Pregnancy and Prenatal Care Flashcards

1
Q

Duration of Pregnancy

A
  • Normal duration of pregnancy: 40 weeks (280 days)
  • Preterm birth: live birth before the completion of 37 weeks
  • Post-term birth: live birth after 42 weeks
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2
Q

Gravidity

A

the number of times a woman has been pregnant

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3
Q

parity

A

the number of times a woman has given birth

P1001

1 delivery

0

0 abortions

1 live birth

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4
Q

Trimester breakdown

A
  1. First trimester (week 1–13)
  2. Second trimester (week 14–26)
  3. Third trimester (week 27–40)
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5
Q

Day of implantation

A

Day 6

Implantation (embryology) of the blastocyst (most commonly into the anterior or posterior wall of the uterus); The trophoblast penetrates the endometrium.

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6
Q

When is embryogenesis?

A

weeks 3-8

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7
Q

When is fetogenesis?

A

from week 9 onward

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8
Q

Prenatal Counseling aim

A
  • Identifying and addressing any modifiable risk factors for the woman, future pregnancy, and the fetus
  • Educating a woman about the risk factors and options for their reduction or elimination
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9
Q

Prenatal Evaluation general medical conditions

A

General chronic diseases: review history and identify chronic medical conditions which may affect the pregnancy (e.g., hypothyroidism, diabetes mellitus, chronic hypertension, etc.)

  • Hypothyroidism
    • Treat women with elevated TSH
  • Diabetes mellitus
    • Aim for an HbA1c < 6.5%
  • Hypertension
    • Avoid using ACE inhibitors and angiotensin receptor blockers, as they are teratogenic.
  • Family history of heritable conditions: assess family history
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10
Q

Prenatal evaluation communicable diseases (HIV)

A
  • Screen all women for HIV.
  • Initiate antiretroviral therapy in all women with HIV.
  • Counsel women with HIV regarding the risk of vertical transmission.
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11
Q

Pregnancy and Immunizations

A

Measles, mumps, rubella and varicella

  • Screen all women for immunity with antibody titer.
  • Vaccinate all nonimmune women
  • Counsel to avoid conceiving 28 days after the last vaccine dose.

Influenza:

  • Administer annual influenza vaccination to all women.

Tdap

  • single dose between the 27th and 36th week of pregnancy
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12
Q

Lifestyle modifications for pregnancy

A
  • maintaining a normal body weight
  • moderate-intensity exercise

Nutrition

  • sufficient intake of macronutrients and micronutrients
  • 0.4 mg of folic acid daily, ideally 4 weeks prior to pregnancy and continue for at least the first 2–3 months of pregnancy

Substance use

  • smoking cessation and alcohol and drug use discontinuation
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13
Q

Clinical signs of early pregnancy

A
  • Hyperpigmentation of the areola and formation of linea nigra
  • Increased urinary frequency
  • Fatigue

abdominal cramps, fatigue, polyuria, amenorrhea, and a lower abdominal mass

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14
Q

Measurment of hCG

A
  1. Peaks at 10 weeks of gestation (peak value: ∼100,000 mlU/mL)
  2. Decreases During 2nd trimester
  3. Stabilizes During 3rd trimester
  • Urine beta-hCG test
    • Qualitative test; less sensitive
    • 14 days after fertilization
  • Serum beta-hCG test
    • (quantitative, high sensitivity)
    • 6–9 days (on average) after fertilization
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15
Q

Ultrasound findings in correlation to hCG

A

At 1,500–2,000 mlU/mL pregnancy is visible with transvaginal ultrasound

(if beta-hCG< 1000 mlU/mL, then do transvaginal ultrasound in 2-4 days, allowing enough time for hCG toreach 1500)

1500-2000

  • week 5
  • gestational sac

2500

  • week 5
  • yolk sac

5000

  • week 7
  • fetal pole

17000

  • week 10
  • fetal heartbeat
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16
Q

Gestational Age

A

the age (in weeks and days) of the fetus calculated from the first day of the last menstrual period

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17
Q

Conceptional Age

A

the age (in weeks and days) of the fetus calculated from the day of conception (fertilization)

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18
Q

Naegele’s Rule

A

First day of the last menstrual period + 7 days + 1 year - 3 months

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19
Q

Ultrasound calculation of due date

A
  • more accurate than Naegele’s rule
  • Measurement of the crown-rump length (CRL) in the first trimester
  • Approx. 5 cm at 12 weeks
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20
Q

Physiological changes during preganancy

Cardiovascular

A
  • ↑ Progesterone → ↓ vascular tone → ↓ peripheral vascular resistance (↓ afterload)
    • ↑ Cardiac output by up to 40% (↑ preload)
    • ↑ Stroke volume (by ∼ 10–30%)
    • ↑ Heart rate (by ∼ 12–18 bpm) → ↑ uterine perfusion
    • ↓ Mean arterial pressure
  • Innocent systolic murmur (due to increaded CO and plasma volume)
  • The apex beat is displaced upward.
  • Varicosity and edema of lower limbs
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21
Q

physiological changes during pregnancy

Respiratory

A
  • increased Oxygen consumption (by ∼ 20%)
  • decreased total lung capacity, residual volume, functional residual capacity, and expiratory reserve volume
  • increased Intra-abdominal pressure through uterine growth → dyspnea
  • Progesterone stimulates the respiratory centers in the brain → hyperventilation (aimed to eliminate fetal CO2 more efficiently) → physiological, chronic compensated respiratory alkalosis (high normal pH, low CO2, high bicarb)
    • ↑ Tidal volume (by ∼ 40%) → ↑ minute ventilation
    • ↓ PCO2 (∼ 30 mm Hg)
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22
Q

physiological changes during pregnancy

RENAL

A
  • ↑ GFR (↑CO=↑ renal perfusion) → ↓ BUN and creatinine
  • ↑ Aldosterone (activation of ↓RAAS by resistance) → ↑ plasma volume + hypernatremia
  • ↑ Glucose levels in urine
    • (increased glomerular filtration results in overload of the glucose carrier responsible for its resorption)
  • ↑ Urinary frequency
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23
Q

physiologic changes in pregnancy

endocrine

A
  • Human placental lactogen increases insulin levels and insulin resistance
  • ↑ Triglycerides and cholesterol (due to increased lipolysis and fat utilization)
  • Hyperplasia of lactotroph cells in the anterior pituitary → physiological enlargement of the pituitary gland
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24
Q

physiological changes in pregnancy

Hematologic

A
  1. ↑ Plasma volume → ↓ hematocrit particularly towards the end of pregnancy (30–34th week of gestation); dilutional anemia ; (minimal hemoglobin value is 11 g/dL)
  2. ↑ RBC count
  3. ↓ Platelet count
  4. ↑ WBC count
  5. ↓ Albumin
  6. ↑ Fibrinogen and factor VII, VIII, ↓ protein Shypercoagulability(to reduce the risk of intrapartum blood loss)
  7. ↑ Alkaline phosphatase
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25
physiological changes in preganancy gastrointestinal
* ↑ Salivation * ↓ Motility (due to progesterone) → constipation * Hemorrhoids (uterus presses against the pelvic veinsand vena cava, impairing venous return)
26
physiologic changes in pregnancy MSK
Increased lumbar lordosis and relaxation of the ligaments supporting the joints of the pelvic girdle can cause lower back pain
27
physoilogical changes in preganancy skin
* Spider angioma * Palmar erythema * Striae gravidarum * Hyperpigmentation: chloasma, linea nigra, hyperpigmentation of the nipples
28
physiological changes in pregnancy vulva and vigaina
Progesterone and estrogen increase vaginal blood supply, thereby increasing Bartholin gland secretions= increased vaginal discharge
29
Recomened Weight Gain during pregnancy
The recommendations are determined by the BMI prior to the pregnancy: * BMI \< 18.5 (underweight): 28–40 lb (12–18 kg) * BMI 18.5–24.9 (normal weight): 25–35 lb (11–16 kg) * BMI 25–29.9 (overweight): 15–25 lb (7–11 kg) * BMI ≥ 30 (obese): 11–20 lb (5–9 kg)' Approx. 2 lb in the first trimester and up to 1 lb per week in the second and third trimesters
30
Benefits of physical activity during pregnancy
1. weight control, 2. improved or maintained physical fitness, 3. ↓ risk of gestational diabetes, 4. ↓ risk of operative delivery, 5. ↓ risk of eclampsia, 6. improved psychological wellbeing 7. ↓ postpartum recovery time
31
Safe physical activities in pregnancy
1. Walking 2. Running or jogging\*\*\* 3. Swimming 4. Stationary cycling 5. Pilates 6. Yoga\*\* 7. Racquet sports\*\*\* 8. Strength training\*\*\* \* Avoid positions associated with ↓ venous return \*\*\* May be considered safe in women who took part in these exercises before
32
Unsafe physical activities in pregnancy
1. Contact sports (e.g., soccer, basketball) 2. Activities associated with a high risk of falling (e.g., snow skiing, water skiing, gymnastics, surfing) 3. Hot yoga 4. Hot Pilates 5. Skydiving 6. Scuba diving
33
Amntiotic fluid index
8-18 = normal, AFI ≤5 cm = oligohydramnios, AFI ≥24 cm = polyhydramnios.
34
Oligohydramnios
amount of amniotic fluid \< 500 mL in the third trimester Complications * Intrauterine growth restriction * Intrauterine compression and decreased amniotic fluid ingestion → **Potter sequence:** pulmonary hypoplasia (cause of death due to severe neonatal respiratory insufficiency), craniofacial abnormalities, limb anomalies
35
Polyhydramnios
excessive amniotic fluid volume (\> 2000 mL in the third trimester) Complications * Fetal malposition * Umbilical cord prolapse * Premature rupture of membranes * Premature uterine contractions * Premature birth
36
Oligohydramnios Fetal Etiologies
1. Urethral obstruction (e.g., posterior urethral valves) 2. Bilateral renal agenesis 3. Autosomal recessive polycystic kidney disease (ARPKD) 4. Chromosomal aberrations (e.g., trisomy 18) 5. Intrauterine infections (e.g., congenital TORCH infections) 6. In multiple pregnancies: twin-to-twin transfusion syndrome
37
oligohydramnios maternal etiologies
1. Late or post-term pregnancies (\> 42 weeks of gestation) 2. Placental insufficiency 3. Preeclampsia 4. Premature rupture of membranes
38
polyhydramnios fetal etiologies
1. Gastrointestinal anomalies (e.g., esophageal atresia, duodenal atresia and stenosis) 2. CNS anomalies (e.g., anencephaly , meningomyelocele ) 3. Chromosomal aberrations 4. Intrauterine infections (e.g., congenital TORCH infections) 5. Multiple pregnancy: twin-to-twin transfusion syndrome
39
polyhydramnios maternal etiologies
1. Diabetes mellitus (increased fetal glucose levels, resulting in polyuria) 2. Rhesus incompatibility: hemolytic disease of the newborn
40
Predisposing factors for multiple pregnancy
* Advanced maternal age (\> 35 years) * Previous multiple pregnancy * Use of fertility enhancing treatments * Maternal family history of dizygotic twins
41
Monozygotic twins
* 1/3 twin pregnancies * division of fertilized oocyte * **genetically identical**
42
Dizygotic twins
* 2/3 of twin pregnancies * two oocyted with two spermatozoa * **genetically different** * **Dichorionic- diamniotic**
43
Dichorionic- diamniotic
Each twin has an individual amniotic sac and placenta.
44
Monochorionic- diamniotic
The twins **share a placenta** and have individual amniotic sacs. (twin-to-twin transfusion syndrome)
45
monochotionic- monoamniotic
The twins **share both** the placenta and amniotic sac.
46
Exam findings multiple pragnancy
* Fundal height and abdominal girth are unusually large for the gestational age * Two or more fetal heart rates can be heard on auscultation
47
Ultrasound multiple pregnancy
* Dichorionic twins: lambda sign * Separation of the chorionic and amniotic sacs resembles the Greek symbol "λ = lambda" * Monochorionic twins: T-sign * Separation of the amniotic sacs resembles a "T" on ultrasound.
48
Maternal complications of a multiple preganancy
1. Hyperemesis gravidarum and gestational diabetes 2. preeclampsia 3. **Cervical incompetence, premature birth, preterm labor, premature rupture of membranes** 4. Placental insufficiency 5. Uterine atony
49
Fetal complications of a multiple preganancy: Twin-to-twin transfusion syndrome
* Blood is continuously shunted from one twin to the other through vascular anastomoses on the shared placenta * Recipient twin: **polycythemia; polyhydramnios** in diamniotic pregnancies * Donor twin: **anemia**, dehydration, **growth retardation; oligohydramnios i**n diamniotic pregnancies
50
Ectopic pregnancy
a pregnancy in which the fertilized egg attaches in a location other than the endometrium * Tubal pregnancy: occurs within the fallopian tube- most common * Complicated ectopic pregnancy: associated with severe bleeding, rupture, or hemodynamic compromise. * Interstitial pregnancy: within the interstitial portion of the fallopian tube (connects the tube to the endometrial cavity)
51
Location of ectiopic cases
1. Fallopian tube (96% of cases): ampulla \>\> other 2. Ovary (3% of cases) 3. Abdomen (1% of cases) 4. Cervix (very rare)
52
Risk factors for ectopic preganancy
Anatomic alteration of the fallopian tubes: * A history of PID * Previous ectopic pregnancy * Past surgeries involving the fallopian tubes * Endometriosis Non‑anatomical risk factors * History of infertility * IUD (implantations outside uterus)
53
Clinical features of ectopic preganancy
* 4–6 weeks after their last menstrual period * Lower abdominal pain and guarding * **Vaginal bleeding** (mistaken for menstrations) * **Signs of pregnancy**: amenorrhea, nausea, breast tenderness, frequent urination * Tenderness in the area of the ectopic pregnancy * Cervical motion tenderness, **closed cervix** * **Enlarged uterus** * Interstitial pregnancies tend to present late, at 7–12 weeks of gestation, because of myometrial distensibility
54
clincal features of tubal rupture
* Acute course with sudden and severe lower abdominal pain (acute abdomen) * Signs of hemorrhagic shock: e.g., tachycardia, hypotension, syncope * More common in interstitial pregnancy
55
hCG in ectopic preganancy
Serial β-hCG measurements(48 hours) * Intrauterine pregnancies: β-hCG increases by ≥ 50% in 99% of patients. * **Ectopic pregnancies:** Approx. 70% of patients show an insufficient increase or decrease of β-hCG.
56
Ectopic Pregnancy diagnostics
**Transvaginal ultrasound (TVUS)** * best initial imaging test * Empty uterine cavity in combination with a thickened endometrial lining * Possible free fluid within the pouch of Douglas * Tubal ring sign * Interstitial line sign * A thin myometrial layer (\< 5 mm) surrounding the gestational sac
57
tubal ring sign
an echogenic ring that surrounds an unruptured ectopic pregnancy
58
interstitial line sign
an echogenic line that extends from the gestational sac into the upper uterus
59
treatment ectopic pregnancy
* uncomplicated: methotrexate * hemodynamically unstable or signs or rupture 1. fluid resuscitation normal saline or lactated Ringer's solution * Hgb \>10 no blood even if in shock 2. salpingostomy
60
Differential Painful Vaginal Bleeding
1. Ectopic pregnancy * Lower unilateral abdominal pain and guarding * Positive pregnancy test * Ultrasound shows echogenic mass. 2. Benign neoplasms * chronic pelvic or back pain/discomfort * irregularly enlarged uterus, infertility 3. Ovarian cyst rupture * Sudden onset of unilateral abdominal pain * Onset usually during physical activity 4. Infection/Inflammation (PID, cervicitis) * lower bilateral abdominal pain/ lower abdominal or pelvic pain * fever, dyspareunia, purulent cervical discharge 5. Endometriosis * Chronic pelvic pain that worsens before the onset of menses * Dysmenorrhea Dyspareunia 6. Trauma * Pelvic pain
61
Differential Painless Vaginal Bleeding
1. PCOS * _Amenorrhea, oligomenorrhea_ * _Hirsutism, obesity, acne vulgaris, infertility_ * Ultrasound shows _enlarged ovaries_ with numerous anechoic cysts. 2. Endometrial hyperplasia * Constant bleeding * Ultrasonography- _endometrial thickening._ 3. Endometrial polyp * Irregular menstrual bleeding 4. Malignant neoplasms * _Cervical cancer:_ menometrorrhagia, postcoital spotting, _abnormal vaginal discharge_ * _Endometrial cancer:_ metrorrhagia, menometrorrhagia
62
Frequency of Prental check up
1. Until the 28th week of pregnancy: monthly 2. From the 28th week until the 36th week: every two weeks 3. From the 36th week until birth: every week
63
Initial Pregnency encounter
1. Personal and family history, previous pregnancies 2. Gynecological examination 3. Laboratory analysis 4. Ultrasound assessment
64
STD test in pregnancy
* HIV (using 3rd or 4th generation ELISA), * syphilis(using nontreponemal tests such as VDRL or RPR), * hepatitis B infection (using HBsAg). * \< 25 years, have risk factor: Chlamydia and N. gonorrhea infection by PCR of vaginal swabs
65
Initial lab analysis for preganancy
1. CBC 2. Anemia 3. Blood typing (ABO and rhesus) 4. Proteinuria 5. Asymptomatic bacteriuria 6. Screening for STIs * HIV testing * Syphilis screening * Hepatitis B surface antigen testing * Chlamydia testing: * \< 25 years of age and ≥ 25 years with high risk of infection 7. Rubella and varicella antibody testing
66
Follow Up Preganancy encounters
1. Blood pressure monitoring: early detection of pregnancy-induced hypertension 2. First-trimester screening: screening of chromosomopathies 3. Physical examination * Leopold's maneuver * Fetal heart monitoring 4. Laboratory
67
Follow up encounter Labs for preganancy
1. Group B streptococcus screening performed between **36 0/7 and 37 6/7 weeks** of gestation 2. Repeat Hb from the **24th week** 3. 50-g, one-hour oral glucose challenge test (initial screening) at **24–28** weeks gestation * 100-g, three-hour oral glucose tolerance test to confirm diagnosis 4. Repeat rhesus screening
68
Group B Screening
* vaginal and rectal swab for culture and gram staining * colonization by this bacteria may cause chorioamnionitisand neonatal infection.
69
Leopold Maneuver
1. First: bimanual examination of the **fetal position** (longitudinal/oblique/transverse) and **fundal height** 2. Second: bimanual examination of the **location of the fetal back** (i.e., either on the mother's left or right side) 3. Third: One hand **grasps above the symphysis** in an attempt to **determine if the presenting part of the fetus is engaged.** 4. Fourth: Bimanual determination of the location of the fetal brow and the degree of flexion of the fetus's head. when the fetus has entered the pelvic inlet.
70
Fundal Height
increases ∼ 1 cm/week in the second and third trimester. * Week 12 = Just above the symphysis * week 20 = Between the symphysis and navel * week 24 = Navel * week 32 = Between the navel and xiphoid * week 36 = Peak: at the costal arch * week 40 = Two finger widths below the costal arch
71
Prenatal diagnostics
All pregnant women (regardless of age) should be offered noninvasive aneuploidy screening tests (before 20 weeks gestation) * Possible tests: * Testing maternal serum; specific biomarkers and ultrasound * Cell-free fetal DNA testing * invasive genetic testing; amniocentesis or CVS
72
Noninvasive screening tests: First trimenster combinded screaning (11-13wks)
* Sonographic nuchal translucency (NT) * β-HCG in maternal serum * PAPP-A in maternal serum Detects: 1. **Down syndrome/Trisomy 21**: ↑ HCG, ↓ PAPP-A, ↑NT 2. Trisomy 18 & 13: ↓ HCG, ↓↓ PAPP-A, ↑ NT 3. Molar pregnancy: ↑↑ HCG 4. Ectopic pregnancy: ↓ HCG 5. **Neural tube defects**: ↑ HCG
73
Noninvasive screening tests: Triple Screen (15-20wks)
* based on maternal age and ultrasound * HCG * Alpha-fetoprotein(AFP) * Estriol Diagnoses: 1. **Trisomy 21:** ↑ β-HCG, ↓ AFP, ↓ free estriol, ↑ Inh A 2. Trisomy 18: ↓↓ β-HCG, ↓ AFP, ↓↓ free estriol,↔︎ or ↓ Inh A 3. Molar pregnancy: ↑↑ HCG 4. Ectopic pregnancy: ↓ HCG, ↓ AFP, ↓ free estriol 5. **Neural tube defects:** ↔︎ HCG, ↑ AFP, ↔︎ free estriol, ↔︎ inh A 6. Abdominal wall defects: ↔︎ HCG, ↑ AFP, ↔︎ free estriol, ↔︎ inh A
74
Noninvasive screening tests: Quad Screen (15-20wks)
* based on maternal age and ultrasound * HCG * Alpha-fetoprotein(AFP) * Estriol * Inhibin A (Inh A) Diagnoses: 1. **Trisomy 21:** ↑ β-HCG, ↓ AFP, ↓ free estriol, ↑ Inh A 2. Trisomy 18: ↓↓ β-HCG, ↓ AFP, ↓↓ free estriol,↔︎ or ↓ Inh A 3. Molar pregnancy: ↑↑ HCG 4. Ectopic pregnancy: ↓ HCG, ↓ AFP, ↓ free estriol 5. **Neural tube defects:** ↔︎ HCG, ↑ AFP, ↔︎ free estriol, ↔︎ inh A 6. Abdominal wall defects: ↔︎ HCG, ↑ AFP, ↔︎ free estriol, ↔︎ inh A
75
Noninvasive screening twsts: Sequential integrated tests
1. Frist trimerster combined (10-13 wks) 2. Quad screen test (15-20 wks)
76
Noninvasive screen tests: cell free fetal DNA testing (cffDNA)- 10wks +
* Fetal DNA is isolated from a maternal blood specimen for genetic testing' Detects: 1. Identifies chromosomal aberrations * (high specificity and sensitivity for trisomy 21 \> trisomy 18 \>trisomy 13) 2. Determine the sex of the fetus 3. high sensitivity (\> 99%) and specificity (\> 99%) for Down syndrome
77
Invasive diagnostic tests: Chorionic Villus Sampling (10-13 wks)
* removal of chorionic tissue under sonographic guidance * Analysis of DNA for genetic diagnosis in early pregnancy * preferred testing method before 15wks for prenatal genetic diagnosis (conformatory) * perform after 1st trimester screening Complications: 1. Miscarriage(approximate risk: 2–3%) 2. Limb defects
78
invasive diagnostic tests: amniocentesis (15 wks +)
* AF is extracted under sonographicguidance via transabdominal puncture Comlications 1. Miscarriage(approximate risk: 0.5–1%) 2. **Premature rupture of the membranes** 3. Infection
79
Invasive diagnostic testing: cordocentesis (17wks +)
* Fetal blood sampling via ultrasound-guided transabdominal needle insertion into the umbilical cord * dentify the type of fetal hemoglobinand to assess the severity of fetal anemia Complications 1. miscarriage 2. infection
80
Doppler Ultrasound indications
* Suspected intrauterine growth restriction * Suspected fetal deformities * Growth discordance in multiple pregnancies
81
doppler ultrasound findings
1. Uterine artery * Early diastolic notch * risk of preeclampsiaand/or fetal growth restriction 2. Umbilical artery * Decline or loss of end diastolic flow velocity or negative flow * increased resistance to the placentalvascular bed 3. Fetal middle cerebral artery * Increased diastolic flow velocity * centralization ("brain sparing effect") in fetal hypoxia
82
Antepartum fetal surveillance
1. Nonstress Test (NST) 2. Contraction stress test (CST) 3. Biophysical Profile (BPP)
83
Nonstress Test
* a noninvasive test cardiotography (CTG) that measures FHR reactivity to fetal movements * Indications: * maternal medical conditions (e.g., gestational diabetes, preeclampsia) * fetal conditions (e.g., fetal heart defects, fetal growth restriction) * performed in the third trimester
84
Nonstress Test Findings
1. A normal NST would show ≥ 2 FHR accelerations. 2. Reactive nonstress test: normal 3. Non-reactive nonstress test: \<2 FHR accelerations 1. Perform vibroacoustic stimulation 2. If the NST is still non-reactive: check the biophysical profile (BPP) or perform contraction stress test
85
Contraction Stress test (CST)
* measures FHR reactivity in response to uterine contractions * contractions are stimulated with oxytocin administration.
86
Biophysical Profile (BPP)
evaluates the risk of antenatal fetal death. Ultrasound exam. Measured parameters: 0 (abnormal) or 2 (normal) 1. Fetal movement 2. Fetal tone 3. Fetal breathing 4. Amniotic fluid volume ≥ 8 points: no signs of fetal compromise at the time of testing ≤ 4 points: potential fetal compromise → **delivery is indicated**
87
BPP Parameters
1. Fetal movement * ≥ 3 body or limb movements within a 30-minute period 2. Fetal tone * ≥ 1 episodes of a fetal extremity or fetal spine extension with return to flexion 3. Fetal breathing * ≥ 1 rhythmic breathing episode(s) ≥ 30 seconds within a 30-minute period 4. Amniotic fluid volume * A single deepest vertical pocket ≥ 2 cm 5. Nonstress test * ≥ 2 episodes of FHR accelerations
88
HIV in pregnancy transmission
* Highest risk during birth (perinatal vertical transmission) * Prenatal transmission is possible * **Risk depends on maternal viral load**
89
HIV in preganancy: reducing risk of transmition
1. Combined antiretroviral therapy (cART) is recommended throughout pregnancy 2. Delivery method Viral load \> 1,000 copies/mL: increased risk of HIV transmission * Cesarean delivery should be scheduled at 38 weeks * post-exposure prophylaxis with **zidovudine, lamivudine and nevirapine OR zidovudine and nevirapine** 3. Viral load ≤ 1,000 copies/mL and mother has received cART * HIV post-exposure prophylaxis with **zidovudine** for the newborn * vaginal delivery considered 4. Breastfeeding should generally be avoided , because risk of transmission is 5–20%
90
HIV in preganancy: Diagnosis in infants
if \< 18 months, diagnosis is confirmed via PCR, not ELISA
91
Anti-D immunoglobulin (RhoGAM)
* An antibody against the rhesus D antigen that is used as prophylaxis against hemolytic disease of the fetus and newborn in Rh(D) negative mothers. * Anti-D prophylaxis protects newborns in subsequent pregnancies. * Only indicated in unsensitized mothers
92
Anti-D immunoglobulin indication and implementation
Anti-D prophylaxis should be administered during the **28th week** of gestation and **within 72 hours** following the birth of an Rh-positive baby. Further indicaitons: 1. Following a miscarriage, ectopic pregnancy, or termination of pregnancy 2. Bleeding during pregnancy 3. Following invasive procedures (e.g., amniocentesis, chorionic villus sampling
93
RH negative mothers
1. No anti-D antibodies (**unsensitized** mothers): antibody screening repeated at 28 weeks' gestation and at delivery. 2. Anti-D antibodies manifest with an anti-D antibody titer \> 1:8, which indicates maternal sensitization to fetal Rh antigens (**sensitized** mothers). * Further monitoring with amniocentesis and imaging is required for evidence of hemolysis.
94
Fetomaternal Hemorrahe in Rh- negative mother
1. Conduct a rosette test (initial test of choice). This is a qualitative test that assesses whether fetomaternal hemorrhage has occurred. 2. If the rosette test is positive, conduct a Kleihauer-Betke test. * The amount of fetal hemoglobin determines the amount of Anti-D immunoglobulin necessary.
95
Rosette Test
Maternal Rh-negative blood is incubated with Rho(D) immunoglobulin, which binds to fetal Rh-positive erythrocytes. The addition of an indicator causes these erythrocytes to form a rosette pattern
96
Kleihauer Betke Test
maternal blood smear is exposed to acid and then stained. Adult hemoglobin is removed by the acid whereas fetal hemoglobin (HbF) is not, thus, cells appear pink on a positive test for fetal hemoglobin
97
Birth weight
* very low 1000-1499 * low: \<2500g * Normal: 2500-4000g * Macrosomic: 4500g