in place for several minutes
  2. Hydrostatic methods - filling vagina with fluid to inflate the uterus back into the normal position
  3. Surgery - laparotomy and uterus put back into normal position
364
Q

in girls what starts the onset of puberty

A

the development of breast buds

365
Q

what is tanner stage 1 for female puberty

A

under 10
no pubic hair
no breast development

366
Q

what is tanner stage 2 for female puberty

A

age 10 -11
light and thin pubic hair
breast buds form from behind the areola

367
Q

what is tanner stage 3 for female puberty

A

age 11-13
course and curly pubic hair
breast begins to elevate beyond the areola

368
Q

what is tanner stage 4 for female puberty

A

age 13-24
adult like pubic hair but not reaching the thigh
areolar mound forms and projects from surrounding breast

369
Q

what is tanner stage 5 for female puberty

A

above 14 years
pubic hair extending to medial thigh
areolar mounds reduce and adult breasts form

370
Q

how does the primary follicle develop

A

Primordial follicles grow and become primary follicles. These primary follicles have three layers:
The primary oocyte in the centre
The zona pellucida
The cuboidal shaped granulosa cells
the granulosa cells secrete the material that becomes the zona pellucida and oestrogen
as they grow they develop a surrounding theca folliculi layer (inner layer of this is the theca interna which secretes androgen hormones)

371
Q

how does the secondary follicle develop

A

as primary follicles become secondary follicles they grow larger and develop small fluid filled gaps between the granulosa cells. Once the follicle reaches the secondary follicle stage they have FSH receptors and further development requires FSH stimulation

372
Q

how do antral follicles develop

A

the secondary follicle develops a single large fluid filled area within the granulosa cells called the antrum. This fills with increasing amounts of fluid making the follicle expand rapidly
the corona radiata is made of granulosa cells and surrounds the zona pellucida and the oocyte
at this point one follicle becomes the dominant follicle and the others start to degrade

373
Q

what is the process of fertilisation

A

when sperm enter the fallopian tube they will penetrate the corona radiata and zona pellucida to fertilise the egg
when the sperm enters the egg the 23 chromosomes of the egg multiply into two sets, one set combine with the sperm chromosomes and the other float off to the side and create a polar body

374
Q

what is a polar body

A

just before ovulation the primary oocyte undergoes meiosis, splitting the 46 chromosomes in the oocyte into two leaving 23, the other 23 float off and become a polar body

375
Q

how does the blastocyst develop

A

the combination of the egg and sperm produces a zygote
this rapidly divides to create a mass of cells called a morula
as it travels along the fallopian tube a fluid filled cavity gathers within the group of cells and it becomes a blastocyst
the blastocyst contains the main group of cells in the middle (embryoblast), and surrounding the embryoblast and blastocele is the trophoblast

376
Q

how does implantation occur

A

when the blastocyst arrives at the uterus 8-10 days after ovulation it reaches the endometrium
the cells of the trophoblast undergo adhesion to the stroma of the endometrium, forming the syncytiotrophoblast which forms projections into the stoma
the cells of the stoma become decidua which provides nutrients to the trophoblast
when it implants the syncytiotrophoblast starts to produce bHCG

377
Q

when do the cells of the embryoblast start to differentiate

A

about a week after fertilisation - splits into two with the yolk sac on one side and the amniotic cavity on the other
the embryonic disc develops into the fetal pole and eventually into the fetus

378
Q

what are the two layers of the chorion

A

the cytotrophoblast and the syncytiotrophoblast. The cytotrophoblast is the inner layer and the syncytiotrophoblast is the outer layer, which is embedded in the endometrium.

379
Q

what week does the embryonic disc develop into the fetal pole

A

week 5 - splits into the ectoderm, mesoderm, endoderm

380
Q

what does the endoderm become in the body

A

GIT
lungs
liver
pancreas
thyroid
reproductive system

381
Q

what does the mesoderm become

A

heart
muscle
bone
connective tissue
blood
kidneys

382
Q

what does the ectoderm become

A

skin
hair
nails
teeth
CNS

383
Q

when does the fetal heart form

A

week 6

384
Q

how do spiral arteries develop

A

The myometrium sends off artery branches into the endometrium. Initially, these arteries grow straight outwards like plant shoots. As they continue to grow, they coil into a spiral. These thick-walled and coiled arteries are bunched together, making the endometrial tissue highly vascular. These are known as the spiral arteries.

385
Q

how does the placenta develop

A

The chorionic villi (syncytiotrophoblast that grows into endometrium) nearest the connecting stalk of the developing embryo are the most vascular and contain mesoderm. This area is called the chorion frondosum. The cells in the chorion frondosum proliferate and become the placenta. The connecting stalk becomes the umbilical cord. Placental development is usually complete by 10 weeks gestation.

386
Q

how do the lacunae develop

A

Trophoblast invasion of the endometrium sends signals to the spiral arteries in that area, reducing their vascular resistance and making them more fragile. The blood flow to these arteries increases, and eventually they break down, leaving pools of blood called lacunae (lakes). Maternal blood flows from the uterine arteries, into these lacunae, and back out through the uterine veins. Lacunae form at around 20 weeks gestation.

387
Q

what are the 5 functions of the placenta

A

Respiratory
Renal/excretion
Nutrition
immunity
endocrine

388
Q

what immunoglobulin crosses the placenta

A

IgG

389
Q

what waste products are filtered from the fetus via the placenta

A

urea and creatinine

390
Q

what endocrine functions does the placenta have

A

production of hCG around week 10
oestrogen - allows muscles and ligaments of uterus and pelvis to expand, cervix soft
progesterone - placenta takes over by 5 weeks, role is to maintain pregnancy and relaxes uterine muscles (SA= reflux, constipation, hypotension, headaches, skin flushing)

391
Q

what are the hormonal changes during pregnancy

A

increased steroid hormones
increased T3/T4
increased prolactin
increased melanocyte stimulating hormone
increased oestrogen
increased progesterone
increased HCG

392
Q

what are the respiratory changes in pregnancy

A

increased tidal volume
increased resp. rate

393
Q

what are the renal changes in pregnancy

A

increased blood flow
increased GFR
increased sodium reabsorption
increased water reabsorption
increased protein excretion
physiological hydronephrosis

394
Q

what are the haematological changes in pregnancy

A

increased red blood cell production
increased white blood cells
reduced platelets
decreased haematocrit
increased clotting factors
decreased albumin
increased ALP (placenta)

395
Q

what are the cardiovascular changes in pregnancy

A

increased blood volume
increased plasma volume
increased cardiac output
decreased vascular resistance
decreased blood pressure
vasodilation
varicose veins

396
Q

what are the uterine changes in pregnancy

A

100g - 1.1kg
hypertrophy
increased cervical discharge
ectropion
vagina hypertrophy, increased discharge, candida, bacteria

397
Q

what are Braxton hicks contractions

A

Braxton-Hicks contractions are occasional irregular contractions of the uterus. They are usually felt during the second and third trimester. Women can experience temporary and irregular tightening or mild cramping in the abdomen

398
Q
A