Sexual health Flashcards

Conditions and Presentations

1
Q

Syphilis

A

sexually transmitted infection caused by the spirochaete Treponema pallidum.

Infection is characterised by primary, secondary and tertiary stages.
The incubation period is between 9-90 days

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2
Q

Primary features Syphilis

A

chancre - painless ulcer at the site of sexual contact
local non-tender lymphadenopathy
often not seen in women (the lesion may be on the cervix)

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3
Q

secondary features Syphilis

A
  • occurs 6-10 weeks after primary infection
    systemic symptoms: fevers, lymphadenopathy
    rash on trunk, palms and soles
    buccal ‘snail track’ ulcers (30%)
    condylomata lata (painless, warty lesions on the genitalia )
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4
Q

Tertiary features of Syphilis

A

gummas (granulomatous lesions of the skin and bones)
ascending aortic aneurysms
general paralysis of the insane
tabes dorsalis
Argyll-Robertson pupil

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5
Q

Features of congenital syphilis

A
  • blunted upper incisor teeth (Hutchinson’s teeth), ‘mulberry’ molars
  • rhagades (linear scars at the angle of the mouth)
  • keratitis
  • saber shins
  • saddle nose
  • deafness
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6
Q

Investigations of syphilis

A

Treponema pallidum is a very sensitive organism and cannot be grown on artificial media.
The diagnosis is therefore usually based on clinical features, serology and microscopic examination of infected tissue.

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7
Q

Non-treponemal tests

A
  • not specific for syphilis, therefore may result in false positives
  • based upon the reactivity of serum from infected patients to a cardiolipin-cholesterol-lecithin antigen
  • assesses the quantity of antibodies being produced
  • becomes negative after treatment
  • examples include: rapid plasma reagin (RPR) and Venereal Disease Research Laboratory (VDRL)
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8
Q

treponemal-specific tests

A

generally more complex and expensive but specific for syphilis
qualitative only and are reported as ‘reactive’ or ‘non-reactive’
examples include: TP-EIA (T. pallidum enzyme immunoassay), TPHA (T. pallidum HaemAgglutination test)
the TP-EIA test has become increasingly popular in recent years

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9
Q

Reasons for false positives on non-treponemal tests

A

pregnancy
SLE, anti-phospholipid syndrome
tuberculosis
leprosy
malaria
HIV

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10
Q

Interpretating test results for syphilis

A

Positive non-treponemal test + positive treponemal test
consistent with active syphilis infection

Positive non-treponemal test + negative treponemal test
consistent with a false-positive syphilis result e.g. due to pregnancy or SLE (see list above)

Negative non-treponemal test + positive treponemal test :
consistent with successfully treated syphilis

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11
Q

Managment of syphilis

A

intramuscular benzathine penicillin is the first-line management

alternatives: doxycycline

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12
Q

Jarisch-Herxheimer reaction

A

fever, rash, tachycardia after the first dose of antibiotic
in contrast to anaphylaxis, there is no wheeze or hypotension
it is thought to be due to the release of endotoxins following bacterial death and typically occurs within a few hours of treatment
no treatment is needed other than antipyretics if required

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13
Q

Gonorrhea

A

Gonorrhea is a sexually transmitted infection (STI) caused by the bacterium Neisseria gonorrhoeae. It primarily affects the mucous membranes of the genital tract, but it can also infect the rectum, throat, and eyes

gram positive diplococci

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14
Q

Transmission of gonorrhea

A

Gonorrhea is spread through sexual contact with an infected person, including vaginal, anal, or oral sex. It can also be transmitted from mother to baby during childbirth.

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15
Q

Male symptoms of gonnorhea

A

Urethral discharge (pus-like or milky discharge from the penis)
Pain or burning sensation during urination
Testicular pain or swelling

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16
Q

Female symtpoms of gonorrhea

A

Vaginal discharge (often greenish or yellowish)
Pain or burning sensation during urination
Pelvic pain
Abnormal vaginal bleeding
asymptomatic causes

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17
Q

complications of gonorrhea

A

Pelvic inflammatory disease (PID) in women, leading to infertility or ectopic pregnancy
Epididymitis (inflammation of the epididymis) in men, leading to infertility
Disseminated gonococcal infection (DGI), causing joint pain, skin rash, and fever
Increased risk of HIV transmission
Conjunctivitis (eye infection) in newborns born to infected mothers

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18
Q

Diagnosis of gonorrhea

A

Nucleic acid amplification tests (NAATs) on urine, vaginal, cervical, rectal, or throat swabs
Gram stain or culture of urethral, cervical, or rectal specimens
Examination of discharge or lesions under a microscope

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19
Q

Treatment of gonorrhea

A

Antibiotic therapy with dual therapy (typically ceftriaxone plus azithromycin) to reduce the risk of antibiotic resistance
Treatment of sexual partners to prevent reinfection and further transmission
Follow-up testing to ensure successful treatment and to detect reinfection

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20
Q

Prevention of gonorrhea

A

Abstinence or mutual monogamy with an uninfected partner
Correct and consistent use of condoms during sexual activity
Routine screening for gonorrhea and other STIs, especially in high-risk populations
Vaccination (if available in the future)

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21
Q

Prognosis of Gonorrhea

A

Gonorrhea is curable with appropriate antibiotic treatment, but reinfection is common without behavioral changes or partner treatment.
Early detection and treatment are essential to prevent complications and reduce the risk of transmission.

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22
Q

Chlamydia

A

most prevalent sexually transmitted infection in the UK and is caused by Chlamydia trachomatis, an obligate intracellular pathogen

1 in 10 young women in the UK have Chlamydia. The incubation period is around 7-21 days, although it should be remembered a large percentage of cases are asymptomatic

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23
Q

Features of Chlamydia

A

asymptomatic in around 70% of women and 50% of men
women: cervicitis (discharge, bleeding), dysuria
men: urethral discharge, dysuria

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24
Q

complications of Chlamydia

A

epididymitis
pelvic inflammatory disease
endometritis
increased incidence of ectopic pregnancies
infertility
reactive arthritis
perihepatitis (Fitz-Hugh-Curtis syndrome)

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25
Q

Investigations of Chlamydia

A

traditional cell culture is no longer widely used
nuclear acid amplification tests (NAATs) are now the investigation of choice
urine (first void urine sample), vulvovaginal swab or cervical swab may be tested using the NAAT technique
for women: the vulvovaginal swab is first-line
for men: the urine test is first-line
Chlamydiatesting should be carried out two weeks after a possible exposure

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26
Q

Screening of Chalmydia

A

in England the National Chlamydia Screening Programme is open to all men and women aged 15-24 years
the 2009 SIGN guidelines support this approach, suggesting screening all sexually active patients aged 15-24 years
relies heavily on opportunistic testing

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27
Q

Managment of Chlamydia

A

-doxycycline (7 day course) if first-line

-if doxycycline is contraindicated / not tolerated then either azithromycin (1g od for one day, then 500mg od for two days) should be used

if pregnant then azithromycin, erythromycin or amoxicillin may be used.

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28
Q

contact tracing chlamidya

A

offered a choice of provider for initial partner notification - either trained practice nurses with support from GUM, or referral to GUM

for men with urethral symptoms: all contacts since, and in the four weeks prior to, the onset of symptoms
for women and asymptomatic men all partners from the last six months or the most recent sexual partner should be contacted
contacts of confirmed Chlamydia cases should be offered treatment prior to the results of their investigations being known (treat then test

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29
Q

risk factors for ED

A
  • ageing
    -cardiovascular disease
    -risk factors: obesity, diabetes mellitus, dyslipidaemia, metabolic syndrome, hypertension, -smoking
    -alcohol use
    -drugs: SSRIs, beta-blockers
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30
Q

treatment of ED

A

PDE-5 inhibitors (such as sildenafil, ‘Viagra’) have revolutionised the management of ED
they should be prescribed (in the absence of contraindications) to all patients regardless of aetiology
sildenafil can be purchased over-the-counter without a prescription.

-Vacuum erection devices are recommended as first-line treatment in those who can’t/won’t take a PDE-5 inhibitor.

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31
Q

ED referrals and exercise

A

for a young man who has always had difficulty achieving an erection, referral to urology is appropriate
people with erectile dysfunction who cycle for more than three hours per week should be advised to stop

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32
Q

sildenafil (Viagra)

A

this was the first phosphodiesterase type V inhibitor
short-acting - usually taken 1 hour before sexual activity

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33
Q

tadalafil (Cialis)

A

longer acting than sildenafil, may be taken on a regular basis (e.g. once daily)

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34
Q

contradictions to taking Phosphodiesterase type V inhibitors

A

patients taking nitrates and related drugs such as nicorandil
hypotension
recent stroke or myocardial infarction (NICE recommend waiting 6 months)

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35
Q

side effects of Phosphodiesterase type V inhibitors

A

visual disturbances
blue discolouration
non-arteritic anterior ischaemic neuropathy
nasal congestion
flushing
gastrointestinal side-effects
headache
priapism

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36
Q

Atrophic vaginitis

A

-Atrophic vaginitis often occurs in women who are post-menopausal women.

  • It presents with vaginal dryness, dyspareunia and occasional spotting.

-On examination, the vagina may appear pale and dry.

-Treatment is with vaginal lubricants and moisturisers - if these do not help then topical oestrogen cream can be used.

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37
Q

Pelvic inflammatory disease

A

Pelvic inflammatory disease (PID) is a term used to describe infection and inflammation of the female pelvic organs including the uterus, fallopian tubes, ovaries and the surrounding peritoneum. It is usually the result of ascending infection from the endocervix.

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38
Q

causative agents of PID

A

Chlamydia trachomatis
+ the most common cause
Neisseria gonorrhoeae
Mycoplasma genitalium
Mycoplasma hominis

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39
Q

Features of PID

A

lower abdominal pain
fever
deep dyspareunia
dysuria and menstrual irregularities may occur
vaginal or cervical discharge
cervical excitation

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40
Q

Investigations for PID

A

a pregnancy test should be done to exclude an ectopic pregnancy
high vaginal swab
these are often negative
screen for Chlamydia and Gonorrhoea

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41
Q

Managment of PID

A

oral ofloxacin + oral metronidazole or intramuscular ceftriaxone + oral doxycycline + oral metronidazole

Removal of the IUD should be considered and may be associated with better short term clinical outcomes’

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42
Q

Complications of PID

A

perihepatitis (Fitz-Hugh Curtis Syndrome)
occurs in around 10% of cases
it is characterised by right upper quadrant pain and may be confused with cholecystitis
infertility - the risk may be as high as 10-20% after a single episode
chronic pelvic pain
ectopic pregnancy

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43
Q

Fitz-Hugh Curtis Syndrome

A

Inflammation of the liver capsule, without the involvement of the liver parenchyma, with adhesion formation accompanied by right upper quadrant pain.

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44
Q

Thrush/ candidasis

A

Vaginal candidiasis (‘thrush’) is an extremely common condition which many women diagnose and treat themselves

common cause is Candida albicans

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45
Q

predispositioning factors to thrush

A

diabetes mellitus
drugs: antibiotics, steroids
pregnancy
immunosuppression: HIV

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46
Q

Signs and symptoms of Thrush

A

‘cottage cheese’, non-offensive discharge
vulvitis: superficial dyspareunia, dysuria
itch
vulval erythema, fissuring, satellite lesions may be seen

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47
Q

Investigations of thrush

A

a high vaginal swab is not routinely indicated if the clinical features are consistent with candidiasis

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48
Q

Managment of thrush

A

options include local or oral treatment
NICE Clinical Knowledge Summaries recommends:
oral fluconazole 150 mg as a single dose first-line
clotrimazole 500 mg intravaginal pessary as a single dose if oral therapy is contraindicated
If there are vulval symptoms, consider adding a topical imidazole in addition to an oral or intravaginal antifungal
if pregnant then only local treatments (e.g. cream or pessaries) may be used - oral treatments are contraindicated

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49
Q

Recurrent thrush managment

A
  • BASHH define recurrent vaginal candidiasis as 4 or more episodes per year

-compliance with previous treatment should be checked

-confirm the diagnosis of candidiasis
-high vaginal swab for microscopy and culture
consider a blood glucose test to exclude diabetes

exclude differential diagnoses such as lichen sclerosus
consider the use of an induction-maintenance regime
induction: oral fluconazole every 3 days for 3 doses
maintenance: oral fluconazole weekly for 6 months

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50
Q

what is the definitive treatment of Bartholin’s abcess called?

A

-marsupialization.

  • Insertion of a catheter to treat the abcess with antibioitics
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51
Q

Bartholins abcess

A

Bartholin’s abscess is a painful swelling or lump that forms when the Bartholin’s gland becomes blocked, causing fluid buildup and infection.

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52
Q

Symptoms of Bartholin’s abcess

A

Pain and tenderness in the vaginal area
Swelling or lump near the vaginal opening
Discomfort or pain during sexual intercourse
Difficulty walking or sitting
Fever and chills (if infection is present)
Pain with urination or bowel movements (if the abscess is large)

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53
Q

Causes of Bartholin’s abcess

A

Blockage of the ducts of the Bartholin’s glands, often due to infection or inflammation
Bacterial infection, usually by bacteria such as Escherichia coli (E. coli), Streptococcus, or Staphylococcus aureus

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54
Q

Treatment of Bartholin’s abcess

A

Warm compresses or sitz baths to relieve pain and promote drainage
Incision and drainage (I&D) of the abscess to remove pus and relieve pressure
Antibiotics to treat bacterial infection, if present
Marsupialization (surgical procedure to create a permanent opening) for recurrent or large abscesses
Bartholin’s gland excision in severe or recurrent cases

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55
Q

Prevention of Bartholin’s abcess

A

Good genital hygiene
Avoidance of vaginal irritants (such as harsh soaps or douches)
Safe sexual practices (including condom use)
Prompt treatment of genital infections

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56
Q

Bartholin’s cyst

A

-Bartholin’s cyst develops when the entrance to the Bartholin duct becomes blocked.

-The gland continues to produce mucus which builds up behind the blockage, eventually leading to the formation of a mass.

-The initial blockage is most commonly caused by vulvar oedema. These are usually sterile.

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57
Q

Symptoms of Bartholin’s cyst

A

Small painless lump or swelling near the vaginal opening
Discomfort or pressure in the vaginal area
Difficulty walking or sitting if the cyst is large
Discharge from the cyst (if it becomes infected)

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58
Q

Treatment

A

-Warm compresses or sitz baths to promote drainage and relieve discomfort
-Surgical drainage (incision and drainage) for symptomatic or recurrent cysts
-Marsupialization (surgical procedure to create a permanent opening) for recurrent or large cysts
-Antibiotics to treat infection, if present

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59
Q

Vulval carcinoma

A

Vulval carcinoma is a type of cancer that develops in the tissues of the vulva, which is the external part of the female genitalia.

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60
Q

types of vulval cancers

A

Squamous cell carcinoma: The most common type, accounting for the majority of vulvar cancers.
Melanoma: A less common but more aggressive type that arises from melanocytes in the skin of the vulva.
Adenocarcinoma: Arises from the glandular cells in the vulva.

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61
Q

Risk factors of vulvar cancer

A

Age (risk increases with age, most common in women over 60)
Human papillomavirus (HPV) infection
Smoking
Chronic vulvar inflammation or irritation (such as lichen sclerosus)
Immunodeficiency
Previous history of cervical, vaginal, or anal cancer
History of vulvar intraepithelial neoplasia (VIN)

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62
Q

Symptoms of vulvar cancer

A

Persistent itching, pain, or tenderness in the vulvar area
Lump, mass, or ulcer on the vulva that doesn’t heal
Changes in the color or texture of the skin of the vulva
Bleeding or discharge not related to menstruation
Burning or pain during urination

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63
Q

Diagnosis of vulvar cancer

A

Physical examination of the vulva, including visual inspection and palpation
Biopsy of suspicious lesions for pathological examination
Imaging tests (such as ultrasound, CT scan, or MRI) to assess the extent of the cancer and identify metastasis

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64
Q

Preventative measures of vulvar cancer

A

HPV vaccination (for prevention of HPV-related vulvar cancers)
Avoidance of smoking
Regular gynecological examinations and screening tests (Pap smear, HPV testing)

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65
Q

risk factors for vulvar cancer

A

Human papilloma virus (HPV) infection
Vulval intraepithelial neoplasia (VIN)
Immunosuppression
Lichen sclerosus

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66
Q

Features of vulvar cancer

A

lump or ulcer on the labia majora
inguinal lymphadenopathy
may be associated with itching, irritation

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67
Q

features of genital herpes

A

painful genital ulceration
may be associated with dysuria and pruritus
the primary infection is often more severe than recurrent episodes
systemic features such as headache, fever and malaise are more common in primary episodes
tender inguinal lymphadenopathy
urinary retention may occur

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68
Q

Genital herpes investigation

A

nucleic acid amplification tests (NAAT) is the investigation of choice in genital herpes and are now considered superior to viral culture
HSV serology may be useful in certain situations such as recurrent genital ulceration of unknown cause

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69
Q

Managment of genital herpes

A

general measures include:
saline bathing
analgesia
topical anaesthetic agents e.g. lidocaine
oral aciclovir
some patients with frequent exacerbations may benefit from longer-term aciclovir

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70
Q

Pregnancy and genital herpes

A

elective caesarean section at term is advised if a primary attack of herpes occurs during pregnancy at greater than 28 weeks gestation
women with recurrent herpes who are pregnant should be treated with suppressive therapy and be advised that the risk of transmission to their baby is low

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71
Q

Causes of genital herpes

A

There are two strains of the herpes simplex virus (HSV) in humans: HSV-1 and HSV-2.

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72
Q

Transmission of genital herpes

A

Direct skin-to-skin contact with an infected person during vaginal, anal, or oral sex
Transmission can occur even if the infected person does not have visible sores or symptoms (asymptomatic shedding)
Vertical transmission from mother to baby during childbirth (can lead to neonatal herpes, a potentially serious condition)

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73
Q

Lichen Sclerosus

A

Lichen sclerosus is a chronic inflammatory skin condition characterized by thin, white patches of skin that may appear shiny, smooth, or wrinkled.

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74
Q

Symptoms of Lichen Sclerosus

A

Itching (pruritus) in the affected area, often severe
Pain or discomfort, especially during sexual intercourse or urination
Thinning and tightening of the skin (atrophy), leading to a paper-like appearance
White, patchy lesions that may spread and coalesce
Bleeding, blistering, or ulceration of the affected skin
Scarring and changes in the appearance of the genital or anal area

75
Q

Location of Lichen Scelrosus

A

Genital area: Commonly affects the vulva (in women) and the foreskin or glans penis (in men)
Anal area: Can affect the perianal region, causing itching, discomfort, and pain

76
Q

Risk factors for Lichen Sclerosus

A

Age: Most commonly diagnosed in postmenopausal women, but can occur at any age
Autoimmune diseases (such as thyroid disorders)
Genetic predisposition
Hormonal imbalances
Trauma or irritation to the skin

77
Q

Diagnosis of Lichen sclerosus

A

Clinical examination of the affected skin by a healthcare provider
Skin biopsy to confirm the diagnosis and rule out other conditions

78
Q

Treatment of Lichen Sclerosus

A

Topical corticosteroids: First-line treatment to reduce inflammation, itching, and discomfort (e.g., clobetasol propionate)
Emollients or moisturizers: Used to keep the skin hydrated and reduce dryness and cracking
Immunosuppressive agents (such as tacrolimus or pimecrolimus) for cases resistant to corticosteroids
Phototherapy (narrow-band ultraviolet B therapy) in refractory cases
Regular follow-up and monitoring for early detection of complications (e.g., squamous cell carcinoma)

79
Q

Complications of Lichen Sclerosus

A

Scarring of the genital or anal area
Sexual dysfunction
Phimosis (in men), leading to difficulty retracting the foreskin
Increased risk of squamous cell carcinoma, especially in long-standing or severe cases

80
Q

Prognosis of Lichen Sclerosus

A

Lichen sclerosus is a chronic condition with no cure, but symptoms can often be managed effectively with appropriate treatment.
Regular follow-up with a healthcare provider is important to monitor the condition and prevent complications.

81
Q

Vulval Intraepithelial Neoplasia (VIN)

A

Vulval intraepithelial neoplasia (VIN) refers to precancerous changes in the skin of the vulva, characterized by abnormal growth of cells within the vulvar epithelium.

82
Q

Types of VIN

A

-VIN 1 (mild dysplasia): Minimal abnormal changes in the cells, often considered low-grade or low-risk lesions.

-VIN 2 (moderate dysplasia): Moderate abnormal changes in the cells, indicating a higher risk of progression to vulvar cancer compared to VIN 1.

-VIN 3 (severe dysplasia or carcinoma in situ): Severe abnormal changes in the cells, with a high risk of progression to invasive vulvar cancer if left untreated.

83
Q

Risk factors for VIN

A

-Infection with high-risk types of human papillomavirus (HPV)
-Smoking
-Immunosuppression
-History of vulvar or cervical dysplasia
-Chronic vulvar inflammation or irritation (e.g., lichen sclerosus)

84
Q

Symptoms of VIN

A

-Itching, pain, or burning in the vulvar area
-Redness, thickening, or changes in the color or texture of the vulvar skin
-Presence of lesions or sores on the vulva
-Bleeding or discharge not related to menstruation

85
Q

Diagnosis of VIN

A

-Visual inspection of the vulvar area by a healthcare provider

-Colposcopy: Examination of the vulvar tissue under magnification using a colposcope

-Biopsy: Removal of a small sample of tissue from the abnormal area for pathological examination

86
Q

Treatment of VIN

A

-Observation and monitoring for low-grade lesions (VIN 1)

-Surgical excision or destruction of the abnormal tissue (e.g., laser ablation, electrocautery) for moderate to severe lesions (VIN 2 and VIN 3)

-Topical treatments (e.g., imiquimod cream) for selected cases of VIN

-Regular follow-up and surveillance to monitor for recurrence or progression

87
Q

Prevention of VIN

A

HPV vaccination: Helps prevent infection with high-risk types of HPV, which are associated with VIN and vulvar cancer
Smoking cessation
Safe sexual practices: Condom use may reduce the risk of HPV transmission

88
Q

Prognosis of VIN

A

-Prognosis depends on the grade and extent of -VIN, as well as the effectiveness of treatment.
-Early detection and intervention can prevent progression to invasive vulvar cancer and improve outcomes.

89
Q

Bacterial Vaginosis

A

Bacterial vaginosis is a common vaginal infection caused by an imbalance of bacteria in the vagina, characterized by an overgrowth of harmful bacteria.

90
Q

Etiology of bacterial vaginosis

A

Disruption of the normal balance of vaginal bacteria, particularly a decrease in beneficial lactobacilli and an increase in harmful anaerobic bacteria (such as Gardnerella vaginalis)
Exact cause remains unclear, but factors such as sexual activity, douching, and hormonal changes may contribute to the development of BV

91
Q

Symptoms of BV

A

Thin, white, or gray vaginal discharge with a fishy odor (especially after sexual intercourse or menstruation)
Vaginal itching or irritation
Burning sensation during urination
Discomfort or pain during sexual intercourse

92
Q

Diagnosis of BV

A

Clinical examination of the vaginal discharge and pH testing (pH > 4.5)
Whiff test: Addition of potassium hydroxide (KOH) to vaginal discharge, producing a fishy odor (positive whiff test)
Microscopic examination of vaginal discharge: Presence of clue cells (vaginal epithelial cells covered with bacteria), increased numbers of harmful bacteria, and absence of lactobacilli
Gram stain or culture of vaginal discharge (not routinely performed)

93
Q

Treatment of BV

A

Antibiotic therapy: Oral or vaginal antibiotics (such as metronidazole, clindamycin, or tinidazole) to eliminate the overgrowth of bacteria and restore the normal balance of vaginal flora
Topical treatments (such as vaginal creams or gels) may be used for localized or recurrent BV
Treatment of sexual partners is not routinely recommended unless they have symptoms of BV

94
Q

Complications of BV

A

Increased risk of acquiring sexually transmitted infections (STIs), including HIV
Pelvic inflammatory disease (PID) in severe or recurrent cases
Pregnancy complications (such as preterm birth or low birth weight) in pregnant women with untreated BV

95
Q

Prevention of BV

A

Avoidance of douching and other vaginal irritants
Limiting the number of sexual partners and practicing safer sex (consistent condom use)
Avoiding excessive use of antibiotics, which can disrupt the normal vaginal flora
Regular gynecological examinations and screenings

96
Q

Prognosis of BV

A

Bacterial vaginosis is generally a benign condition but may recur after treatment, particularly in women with certain risk factors.
Prompt diagnosis and appropriate treatment can alleviate symptoms and reduce the risk of complications.

97
Q

Cervical Ectropion

A

Cervical ectropion is a benign condition characterized by the presence of glandular cells from the cervical canal on the outer surface of the cervix.

98
Q

Etiology of cervical ecrtopion

A

Normal physiological variant, especially common in young women and women of reproductive age
Hormonal changes: Estrogen dominance can contribute to the development of cervical ectropion
Pregnancy: Cervical ectropion is often observed during pregnancy due to hormonal fluctuations

99
Q

Symptoms of cervucal ectropion

A

Typically asymptomatic
Vaginal discharge: Increased discharge, often clear or white in color
Spotting or bleeding: May occur after sexual intercourse or pelvic examination
Mild discomfort or irritation: Occasionally reported by some individuals

100
Q

Diagnosis of cervical ectropion

A

Visual examination of the cervix during pelvic examination
Cervical cytology (Pap smear): May reveal the presence of glandular cells on the ectocervix, which can help differentiate cervical ectropion from other cervical abnormalities
Colposcopy: Magnified examination of the cervix using a colposcope, which may show the characteristic appearance of cervical ectropion

101
Q

Treatment of cervical ectropion

A

Typically not required in asymptomatic cases
Symptomatic management: Addressing symptoms such as discharge or bleeding, if present, with conservative measures (e.g., panty liners, topical estrogen cream)
Hormonal contraception: Some individuals may benefit from hormonal methods of contraception (e.g., combined oral contraceptives), which can help regulate hormonal fluctuations and reduce symptoms
Cauterization or cryotherapy: Rarely indicated for severe or refractory cases

102
Q

Complications of cervical ectropion

A

Generally considered a benign condition with no long-term adverse effects
Rarely, persistent or severe symptoms may necessitate further evaluation to rule out other cervical abnormalities or infections

103
Q

Prognosis of cervical ectropion

A

Cervical ectropion is typically a self-limiting condition that resolves spontaneously over time, especially after menopause when hormonal fluctuations decrease.
Regular gynecological examinations may be recommended to monitor the condition, especially in symptomatic individuals.

104
Q

Trichomonas Vaginalis

A

Trichomonas vaginalis is a protozoan parasite that causes trichomoniasis, a common sexually transmitted infection (STI).

105
Q

Transmission of Trichomonas vaginalis

A

Transmission primarily occurs through sexual contact with an infected individual, including vaginal, anal, or oral sex.
Infection can also occur through non-sexual transmission, such as sharing contaminated objects (e.g., towels, sex toys).

106
Q

Symptoms of trichomonas

A

Vaginal discharge: Often frothy, greenish-yellow, or gray in color, with a foul odor
Genital itching or irritation
Pain or discomfort during sexual intercourse (dyspareunia)
Pain or burning sensation during urination (dysuria)
Some individuals may remain asymptomatic

107
Q

Diagnosis of Trichomonas

A

Microscopic examination of vaginal fluid: Identification of motile trichomonads under a microscope (wet mount)
Nucleic acid amplification tests (NAATs): Highly sensitive and specific tests that detect Trichomonas DNA in vaginal or urine samples
Culture: Growth of Trichomonas organisms in culture medium, although less commonly performed

108
Q

Treatment of Trichomonas

A

Oral antibiotics: Metronidazole or tinidazole are commonly used to treat trichomoniasis and eliminate the parasite.
Treatment of sexual partners: All sexual partners should be treated simultaneously to prevent reinfection.

109
Q

Complications of Trichomonas

A

Increased risk of acquiring or transmitting other sexually transmitted infections (STIs), including HIV
Pelvic inflammatory disease (PID) in women, which can lead to infertility or ectopic pregnancy
Preterm birth or low birth weight in pregnant women with untreated trichomoniasis
Increased risk of cervical neoplasia in women with long-standing trichomoniasis

110
Q

Prevention of Trichomonas

A

Safe sexual practices: Consistent and correct use of condoms during sexual intercourse can reduce the risk of trichomoniasis and other STIs.
Limiting the number of sexual partners
Routine screening for STIs, including trichomoniasis, in sexually active individuals

111
Q

Prognosis of Trichomonas

A

Trichomoniasis is generally curable with appropriate treatment, although reinfection can occur if sexual partners are not treated simultaneously.
Early detection and treatment can help prevent complications and reduce the risk of transmission.

112
Q

Candida discharge

A

Cottage cheese’ discharge
Vulvitis
Itch

113
Q

Trichomonas vaginalis discharge

A

Offensive, yellow/green, frothy discharge
Vulvovaginitis
Strawberry cervix

114
Q

Bacterial vaginosis discharge

A

Offensive, thin, white/grey, ‘fishy’ discharge

115
Q

Alpha-fetoprotein

A

Alpha-fetoprotein is a protein produced primarily by the fetal liver during pregnancy.

116
Q

Function of alpha-fetoprotein

A

Transport of nutrients: AFP binds to various molecules (such as fatty acids and steroids) and transports them across the placenta to the developing fetus.
Regulation of fetal growth: AFP may play a role in regulating the growth and development of fetal tissues during pregnancy.

117
Q

Diagnosing uses of alpha-fetoprotein

A

-Prenatal screening: AFP levels in maternal blood are measured as part of prenatal screening tests, such as the triple or quadruple screen, to assess the risk of certain birth defects, including neural tube defects (such as spina bifida) and chromosomal abnormalities (such as Down syndrome).

-Monitoring fetal health: Elevated or decreased AFP levels in amniotic fluid may indicate certain fetal health conditions, such as neural tube defects or gastrointestinal abnormalities.

-Cancer diagnosis and monitoring: Elevated AFP levels in adults may indicate certain types of cancer, particularly liver cancer (hepatocellular carcinoma) and germ cell tumors (such as testicular cancer or ovarian cancer).

118
Q

Elevated alpha-fetoprotein

A

During pregnancy: May indicate an increased risk of
-neural tube defects,
-abdominal wall defects (such as gastroschisis or omphalocele), or
-chromosomal abnormalities in the fetus.
- mutliple pregnancy

In adults: May indicate liver cancer (hepatocellular carcinoma), germ cell tumors, or other types of cancer.

119
Q

Decreased alpha-fetoprotein

A

Down’s syndrome
Trisomy 18
Maternal diabetes mellitus

120
Q

How to measure alpha-fetoprotein

A

Maternal serum screening: AFP levels are measured in maternal blood as part of prenatal screening tests, such as the triple or quadruple screen, usually between 15 and 20 weeks of pregnancy.

Amniocentesis: AFP levels can be measured in amniotic fluid obtained through amniocentesis, a procedure performed during pregnancy to assess fetal health.

121
Q

how much fluid is removed from amniocentesis

A

20 ml of fluid is removed by transabdominal needle under ultrasound guidance

122
Q

Amniocentesis

A

-erformed between 15-20 weeks (typically at 16 weeks) and the risk of fetal loss quoted by the NHS is 0.5%

-karyotype can take 3 weeks to come back.

123
Q

Chancroid

A

Chancroid is a sexually transmitted infection caused by the bacterium Haemophilus ducreyi, characterized by painful genital ulcers and swollen lymph nodes.

124
Q

Etiology of chancroid

A

Caused by the bacterium Haemophilus ducreyi, a fastidious gram-negative bacillus.
Transmission occurs through sexual contact with an infected individual, including vaginal, anal, or oral sex.

125
Q

Symptoms of Chancroid

A

Painful genital ulcers: Typically develop on the penis in men or on the labia, vulva, or perianal area in women. Ulcers are soft, irregular, and often have a friable base.
Swollen lymph nodes (buboes): Enlarged and tender lymph nodes may develop in the groin area.
Pain or discomfort during urination or sexual intercourse
In some cases, systemic symptoms such as fever and malaise may occur

126
Q

Diagnosis of Chancroid

A

Clinical examination: Evaluation of genital ulcers and associated symptoms.
Laboratory tests:
Gram stain or Giemsa stain of ulcer exudate: Identification of gram-negative bacilli or characteristic “school of fish” appearance.
Culture of ulcer swab: Growth of Haemophilus ducreyi in culture medium, although less commonly performed.
Polymerase chain reaction (PCR) testing: Detection of Haemophilus ducreyi DNA in ulcer swab samples, with higher sensitivity compared to culture.

127
Q

Treatment of Chancroid

A

Antibiotic therapy: Oral antibiotics such as azithromycin, ceftriaxone, or erythromycin are commonly used to treat chancroid and eradicate the bacteria.
Drainage of buboes: Large or painful lymph node swellings (buboes) may require aspiration or surgical drainage to relieve symptoms.
Treatment of sexual partners: All sexual partners should be treated simultaneously to prevent reinfection.

128
Q

complications

A

If left untreated, chancroid can lead to complications such as chronic genital ulcers, scarring, or the formation of genital fistulas.
Increased risk of acquiring or transmitting other sexually transmitted infections (STIs), including HIV.

129
Q

Prevention of Charccoid

A

Safer sex practices: Consistent and correct use of condoms during sexual activity can reduce the risk of chancroid and other STIs.
Limiting the number of sexual partners and avoiding high-risk sexual behaviors.

130
Q

Benefits of the COOP (7)

A
  • highly effective (failure rate < 1 per 100 woman years)
  • doesn’t interfere with sex
  • contraceptive effects reversible upon stopping
  • usually makes periods regular, lighter and less painful
  • reduced risk of ovarian, endometrialand colorectal cancer
  • may protect against pelvic inflammatory disease
  • may reduce ovarian cysts, benign breast disease, acne vulgaris
131
Q

Disadvantages of COOP (6)

A
  • may forget to take
  • not STI protection
  • increased VTW risk
  • increased breast and cervical cancer tisk
  • increased risk of stroke and ischaemic heart disease
  • temporary headaches/ breast tenderness
132
Q

Definition of UKMEC 2

A

advantages generally outweigh the disadvantages

132
Q

Definiton of UKMEC 1

A

a condition for which there is no restriction for the use of the contraceptive method

133
Q

UKMEC 3

A

disadvantages generally outweigh the advantage

134
Q

UKMEC 4 defintion

A

represents an unacceptable health risk

135
Q

examples of UKMEC 3 (7)

A
  • more than 35 years old and smoking less than 15 cigarettes/day
  • BMI > 35 kg/m^2*
  • family history of thromboembolic disease in first degree relatives < 45 years
  • controlled hypertension
  • immobility e.g. wheel chair use
  • carrier of known gene mutations associated with breast cancer (e.g. BRCA1/BRCA2)
  • current gallbladder disease
136
Q

UKMEC 4

A
  • > 35 years old and smoking more than 15 cigarettes/day
  • migraine with aura
  • history of thromboembolic disease or thrombogenic mutation
  • history of stroke or ischaemic heart disease
  • breast feeding < 6 weeks post-partum
  • uncontrolled hypertension
  • current breast cancer
  • major surgery with prolonged immobilisation
    positive antiphospholipid antibodies (e.g. in SLE)>
137
Q

Adenomyosis

A

presence of endometrial tissue within the myometrium. It is more common in multiparous women towards the end of their reproductive years.

138
Q

Features of Adenomyosis

A

dysmenorrhoea
menorrhagia
enlarged, boggy uterus

139
Q

Investigations of adneomyosis

A

NICE recommend transvaginal ultrasound as the first-line investigation
MRI is an alternative

140
Q

Managment of adenomyosis

A
  1. symptomatic treatment
    - tranexamic acid to manage menorrhagia
    - GnRH agonists
    - uterine artery embolisation
  2. considered the ‘definitive’ treatment
    - hysterectomy
141
Q

Primary amenorrhoea

A
  • failure to establish menstruation by 15 years of age in girls with normal secondary sexual characteristics (such as breast development), or by 13 years of age in girls with no secondary sexual characteristics
142
Q

Secondary amenorrhoea

A

cessation of menstruation for 3-6 months in women with previously normal and regular menses, or 6-12 months in women with previous oligomenorrhoea

143
Q

Causes of primary amenorrhoea (6)

A
  • gonadal dysgenesis (e.g. Turner’s syndrome) - the most common causes
  • testicular feminisation
  • congenital malformations of the genital tract
  • functional hypothalamic amenorrhoea (e.g. secondary to anorexia)
  • congenital adrenal hyperplasia
  • imperforate hymen
144
Q

Seondary amenorrhoea

A
  • pregnancy
  • hypothalamic amenorrhoea (e.g. secondary stress, excessive exercise)
  • polycystic ovarian syndrome (PCOS)
  • hyperprolactinaemia
  • premature ovarian failure
  • thyrotoxicosis*
  • Sheehan’s syndrome
  • Asherman’s syndrome (intrauterine adhesions)
145
Q

Primary managment of amenorrhoea

A
  • investigate and treat underlying cause
  • consider hormone replacement.
146
Q

Secondary amenorrhoea managment

A
  • exclude pregnancy, lactation, and menopause (in women 40 years of age or older)
  • treat the underlying cause
147
Q

Investigations of amenorrhoea

A
  • exculde pregancy
  • FBC, U+E, coeliac screen, thyroid functon
  • gonadotrophins
  • prolactin
  • oestradiol
  • androgen levels (PCOS concern)
148
Q

Amniotic fluid embolism

A

This occurs when fetal cells or amniotic fluid enter the mother’s bloodstream, triggering a reaction that leads to various signs and symptoms.

149
Q

Amniotic fluid embolism epidemiology

A

Rare complication of pregnancy
High mortality rate
Incidence: 2 per 100,000 in the U.K

150
Q

AFE aetiology

A
  • Clear cause not proven, but several risk factors identified
  • Associated with maternal age and induction of labor
    -Occurs when maternal circulation is exposed to fetal cells/amniotic fluid
  • Underlying pathology not well understood, possibly immune-mediate
151
Q

AFE clinical presentation

A
  • Often occurs during labor but can also happen during cesarean section or postpartum
  • Symptoms: Chills, shivering, sweating, anxiety, coughing
  • Signs: Cyanosis, hypotension, bronchospasms, tachycardia, arrhythmia, myocardial infarction
152
Q

Diagnosis of AFE

A

Clinical diagnosis of exclusion
No definitive diagnostic tests

153
Q

Managment of AFE

A

Requires care in a critical care unit
Managed by a multidisciplinary team
Predominantly supportive treatment

154
Q

Androgen Insensitivity Syndrome

A

An X-linked recessive condition caused by end-organ resistance to testosterone. Genotypically male children (46XY) present with a female phenotype. Complete androgen insensitivity syndrome is the modern term for testicular feminization syndrome.

155
Q

Features of AIS

A

Primary amenorrhea
Little or no axillary and pubic hair
Undescended testes causing groin swellings
Breast development may occur due to the conversion of testosterone to estradiol

156
Q

Diagnosis of AIS

A

Buccal smear or chromosomal analysis: reveals 46XY genotype
After puberty: testosterone concentrations in the high-normal to slightly elevated range for postpubertal males

157
Q

Diagnosis of AIS

A

Counseling: Raise the child as female
Bilateral orchidectomy: Due to increased risk of testicular cancer from undescended testes
Estrogen therapy

158
Q

Antenatal care nutitional supplements

A
  • Folic Acid: 400 mcg from before conception until 12 weeks to reduce neural tube defects; higher doses may be needed for women on antiepileptics
  • Iron: Not offered routinely
  • Vitamin A: Avoid intake above 700 mcg (teratogenic risk); avoid liver
  • Vitamin D: 10 mcg/day recommended; higher-risk women (darker skin or cultural clothing coverage) should be given special attention
159
Q

Alcohol antenatal

A
  • do not drink
160
Q

Smoking antenatal

A

Discuss risks like low birthweight and preterm birth
NRT: Can be used if women have stopped smoking; discuss risks/benefits
Varenicline/Bupropion: Not offered to pregnant or breastfeeding women

161
Q

Food acquired infections antenataly

A

Listeriosis: Avoid unpasteurized milk, ripened soft cheeses (e.g., Camembert, Brie, blue-veined), pâté, and undercooked meat
Salmonella: Avoid raw/partially cooked eggs and meat, especially poultry

162
Q

Air travel during pregnancy

A

> 37 weeks (singleton pregnancy, no risk factors): Avoid air travel
32 weeks (uncomplicated multiple pregnancies): Avoid air travel
Increased risk of venous thromboembolism (VTE); use correctly fitted compression stockings

163
Q

Exercise during pregnancy

A

Moderate exercise is safe; not associated with adverse outcomes
Avoid high-impact sports (risk of abdominal trauma) and scuba diving

164
Q

Tamoxifen (SERM)

A

Mechanism: Acts as an estrogen receptor antagonist and partial agonist
Use: Management of estrogen receptor-positive breast cancer

165
Q

Tamoxifen adverse effects

A

Menstrual disturbances: vaginal bleeding, amenorrhea
Hot flushes (3% of patients discontinue due to climacteric side effects)
Venous thromboembolism
Endometrial cancer

166
Q

Examples of aromatase inhibitors

A

Anastrozole, Letrozole

167
Q

Adverse effects of aromatase inhibitors

A

Osteoporosis (NICE recommends DEXA scan at initiation)
Hot flushes
Arthralgia, myalgia
Insomnia

168
Q

Aromatase inhibitors

A

Mechanism: Reduce peripheral estrogen synthesis
Use: ER-positive breast cancer in postmenopausal women (as aromatization is a major source of estrogen production)

169
Q
A
170
Q

What is a significant risk factor for developing venous thromboembolism (VTE)?

A

Pregnancy

Pregnancy increases the likelihood of VTE due to physiological changes and factors such as increased clotting factors.

171
Q

When should a risk assessment for VTE be completed during pregnancy?

A

At booking and on any subsequent hospital admission

This ensures ongoing evaluation of risk factors that may change over time.

172
Q

What is the protocol for a woman with a previous history of VTE during pregnancy?

A

Considered high risk and requires low molecular weight heparin throughout the antenatal period

Additionally, expert input is necessary for managing these patients.

173
Q

What factors may categorize a woman as intermediate risk for VTE?

A

Hospitalisation, surgery, co-morbidities, or thrombophilia

These conditions warrant consideration for antenatal prophylactic low molecular weight heparin.

174
Q

List some risk factors that increase the likelihood of developing VTE in pregnant women.

A
  • Body mass index > 30
  • Parity > 3
  • Smoker
  • Gross varicose veins
  • Current pre-eclampsia
  • Immobility
  • Family history of unprovoked VTE
  • Low risk thrombophilia
  • Multiple pregnancy
  • VF pregnancy

Identifying these factors helps in assessing the overall risk for VTE.

175
Q

True or False: A woman with a body mass index greater than 30 is at increased risk for VTE during pregnancy.

A

True

Higher body mass index is associated with increased venous stasis and clotting risk.

176
Q

Fill in the blank: A woman who is a _______ is at increased risk of VTE during pregnancy.

A

[Smoker]

Smoking is known to impair endothelial function and increase clot formation.

177
Q

What is the significance of a family history of unprovoked VTE in pregnancy risk assessment?

A

It increases the likelihood of developing VTE

Family history can indicate a genetic predisposition to thrombosis.

178
Q

What should be considered for a pregnant woman who is immobile?

A

Antenatal prophylactic low molecular weight heparin

Immobility is a known risk factor for venous thromboembolism.

179
Q

What is the treatment duration for low molecular weight heparin if there are four or more risk factors?

A

Continued until six weeks postnatal

Immediate treatment is warranted with low molecular weight heparin.

180
Q

When should low molecular weight heparin be initiated for women with three risk factors?

A

From 28 weeks and continued until six weeks postnatal

This is crucial for managing risk during pregnancy.

181
Q

What should be done if a diagnosis of DVT is made shortly before delivery?

A

Continue anticoagulation treatment for at least 3 months

This is similar to the protocol for other patients with provoked DVTs.

182
Q

What is the treatment of choice for VTE prophylaxis in pregnancy?

A

Low molecular weight heparin

It is preferred over other anticoagulants in this context.

183
Q

Which anticoagulants should be avoided in pregnancy?

A

Direct Oral Anticoagulants (DOACs) and warfarin

These medications pose risks during pregnancy.