Translate these into English and answer the questions
~/attachments/87c7e76d-1748-4e43-b2ef-99dfcc53a043
python3 -c "from docx import Document; p='/tmp/workspace/attachments/87c7e76d-1748-4e43-b2ef-99dfcc53a043/1. Вопросы к Перевод экз. 25-26 ч.г..docx'; d=Document(p); [print(x.text) for x in d.paragraphs if x.text.strip()]; [print(' | '.join(c.text for c in r.cells)) for t in d.tables for r in t.rows]"
Choose the section to translate and answer in detail first.
Do obstetrics first
Translate and answer all 64 obstetrics questions
Which obstetrics module should I translate and answer first?
Make a concise obstetrics oral-exam answer sheet
pregnancy complications
WHO recommendations maternal and perinatal health pregnancy childbirth postpartum haemorrhage preeclampsia
Quick answer
Lets do one thing I have my obgy examination and I want to prepare for that exam so lets answer 5 questions at a time Make sure you are accurate and teach me all the topics in examination point of view
Start with obstetrics Questions 1–5
polyhydramnios oligohydramnios
WHO perinatal mortality definition stillbirth early neonatal death 2025 antenatal care fetal assessment
site:consultant.ru Приказ Минздрава 1130н 20.10.2020 порядок оказания медицинской помощи акушерство гинекология структура родильного дома
| Ovarian cycle | Endometrial cycle | Main hormonal event |
|---|---|---|
| Follicular phase | Menstrual then proliferative phase | FSH stimulates follicle development; estrogen rises |
| Ovulation | Late proliferative phase | LH surge causes rupture of dominant follicle |
| Luteal phase | Secretory phase | Progesterone from corpus luteum predominates |
Give me Questions 6–10 in the same format
breech presentation delivery
ACOG Rh D alloimmunization pregnancy breech presentation external cephalic version guidance
| Hormone | Main source | Main actions |
|---|---|---|
| hCG | Syncytiotrophoblast | Maintains corpus luteum in early pregnancy; stimulates progesterone production |
| Progesterone | Corpus luteum initially, then placenta | Maintains decidua, decreases myometrial activity, relaxes smooth muscle, supports pregnancy |
| Estrogens | Fetoplacental unit | Uterine growth, breast development, increased uterine blood flow, prepares myometrium for labor |
| Human placental lactogen, hPL | Placenta | Produces maternal insulin resistance and lipolysis, preserving glucose for fetus |
| Relaxin | Corpus luteum and placenta | Softens connective tissue, contributes to pelvic and cervical changes |
| Prolactin | Maternal anterior pituitary | Prepares breast for milk production |
| Oxytocin | Maternal posterior pituitary | Uterine contractions and milk ejection; receptor expression rises near term |
Give me Obstetrics Questions 11–15 in the same format
intrapartum vaginal examination labor
WHO intrapartum care vaginal examination every four hours recommendations
| Germ layer | Major derivatives |
|---|---|
| Ectoderm | Nervous system, epidermis, sense organs |
| Mesoderm | Muscle, bone, connective tissue, heart, blood, kidneys, gonads |
| Endoderm | Epithelium of gastrointestinal and respiratory tracts, liver, pancreas |
| Measurement | Approximate normal value |
|---|---|
| Distantia spinarum: distance between anterior superior iliac spines | 25-26 cm |
| Distantia cristarum: distance between iliac crests | 28-29 cm |
| Distantia trochanterica: distance between greater trochanters | 31-32 cm |
| External conjugate, Baudelocque diameter | 20-21 cm |
| Diameter | Approximate value |
|---|---|
| Anatomical conjugate | 11.5 cm |
| Obstetric conjugate | 10.5-11 cm |
| Diagonal conjugate | 12.5-13 cm |
| Transverse diameter | 13-13.5 cm |
| Oblique diameter | 12-12.5 cm |
| Type | Features |
|---|---|
| Gynecoid | Rounded inlet, wide subpubic angle; most favorable for vaginal birth |
| Android | Heart-shaped inlet, narrow anterior pelvis; may predispose to deep transverse arrest |
| Anthropoid | Oval inlet with long anteroposterior diameter; occiput-posterior positions more common |
| Platypelloid | Flattened pelvis with wide transverse and short AP diameter; engagement may be difficult |
| Suture | Location |
|---|---|
| Sagittal suture | Between the two parietal bones |
| Coronal sutures | Between frontal and parietal bones |
| Frontal or metopic suture | Between the two frontal bones |
| Lambdoid sutures | Between parietal bones and occipital bone |
| Diameter | Extent | Approximate size | Presentation |
|---|---|---|---|
| Suboccipitobregmatic | Nape of neck to center of bregma | 9.5 cm | Well-flexed vertex |
| Suboccipitofrontal | Nape of neck to frontal eminence | 10 cm | Incomplete flexion |
| Occipitofrontal | Occiput to glabella | 11.5 cm | Deflexed vertex |
| Mentovertical | Chin to highest point of vertex | 13.5 cm | Brow presentation |
| Submentobregmatic | Junction of neck and chin to bregma | 9.5 cm | Face presentation with complete extension |
| Bitemporal | Between temporal bones | 8 cm | Transverse diameter |
| Biparietal | Between parietal eminences | 9.5 cm | Largest transverse diameter |
| Circumference | Approximate value |
|---|---|
| Suboccipitobregmatic | 32 cm |
| Occipitofrontal | 34 cm |
| Mentovertical | 35-36 cm |
| Submentobregmatic | 32 cm |
Give me Questions 16–20 in the same format
labor management second stage
WHO intrapartum care stages labour second stage birth perineal techniques recommendations
| Stage | Nulliparous woman | Multiparous woman |
|---|---|---|
| First stage | Up to about 12-18 hours | Up to about 8-12 hours |
| Second stage | Usually up to about 2 hours without epidural, may be longer with epidural | Usually up to about 1 hour without epidural, may be longer with epidural |
| Third stage | Usually within 30 minutes | Usually within 30 minutes |
| Feature | Primiparous woman | Multiparous woman |
|---|---|---|
| Cervical effacement | Usually precedes dilation | Often occurs with dilation |
| First stage duration | Usually longer | Usually shorter |
| Cervical dilation | Generally slower | Generally faster |
| Fetal head engagement | Often occurs before labor or early in labor | May occur later, even during labor |
Give me Obstetrics Questions 21–25 in the same format
postpartum hemorrhage episiotomy
WHO postpartum haemorrhage blood loss objective measurement active management third stage labour postpartum care guideline
| Feature | Caput succedaneum | Cephalohematoma | Subgaleal hemorrhage |
|---|---|---|---|
| Site | Subcutaneous scalp tissue | Beneath periosteum | Potential space beneath galea |
| Crosses sutures? | Yes | No | Yes, widely |
| Time of appearance | At birth | Usually hours after birth | May become evident after birth |
| Consistency | Soft, pitting edema | Firm, localized swelling | Diffuse, boggy, fluctuant |
| Importance | Usually benign | May cause jaundice/anemia | Potentially life-threatening hemorrhage |
Treat the woman, not only the number of milliliters.
| Cause | Examples |
|---|---|
| Tone | Uterine atony |
| Trauma | Cervical, vaginal, perineal tears; uterine rupture |
| Tissue | Retained placenta, retained membranes, placenta accreta spectrum |
| Thrombin | Coagulopathy, DIC |
| Type | Typical period | Appearance |
|---|---|---|
| Lochia rubra | Days 1-3/4 | Red, bloody |
| Lochia serosa | Days 4-10 | Pinkish or brown |
| Lochia alba | From about day 10 to 4-6 weeks | Yellowish-white |
If I asked you to create a pdf of whole 1 to 64 questions Would you give me with exact this much detailed answer without compromising the quality?
Create the complete Obstetrics Questions 1–64 PDF
~/
preeclampsia postpartum hemorrhage obstetric sepsis
WHO maternal perinatal health guidelines preeclampsia postpartum haemorrhage preterm birth obstetric sepsis 2025
mkdir -p "/tmp/workspace/obstetrics-oral-exam-pdf/src" "/tmp/workspace/obstetrics-oral-exam-pdf/output"
~/obstetrics-oral-exam-pdf/src/create_pdf.py
from reportlab.lib import colors
from reportlab.lib.enums import TA_CENTER
from reportlab.lib.pagesizes import A4
from reportlab.lib.styles import getSampleStyleSheet, ParagraphStyle
from reportlab.lib.units import cm
from reportlab.platypus import SimpleDocTemplate, Paragraph, Spacer, PageBreak, Table, TableStyle, KeepTogether
from reportlab.pdfbase import pdfmetrics
from reportlab.pdfbase.ttfonts import TTFont
from reportlab.lib.colors import HexColor
from xml.sax.saxutils import escape
import os
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styles=getSampleStyleSheet()
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# Each entry: question title, translated question, structured oral answer, examiner points.
Q = [
('1. Organization of obstetric care','Types of obstetric inpatient facilities. Structure of a city maternity hospital. Main performance indicators.','<b>System.</b> Care is regionalized into antenatal clinics, level I maternity units for low-risk births, level II hospitals for moderate risk, and level III perinatal centres for severe maternal disease, very preterm birth and neonatal intensive care. <b>Structure.</b> Admission/triage, antenatal pathology ward, labor rooms, operating theatre, anesthesia and ICU, postpartum wards, neonatal service, laboratory, imaging, transfusion access and infection-control areas. <b>Indicators.</b> Maternal mortality, perinatal mortality, stillbirth, early neonatal death, severe maternal morbidity, cesarean rate, PPH, eclampsia, sepsis, prematurity, low birth weight, infection, bed occupancy and referral rate.','State the principle: the right woman and fetus must be delivered at the right level of care. A cesarean rate alone is not a quality indicator.'),
('2. Perinatal period and fetal surveillance','Definition, rate, structure, causes of perinatal mortality; modern assessment of the fetus in utero.','<b>Definition.</b> For international reporting, perinatal mortality includes late fetal deaths from 28 completed weeks and early neonatal deaths on days 0-6. <b>Formula.</b> (late fetal deaths + early neonatal deaths) / (live births + late fetal deaths) x 1000. <b>Structure.</b> Antepartum stillbirth, intrapartum stillbirth and early neonatal death. <b>Causes.</b> Prematurity, congenital anomalies, placental insufficiency/FGR, hypoxia, infection, maternal hypertension/diabetes and intrapartum events. <b>Assessment.</b> Maternal movement history, ultrasound anatomy/biometry/fluid, Doppler, CTG and biophysical profile.','Perinatal mortality measures both obstetric and neonatal care. Never interpret CTG in isolation.'),
('3. Female reproductive anatomy and physiology','Anatomy and physiology of the female reproductive system.','<b>Anatomy.</b> Internal organs are ovaries, tubes, uterus, cervix and vagina; external organs form the vulva. The uterine wall comprises endometrium, myometrium and perimetrium. Fertilization usually occurs in the ampulla. <b>Axis.</b> Pulsatile GnRH stimulates FSH and LH. Estrogen drives follicular/endometrial proliferation; an LH surge triggers ovulation; the corpus luteum secretes progesterone, producing secretory endometrium. <b>Supports.</b> Levator ani, endopelvic fascia, uterosacral and cardinal ligaments support uterus and vagina.','Ovulation is about 14 days before the next menses, not always cycle day 14. The myometrium is the contractile layer.'),
('4. Polyhydramnios and oligohydramnios','Amniotic-fluid turnover, etiology, diagnosis, and management of pregnancy and labor.','Fluid is produced mainly by fetal urine and lung fluid; removed by swallowing and intramembranous absorption. <b>Polyhydramnios:</b> DVP at least 8 cm or AFI about 24-25 cm or more. Causes: diabetes, impaired swallowing from anomaly, anemia/hydrops, TTTS, or idiopathic. Risks: preterm labor, malpresentation, cord prolapse, abruption after rapid decompression and atony. <b>Oligohydramnios:</b> DVP below 2 cm or AFI 5 cm or less. Causes: PPROM, placental insufficiency/FGR, post-term pregnancy, renal anomaly or drugs. Assess anatomy, growth, Dopplers, membranes and maternal disease; surveillance and delivery timing depend on gestation and fetal status.','Polyhydramnios = excess production or reduced swallowing. Oligohydramnios = membrane rupture, low placental perfusion or low fetal urine.'),
('5. Diagnosis of pregnancy and fetal weight','Diagnosis of early and late pregnancy. Methods of antenatal estimation of fetal weight.','<b>Presumptive signs:</b> amenorrhea, nausea, breast change, quickening. <b>Probable signs:</b> hCG, uterine enlargement, Goodell/Hegar/Chadwick signs. <b>Diagnostic signs:</b> embryo/fetus or cardiac activity on ultrasound, fetal heart heard by Doppler, movements palpated by examiner. Use LMP and first-trimester crown-rump length for dating. <b>EFW.</b> Clinical: fundal height and palpation. Ultrasound: HC/BPD, AC and FL in validated formulas, commonly Hadlock. It is an estimate with clinically important error, often about 10 percent.','Positive hCG does not establish location or viability. First-trimester ultrasound is best for dating.'),
('6. Hemolytic disease of fetus and newborn','Etiology, pathogenesis, clinical forms and treatment.','HDFN is maternal IgG-mediated destruction of antigen-positive fetal red cells. Major antibodies: anti-D, anti-c and anti-Kell; ABO disease is usually neonatal and milder. Sensitization follows delivery, miscarriage, bleeding, trauma, invasive procedures or incompatible transfusion. Hemolysis causes anemia, hepatosplenomegaly, high-output failure and hydrops; after birth it causes jaundice and risk of kernicterus. Screen maternal group/Rh and antibodies; identify antibody and fetal antigen; use MCA-PSV Doppler for fetal anemia. Treatment: specialist intrauterine transfusion if severe; neonatal phototherapy, IVIG in selected cases, transfusion/exchange transfusion.','Anti-D immunoglobulin prevents sensitization in unsensitized RhD-negative women. It does not treat established alloimmunization.'),
('7. Maternal physiological changes','Physiological maternal changes in pregnancy. Hormonal regulation of gestation.','<b>CV:</b> plasma volume rises more than red-cell mass causing dilutional anemia; cardiac output and heart rate rise; SVR and mid-pregnancy BP fall. <b>Respiratory:</b> progesterone raises minute ventilation; FRC falls, causing mild compensated respiratory alkalosis. <b>Renal:</b> GFR rises, so creatinine is normally lower; ureteric dilatation predisposes to UTI. <b>Metabolic:</b> increasing late insulin resistance and hypercoagulability. <b>Hormones:</b> hCG sustains corpus luteum; progesterone maintains quiescence; estrogens promote uterine growth; hPL causes insulin resistance; prolactin prepares breast; oxytocin acts in labor/lactation.','Pregnancy is hypercoagulable. A creatinine that appears normal for a non-pregnant adult can be abnormal in pregnancy.'),
('8. Breech presentation','Causes, classification, diagnosis, and management of pregnancy.','Breech is a longitudinal lie with buttocks or feet at the inlet. Types: frank, complete and incomplete/footling. Risks: prematurity, uterine anomaly/fibroid, placenta previa, abnormal fluid, multiple pregnancy and fetal anomaly. Diagnose by Leopold maneuvers and confirm with ultrasound: type, fetal head attitude, growth, placenta, fluid and anomaly. Most early breeches turn. At 36-37 weeks, consider external cephalic version if no contraindication. Persistent term singleton breech usually has planned cesarean; vaginal breech birth is reserved for strict selection and an experienced team with immediate cesarean capability.','Frank breech is commonest at term. Footling breech has high cord-prolapse risk.'),
('9. Placenta as endocrine organ','Physiology of pregnancy. Placenta as a new endocrine gland: definition, functions and structure.','The placenta is a temporary fetomaternal organ: fetal chorionic villi are bathed in maternal blood in the intervillous space. Functions are gas exchange, nutrient/waste transfer, metabolism, immune modulation and hormone production. It produces hCG, progesterone, estrogens, hPL, placental GH, CRH, inhibin and prostaglandins. hCG supports the early corpus luteum; progesterone supports decidua and quiescence; estrogens promote uterine growth and labor readiness; hPL diverts maternal fuels toward the fetus. Umbilical arteries carry deoxygenated fetal blood to placenta; one umbilical vein returns oxygenated blood.','Maternal and fetal blood normally do not mix directly. The placenta is selective, not an absolute barrier.'),
('10. Breech labor mechanism and management','Biomechanism of labor in breech presentation. Contemporary principles of labor management.','The sacrum is the denominator. Sequence: buttocks/pelvis, trunk, shoulders/arms, then after-coming head. The bitrochanteric diameter enters obliquely, sacrum rotates anteriorly, hips and trunk deliver by lateral flexion, shoulders rotate, then the flexed head enters and delivers by flexion. Management: pre-labor ultrasound and consent; continuous fetal monitoring; no traction before spontaneous descent; full dilation before active assistance; experienced operator, anesthesia and neonatal team available. Cesarean is indicated for fetal compromise, footling, hyperextended head, disproportion, anomaly or absent skilled team.','Key danger: cord compression and entrapment of the after-coming head. Sacrum is denominator.'),
('11. Amniotic fluid and membrane rupture','Volume, composition, significance, diagnostic role; timely and premature rupture.','Fluid is mostly water with electrolytes, proteins, cells and fetal metabolites. It cushions fetus, permits movement/lung development, avoids cord compression and assists cervical dilation. At term volume is roughly 600-800 mL. PROM is rupture before labor; PPROM is PROM before 37 weeks. Rupture during established labor is timely; rupture before full dilation after labor begins is early. Diagnose by history, sterile speculum pooling, ferning/pH or biochemical tests; ultrasound supports but does not prove rupture. Avoid unnecessary digital examination. Manage by gestation, infection, labor, fetal state and abruption risk.','Meconium can indicate maturity or stress. Foul fluid suggests infection.'),
('12. Fertilization and development','Fertilization and development of conceptus. Embryonic and fetal periods.','Fertilization in the ampulla involves capacitation, acrosome reaction, sperm-oocyte fusion, block to polyspermy and pronuclear fusion to form a diploid zygote. Cleavage forms morula around day 3, blastocyst around days 4-5; implantation begins around days 6-7. Trophoblast forms placenta; embryoblast forms embryo. Germ layers: ectoderm, mesoderm and endoderm. Pre-embryonic period is first 2 weeks; embryonic period weeks 3-8 after fertilization with organogenesis; fetal period begins week 9 and is growth/maturation.','Embryonic weeks 3-8 are the period of greatest structural teratogen risk. Gestational age is counted from LMP, about 2 weeks earlier.'),
('13. Obstetric pelvis','Female pelvis from obstetric viewpoint: greater-pelvis dimensions; planes and dimensions of lesser pelvis; inclination.','True pelvis is the bony birth canal. External measures: interspinous 25-26 cm, intercristal 28-29, intertrochanteric 31-32, external conjugate 20-21. Inlet obstetric conjugate is about 10.5-11 cm and is estimated from diagonal conjugate minus 1.5-2 cm. Planes: inlet; greatest dimensions about 12.5 x 12.5 cm; least dimensions with interspinous diameter 10-10.5 cm; outlet. Pelvic inclination is about 55-60 degrees. Gynecoid pelvis is favorable; android, anthropoid and platypelloid are classical types.','Interspinous diameter is the narrowest fixed transverse diameter. Clinical progress, not pelvimetry alone, diagnoses CPD.'),
('14. Fetal skull as object of labor','Skull bones, sutures, fontanelles, head diameters/circumferences and segments.','Vault bones are frontal, parietal and occipital. Sutures: sagittal, coronal, metopic and lambdoid. Posterior fontanelle is triangular; anterior is diamond-shaped. Well-flexed vertex presents suboccipitobregmatic diameter 9.5 cm and circumference about 32 cm. Occipitofrontal is 11.5 cm; mentovertical in brow is 13.5 cm. Biparietal diameter is 9.5 cm. Small segment equals suboccipitobregmatic, medium equals occipitofrontal, large equals mentovertical. Molding is overlapping of vault bones in labor.','Brow is usually not deliverable at term because mentovertical is the largest AP diameter.'),
('15. Obstetric examination','External obstetric examination. Vaginal examination in labor: indications, technique and interpretation.','External examination includes inspection, fundal height, contractions, fetal heart rate and Leopold maneuvers: fundal pole, lateral back/small parts, presenting part/mobility, and engagement/flexion from pelvic grip. VE requires consent, privacy, asepsis and indication. Assess cervix position/consistency/effacement/dilation, membranes/liquor, presentation, position, station, caput, molding and pelvis. Ischial spines are station 0. In low-risk active labor, routine VE is about every 4 hours, with fewer if not useful. Do not perform digital VE with major antepartum bleeding until previa is excluded.','For cephalic presentation FHR is usually below umbilicus; for breech above it.'),
('16. Physiology and stages of labor','Labor definition, regulation of uterine activity, prodromal period, stages and duration.','Labor is regular uterine activity causing progressive effacement/dilation and birth. Near term, increased prostaglandins, oxytocin receptors and gap junctions, estrogen effects and functional progesterone withdrawal activate myometrium. Fundal dominance, polarity and the triple descending gradient permit coordinated labor. Retraction permanently shortens upper-segment fibers and draws cervix upward. Prodromal changes: lightening, mucus show, irregular contractions and cervical softening. Stages: first, labor to full dilation; second, full dilation to birth; third, birth to placenta; fourth, immediate observation. Duration is variable and must be assessed with progress and wellbeing, not a single clock threshold.','True labor is defined by progressive cervical change, not pain alone.'),
('17. First stage of labor','Course and management of first stage; forces and dilation in primiparas/multiparas.','First stage ends at 10 cm. Latent phase is variable; active labor is commonly considered around 5-6 cm. Primary powers are uterine contractions; secondary powers are maternal bearing-down and mainly act in second stage. In primiparas effacement usually precedes dilation; in multiparas both occur together and first stage is generally shorter. Monitor mother, FHR, contractions, membranes, bleeding, urine/bladder, pain and progress with partograph/Labor Care Guide. Reassess power, passenger and passage if slow. Use augmentation only after excluding obstruction and other causes.','Do not use 1 cm/hour as an absolute requirement. Do not encourage pushing before complete dilation.'),
('18. Second stage and perineal protection','Course and management of second stage. Perineal protection.','Second stage extends from full dilation to birth and has passive descent then active pushing. Confirm full dilation and assess position/station/FHR; prepare neonatal resuscitation and encourage a comfortable birth position. Support spontaneous urge to push; monitor fetal heart and descent. At crowning, communicate to slow/pant, control extension and gently guard perineum. Warm compresses, perineal massage and hands-on support can reduce trauma according to preference. Episiotomy is selective only. Never use routine fundal pressure. Escalate for fetal compromise, no descent, malposition or suspected CPD.','Routine episiotomy and Kristeller maneuver are not recommended.'),
('19. Occiput-anterior mechanism','Biomechanism of labor in anterior occipital presentation.','In LOA vertex, denominator is occiput and leading point is posterior fontanelle. Movements: engagement of biparietal diameter in oblique inlet; descent; increased flexion presenting suboccipitobregmatic diameter; internal rotation bringing occiput under symphysis; extension delivers occiput, bregma, forehead, face and chin; restitution; external rotation with shoulders; delivery of anterior then posterior shoulder and trunk.','Memorize: engagement, descent, flexion, internal rotation, extension, restitution, external rotation, expulsion.'),
('20. Occiput-posterior mechanism','Biomechanism of labor in posterior occipital presentation.','OP often presents with deflexion and back pain. If favorable, descent/flexion is followed by long anterior internal rotation of about 135 degrees, after which delivery proceeds as OA. Persistent OP may deliver face-to-pubis by increased flexion, but has more prolonged labor, trauma and operative delivery. Confirm with VE/ultrasound, monitor progress and FHR, optimize contractions and analgesia. Manual or instrumental rotation requires strict prerequisites and expertise; cesarean for arrest, fetal compromise or disproportion.','OP that rotates anteriorly becomes normal OA delivery. Persistent OP may have prominent anterior fontanelle on VE.'),
('21. Fetal birth trauma','Birth trauma; caput succedaneum; prevention of natal injury.','Birth trauma includes soft tissue injury, cephalohematoma, subgaleal hemorrhage, skull/intracranial injury, nerve palsy, fractures and visceral injury. Risks are macrosomia, prematurity, malpresentation, shoulder dystocia, obstructed/prolonged/precipitate labor and difficult instruments. Caput succedaneum is diffuse pitting scalp edema over presenting part: it crosses sutures, is present at birth and resolves in 24-48 h. Cephalohematoma is subperiosteal and does not cross sutures. Subgaleal hemorrhage spreads widely and can cause shock. Prevent through surveillance, timely cesarean when needed, correct instrument use and skilled breech/shoulder-dystocia management.','Marked caput plus molding and poor descent suggests obstruction.'),
('22. Third stage and placental separation','Course and management of third stage. Methods and signs of placental separation.','Third stage is birth to delivery of placenta, usually under 30 min. Uterine contraction/retraction reduces implantation area, shears placenta from decidua and compresses vessels, the living ligature. Schultze separation begins centrally with fetal surface first; Duncan begins at edge with maternal surface first. Separation signs: firm globular elevated uterus, lengthening cord, small gush, no cord retraction with suprapubic pressure, urge to push. Active management: prophylactic uterotonic, delayed cord clamping when appropriate, controlled traction by trained clinician with countertraction, tone and quantified blood loss assessment. Inspect placenta, membranes, cord and genital tract.','Never pull on the cord before separation: risk is uterine inversion and hemorrhage.'),
('23. Physiological blood loss','Physiological blood loss in childbirth. Methods of determining volume.','Traditional physiological vaginal-birth loss is up to 0.5% maternal body weight, often no more than 400-500 mL. Clinical condition overrides a numerical threshold because pregnancy can mask shock. Quantify objectively: calibrated drape; gravimetric method where 1 g weight gain approximates 1 mL blood; suction volume minus irrigation plus weighed swabs in cesarean birth. Track vitals, urine, Hb/coagulation and shock index HR/SBP. Causes of PPH are 4 Ts: Tone, Trauma, Tissue, Thrombin.','Visual estimation underestimates large loss. Treat the woman, not only the volume.'),
('24. Physiological puerperium','Course and management of normal postpartum period. Prevention of puerperal purulent-septic infection.','Puerperium lasts about 6 weeks. Uterus involutes from umbilicus, descending about one fingerbreadth/day and not palpable abdominally by 10-14 days. Lochia: rubra days 1-3/4, serosa days 4-10, alba thereafter. Monitor bleeding, tone, temperature, wounds, voiding, pain, breasts, mental health and VTE risk. Support feeding, mobility, contraception and warning-sign education. Infection prevention: hand hygiene, asepsis, minimize VE, proper wound care, antibiotic prophylaxis for cesarean, and early treatment of fever, uterine tenderness, foul lochia or wound infection.','Foul lochia, fever or increasing bleeding are abnormal. Ovulation can precede first menstruation.'),
('25. Episiotomy','Perineal incision in labor: indications, postpartum care and complications.','Episiotomy is surgical enlargement of vaginal outlet, performed selectively at crowning with consent, analgesia and asepsis. Mediolateral incision is common and has lower sphincter-extension risk than midline; midline is easier to repair but more likely to extend. Indications: urgent birth for fetal compromise, selected instrumental delivery, rigid scar, selected breech/shoulder dystocia. Repair in layers with absorbable suture after inspecting for extension. Care: analgesia, hygiene, wound checks, stool care and follow-up. Complications: bleeding, hematoma, infection, dehiscence, severe tear, dyspareunia, scar pain and anal incontinence if sphincter injured.','Episiotomy is never routine and cannot replace controlled crowning.'),
]
# 26-64 concise, examination-standard entries
more = [
('26. Vomiting in pregnancy','Classification, clinical features, diagnosis, treatment and tactics.','Nausea/vomiting is common in early pregnancy. Hyperemesis gravidarum is severe vomiting with weight loss, dehydration, ketonuria, electrolyte disturbance or inability to eat/drink. Exclude UTI, GI disease, thyroid disease, hepatitis, neurologic disease and molar/multiple pregnancy. Treat diet modification, antiemetic therapy, thiamine before dextrose in prolonged vomiting, IV fluids/electrolyte correction and admission if severe.','Red flags: abdominal pain, fever, neurologic signs, jaundice, late onset or refractory symptoms.'),
('27. Hypertensive disorders: risk/classification','Edema, proteinuria and hypertensive disorders: risks, ICD-10 classification and pathogenesis.','Categories are chronic hypertension, gestational hypertension, preeclampsia, eclampsia and superimposed preeclampsia. Edema alone is nonspecific. Preeclampsia involves abnormal placentation, antiangiogenic/endothelial dysfunction, vasoconstriction and multisystem injury. Risks: prior preeclampsia, first pregnancy, multifetal gestation, obesity, age extremes, chronic HTN, CKD, diabetes, APS/SLE.','After 20 weeks, new hypertension plus proteinuria or maternal/uteroplacental dysfunction suggests preeclampsia.'),
('28. Hypertensive disorders: diagnosis/treatment','Clinical features, diagnosis, treatment and severity assessment.','Measure BP correctly; evaluate symptoms, urine protein when relevant, CBC/platelets, creatinine, liver enzymes, fetal growth/fluid/Doppler. Severe features include severe-range BP, headache/visual symptoms, pulmonary edema, thrombocytopenia, renal or hepatic dysfunction, RUQ pain and fetal compromise. Stabilize, treat severe BP, use magnesium sulfate when seizure prophylaxis indicated, monitor mother/fetus and plan delivery by gestation/severity.','Proteinuria is not required if new hypertension has end-organ or placental dysfunction.'),
('29. Preeclampsia','Clinical features, diagnosis, treatment and obstetric tactics.','Preeclampsia is hypertension after 20 weeks with proteinuria or maternal organ dysfunction/uteroplacental dysfunction. It may be asymptomatic or cause headache, visual symptoms, epigastric/RUQ pain, dyspnea or reduced movements. Definitive treatment is delivery; balance prematurity against maternal/fetal risk. Use surveillance in stable preterm disease, control severe hypertension, give magnesium sulfate where indicated and corticosteroids if preterm delivery expected.','Do not wait for massive proteinuria if severe features appear.'),
('30. Eclampsia','Definition, pathogenesis, clinical features, diagnosis, emergency care, tactics and complications.','Eclampsia is new generalized seizure or coma in pregnancy/postpartum not explained otherwise, in the setting of preeclampsia. Priorities: call help, left lateral position, protect airway, prevent injury/aspiration, magnesium sulfate protocol, treat severe hypertension, investigate differentials and deliver after maternal stabilization. Complications: stroke, pulmonary edema, renal/liver failure, DIC, abruption, fetal hypoxia and death.','Magnesium sulfate prevents recurrent seizures; delivery follows stabilization, not before it.'),
('31. Abnormal labor','Classification, diagnosis, complications, risk group and prevention.','Includes protraction/arrest, inadequate contractions, tachysystole, discoordination and precipitous labor. Diagnose serially with contractions, cervical change, descent, FHR and assessment of power-passenger-passage. Risks: induction/augmentation, overdistension, malpresentation, CPD, infection, scar. Complications: exhaustion, infection, fetal hypoxia, rupture and PPH. Prevention is risk identification and monitored, rational induction/augmentation.','An arrest diagnosis needs adequate time, assessment and exclusion of CPD.'),
('32. Pathological preliminary period','Diagnosis and management.','Painful irregular contractions before established labor cause fatigue, sleep loss and anxiety without progressive cervical change. Differentiate true labor, abruption, infection, scar problems and malpresentation. Assess mother/fetus, provide rest, hydration, analgesia and appropriate sedation if needed, then reassess. Avoid unjustified oxytocin before true labor and obstruction are excluded.','Key feature: painful ineffective contractions with no cervical progress.'),
('33. Precipitous labor','Clinical picture, complications, management, fetal effect and out-of-hospital birth.','Precipitous labor is unusually rapid birth, often within about 3 hours of onset. Risks include laceration, PPH, abruption, fetal trauma/hypoxia and aspiration. Call assistance, monitor mother/fetus, control delivery rather than pull, prepare neonatal warming/resuscitation and inspect for trauma/hemorrhage. Out-of-hospital: call emergency services, support head, keep newborn warm, do not pull cord/placenta, and transfer urgently.','Rapid labor can be dangerous despite short duration.'),
('34. Uterine inertia','Classification, etiology, diagnosis, treatment and prevention.','Primary inertia is weak contractions from active-labor onset; secondary develops after initially effective labor. Causes include overdistension, exhaustion, analgesia factors, infection, malposition and CPD. Diagnose inadequate contractions with poor progress only after excluding obstruction. Treat reversible causes, bladder, hydration and analgesia; amniotomy/oxytocin only when appropriate and monitored; cesarean for failed progress or compromise.','Never augment suspected obstructed labor.'),
('35. Discoordinated labor','Diagnosis and tactics.','Uncoordinated painful contractions with high tone and poor cervical progress. Exclude abruption, scar rupture, obstruction, malpresentation and oxytocin tachysystole. Stop uterotonics if causing excess activity, provide analgesia, maternal-fetal monitoring and reassess delivery route.','Painful contractions do not necessarily equal effective labor.'),
('36. Contracted pelvis','Anatomically and clinically contracted pelvis: causes, classification, diagnosis and tactics.','Anatomical contraction means reduced bony dimensions from developmental variation, disease, trauma or deformity. Clinical contraction is fetopelvic mismatch demonstrated by labor: poor descent, marked molding/caput, arrest or fetal compromise. Examine pelvis, fetal size/position and labor course. Suspected true CPD generally requires cesarean rather than trial of forceful augmentation.','Clinical contracted pelvis is a labor diagnosis, not a single measurement.'),
('37. Maternal mortality','Definition, rate, causes and risk groups.','Maternal death is death during pregnancy or within 42 days of its termination from pregnancy-related/aggravated causes excluding accidental/incidental causes. Ratio is maternal deaths per 100,000 live births. Direct causes: hemorrhage, hypertensive disease, sepsis, embolism and abortion complications. Indirect causes: cardiac, renal, endocrine and other disease. Prevention: early booking, risk referral, emergency readiness and death review.','Differentiate maternal mortality ratio from rate.'),
('38. First antenatal visit','Scope of examination at first visit and value of early booking.','Take medical, obstetric, surgical, medication, allergy, family, social and mental-health history. Examine BP, BMI/weight, urine and general/obstetric status. Establish gestational age and risk; screen according to local policy for CBC, ABO/Rh/antibodies, infections, urine culture and diabetes risk. Offer dating ultrasound, counseling, vaccines, supplements and referral. Early booking improves dating, prevention and identification of complications.','State that required tests follow national Order No. 1130n and local protocols.'),
('39. Multiple pregnancy','Frequency, diagnosis, placentation and management of pregnancy/birth.','Diagnosis is by ultrasound; determine chorionicity/amnionicity early. Dichorionic-diamniotic has lower risk than monochorionic pregnancies, which risk TTTS, TAPS and selective FGR; monoamniotic twins risk cord entanglement. Risks: prematurity, FGR, anemia, hypertension, malpresentation, hemorrhage. Surveillance and delivery timing depend mainly on chorionicity, complications and presentation.','Chorionicity, not zygosity, is the key management determinant.'),
('40. Pregnancy loss','Classification, etiology, prevention and management of high-risk women.','Pregnancy loss can be sporadic/recurrent and early/late. Causes include fetal chromosomal abnormality, uterine anomaly, APS, endocrine disease, parental genetics and lifestyle; many remain unexplained. Evaluate recurrent loss selectively with uterine assessment, APS testing and other directed tests. Treat cause, optimize chronic disease/lifestyle and give early monitoring/support.','Avoid indiscriminate infection/thrombophilia testing without indication.'),
('41. Spontaneous miscarriage','Classification, etiology, clinical features, diagnosis and treatment.','Types: threatened, inevitable, incomplete, complete, missed and septic miscarriage. Present with bleeding/cramp; use ultrasound and serial hCG when needed to establish viability/location. Options are expectant, medical or uterine evacuation depending on stability, bleeding, infection, gestation and preference. Heavy bleeding, shock or sepsis need urgent resuscitation and evacuation/antibiotics.','Always exclude ectopic pregnancy when location is uncertain.'),
('42. Preterm birth','Classification, clinical features, threatened preterm labor treatment and management.','Birth before 37 completed weeks. It may be spontaneous labor, PPROM or indicated. Assess contractions/cervix, membranes, infection, abruption, fetal condition and gestation. In eligible cases give antenatal corticosteroids, magnesium sulfate for neuroprotection at relevant gestations, short-term tocolysis to gain time, antibiotics for specific indications and transfer to neonatal center. Deliver if infection, abruption, fetal compromise or maternal indication.','Tocolysis is not appropriate in chorioamnionitis, severe preeclampsia/eclampsia, major abruption or fetal death.'),
('43. Post-term pregnancy','Etiology, diagnosis and management.','Post-term is 42+0 weeks; prolonged pregnancy often refers to 41+0. Confirm dating using first-trimester ultrasound. Risks: oligohydramnios, placental insufficiency, meconium, macrosomia, shoulder dystocia and stillbirth. Surveillance and induction are commonly offered by 41 weeks according to protocol; delivery plan reflects cervix, fetal testing and maternal factors.','Incorrect dating is the commonest apparent cause.'),
('44. Intrauterine fetal hypoxia','Classification, diagnosis, preclinical detection, treatment during pregnancy/labor and complications.','Hypoxia can be acute, subacute or chronic and result from placental insufficiency, maternal hypoxemia/anemia, cord compression, abruption, infection or tachysystole. Assess movements, CTG, ultrasound growth/fluid, Dopplers and BPP. Correct reversible causes: maternal position/status, stop uterotonics if tachysystole, treat hypotension; deliver if compromise persists. Outcomes include acidosis, encephalopathy, organ injury and stillbirth.','Chronic placental hypoxia often presents as FGR and abnormal umbilical-artery Doppler.'),
('45. Neonatal asphyxia','Severity assessment, resuscitation and indications for ventilation.','Apgar describes adaptation but does not alone diagnose asphyxia. Initial assessment: term? tone? breathing/crying? Warm, dry, position airway and stimulate. Positive-pressure ventilation is indicated for apnea, gasping or persistent HR below 100/min after initial steps. If HR remains below 60 despite effective ventilation, begin compressions and advanced resuscitation per neonatal protocol.','Effective ventilation is the most important resuscitation action.'),
('46. Diabetes in pregnancy','Course in pregnancy/labor/puerperium, diabetic fetopathy, management and contraindications.','Late pregnancy increases insulin resistance. Maternal risks: preeclampsia, infection, ketoacidosis and operative birth. Fetal risks: anomalies in pregestational diabetes, macrosomia or FGR with vasculopathy, polyhydramnios, stillbirth, neonatal hypoglycemia and respiratory morbidity. Manage preconception glucose, nutrition, monitoring, insulin/medication per protocol, fetal surveillance and delivery planning. Neonate needs glucose monitoring.','Diabetic fetopathy includes macrosomia, cardiomyopathy, hypoglycemia and metabolic adaptation problems.'),
('47. Maternal birth trauma','Perineal, vaginal and cervical tears. Pelvic-joint separation/rupture.','Trauma includes vulvar/perineal/vaginal/cervical tears and pelvic-floor injury. Third- and fourth-degree tears involve anal sphincter and possibly rectal mucosa: identify by systematic inspection, expert repair, antibiotics/bowel care as indicated and follow-up. Cervical tear may cause bleeding with a well-contracted uterus. Symphyseal separation causes severe pelvic pain/impaired walking; manage analgesia, stabilization, physiotherapy and orthopedic input if severe.','In PPH with firm uterus, inspect for genital tract trauma.'),
('48. Chronic hypertension in pregnancy','Course and management; contraindications to continuation.','Chronic hypertension predates pregnancy or appears before 20 weeks. It raises risk of superimposed preeclampsia, abruption, FGR, prematurity, stroke and renal dysfunction. Baseline renal/cardiovascular assessment, safe antihypertensive therapy, aspirin where indicated and serial growth surveillance are key. Severe uncontrolled hypertension or major cardiac/renal/vascular complications require specialist counseling.','Differentiate chronic HTN from gestational HTN by timing and history.'),
('49. Kidney disease and pregnancy','Definition, frequency, predisposing factors, clinical features, diagnosis and treatment.','Includes CKD, glomerular disease, pyelonephritis, AKI and obstruction. Risks increase with reduced GFR, hypertension, proteinuria, diabetes, autoimmune disease and infection. Pregnancy can worsen renal disease and CKD raises preeclampsia, FGR and preterm risk. Monitor BP, creatinine, proteinuria, urine culture where indicated, fetal growth and medication safety. Joint obstetric-nephrology care is required.','Serum creatinine normally falls in pregnancy; a rise is important.'),
('50. Heart disease in pregnancy','Course and management of pregnancy with heart defects; contraindications.','Pregnancy raises blood volume and cardiac output, stressing structural disease. Highest risk: pulmonary arterial hypertension, severe ventricular dysfunction, severe stenotic valve disease, major aortopathy and unstable arrhythmia. Use preconception risk assessment, multidisciplinary cardio-obstetric care, safe medication review, thrombosis prevention when indicated and individualized delivery plan. Vaginal birth is often preferred unless cardiac/obstetric indication for cesarean.','Pulmonary hypertension is among the highest-risk conditions for maternal death.'),
('51. Bleeding in pregnancy','Etiology, classification, risk group and prevention.','Early bleeding: miscarriage, ectopic, cervical lesion, subchorionic hemorrhage. Late bleeding: placenta previa, abruption, vasa previa, labor-related bleeding and rupture. First priorities are maternal ABCs, IV access, blood group/crossmatch and fetal assessment when viable. Ultrasound locates placenta. Avoid digital VE in significant late bleeding until placenta previa is excluded. Prevention includes risk management and prior-cesarean/accreta surveillance.','Painful bleeding suggests abruption; painless bright bleeding suggests previa, but exceptions occur.'),
('52. Placental abruption','Premature separation of normally implanted placenta: definition, etiology, diagnosis, tactics and complications.','Abruption is placental separation after 20 weeks before birth. Risks: hypertension, trauma, smoking/cocaine, prior abruption, PPROM. Features: painful bleeding, tender hypertonic uterus, contractions, shock and fetal distress; blood may be concealed. Diagnosis is clinical; ultrasound can miss it. Resuscitate, obtain blood/coagulation tests, monitor continuously, correct coagulopathy and expedite delivery for severe maternal/fetal compromise.','DIC is a major complication, particularly with concealed severe abruption.'),
('53. Placenta previa','Definition, etiology, classification, diagnosis and tactics.','Placenta previa is low-lying placenta covering or close to internal os late in pregnancy. Classic presentation is painless bright-red bleeding. Risks include prior cesarean/uterine surgery, ART, multiparity, smoking and multiple gestation. Transvaginal ultrasound accurately defines placental edge and can assess accreta risk. Manage bleeding, anemia, gestation and fetal status; major previa usually requires cesarean.','Never perform a digital VE with suspected previa.'),
('54. Early postpartum hemorrhage','Etiology, diagnosis, tactics and sequence for hypotonic bleeding.','PPH is excessive bleeding after birth causing risk of instability. Use 4 Ts: Tone, Trauma, Tissue, Thrombin. Immediate bundle: call help, quantify loss, ABC/resuscitation, uterine massage, two large IV lines, blood products/labs, uterotonics and tranexamic acid per protocol, empty bladder, identify cause. For atony escalate to bimanual compression, balloon tamponade, arterial/surgical measures and hysterectomy if life-saving.','Do simultaneous resuscitation and hemorrhage control. Do not wait for hypotension.'),
('55. Obstetric DIC','Etiology, pathogenesis, clinical/laboratory stages, treatment and prevention.','DIC is systemic coagulation activation causing microthrombi, consumption of factors/platelets and bleeding. Triggers: abruption, AFE, sepsis, severe preeclampsia/HELLP, massive hemorrhage, retained dead fetus. Findings: bleeding, thrombocytopenia, prolonged PT/aPTT, low fibrinogen, high D-dimer. Treat cause and replace RBCs, plasma, platelets and fibrinogen guided by bleeding/labs, with critical care support.','In obstetrics, falling fibrinogen is particularly alarming.'),
('56. Hemorrhagic shock','Etiology, pathogenesis, clinical stages and obstetric tactics.','Acute blood loss reduces preload, cardiac output and oxygen delivery, causing tachycardia, vasoconstriction, oliguria, acidosis, hypotension and organ failure. Causes include ectopic, miscarriage, abruption, previa/accreta, rupture and PPH. Activate massive hemorrhage response, control source, warm patient, obtain rapid blood products, monitor urine/lactate/coagulation and perform definitive surgery/intervention.','Tachycardia and rising shock index can precede hypotension.'),
('57. Uterine rupture','Classification, etiopathogenesis, clinical features, diagnosis, tactics and surgical extent.','Rupture is complete or incomplete, scarred or unscarred, spontaneous or traumatic. Risks: prior uterine incision, obstructed labor, excessive uterotonics, trauma and prior myomectomy. Signs: acute pain, abnormal FHR, loss of station, bleeding, altered contractions and shock. It is an immediate laparotomy emergency: deliver fetus, control hemorrhage, repair if feasible or hysterectomy for uncontrolled bleeding/extensive injury.','Fetal bradycardia is often the earliest sign in scar rupture.'),
('58. Postpartum purulent-septic diseases','Definition/classification; postpartum ulcer etiology, diagnosis and treatment sequence.','Postpartum infections range from perineal/wound infection and endometritis to pelvic cellulitis, thrombophlebitis, peritonitis and sepsis. Postpartum ulcer is infected perineal/vaginal/cervical wound, often polymicrobial. Evaluate systemic illness, inspect wound, culture when useful, give analgesia and severity-appropriate antibiotics, drain/debride if needed and monitor for spread.','Risk increases with prolonged rupture/labor, trauma, hemorrhage and cesarean.'),
('59. Postpartum endometritis and spread','Frequency, etiology, diagnosis and treatment of endometritis, metroendometritis, thrombophlebitis and parametritis.','Endometritis is polymicrobial ascending uterine infection, commoner after cesarean, prolonged ROM/labor, retained tissue and repeated VE. Fever, uterine tenderness, foul lochia and tachycardia are typical. Give broad-spectrum IV antibiotics and assess retained products, abscess or wound infection. Persistent fever despite antibiotics suggests septic pelvic thrombophlebitis or abscess. Parametritis is spread into parametrial tissue.','Postpartum fever needs a broad differential: wound, breast, urine, lung and thrombosis.'),
('60. Pelvic peritonitis and post-cesarean peritonitis','Mechanisms, risk group, clinical features, diagnosis, tactics and prevention.','Spread may occur from endometritis, uterine incision, bowel/urinary injury or abscess. Risks: chorioamnionitis, prolonged ROM, emergency cesarean, obesity, diabetes and hemorrhage. Features: fever, tachycardia, pain/distension, guarding, ileus and sepsis. Resuscitate, give broad-spectrum antibiotics, image if stable, and achieve urgent source control by drainage/reoperation when required.','Sepsis plus peritoneal signs after cesarean is a source-control emergency.'),
('61. Infectious-toxic shock','Definition, frequency, maternal mortality role, pathogenesis, clinical features, diagnosis, complications and treatment.','Septic/toxic shock is infection-associated circulatory and cellular/metabolic dysfunction causing hypotension and organ failure. It may be polymicrobial postpartum or toxin-mediated staphylococcal/streptococcal disease. Recognize fever/hypothermia, tachycardia, hypotension, altered mentation, lactate rise, coagulopathy and renal failure. Obtain cultures without delaying broad antibiotics, resuscitate, start vasopressors if required and urgently remove/drain source.','Antibiotics and source control should not wait for culture results.'),
('62. Obstetric sepsis','Role in maternal mortality, etiopathogenesis, clinical features, diagnosis, treatment, infusion and antibiotics.','Obstetric sepsis is infection with life-threatening organ dysfunction during pregnancy, birth, abortion or puerperium. Sources: uterus, wound, urinary tract, lungs, breast and bloodstream. Recognize abnormal vital signs, altered mental state, oliguria, lactate and fetal compromise. Give timely broad-spectrum IV antibiotics, cultures where feasible, balanced fluids tailored to response, vasopressors for persistent hypotension and urgent source control. Tailor/de-escalate antibiotics to cultures.','Avoid fluid overload, especially with preeclampsia or cardiac/renal disease.'),
('63. Lactational mastitis','Classification, clinical features, maternity-hospital tactics, breastfeeding decision, suppression indications and prevention.','Spectrum: milk stasis/inflammatory mastitis, bacterial mastitis and abscess. Painful focal erythema, fever and flu-like symptoms are typical. Continue breastfeeding or effective milk expression in most cases; correct latch/drainage, give analgesia and antibiotics when bacterial disease likely. Ultrasound for possible abscess, which requires drainage. Suppression is reserved for specific clinical contraindications or informed choice. Prevent with feeding support and avoidance of nipple trauma/engorgement.','Breastfeeding is usually safe and helps drainage, even with mastitis.'),
('64. Rh isoimmunization','Maternal-fetal Rh incompatibility: etiopathogenesis, sensitization routes, prevention and management.','RhD-negative woman exposed to RhD-positive fetal cells can form anti-D. In later antigen-positive pregnancy, IgG crosses placenta causing fetal anemia/HDFN. Sensitizing events include delivery, miscarriage, bleeding, trauma, procedures, ECV and transfusion. Prevent with anti-D immunoglobulin in unsensitized women after sensitizing events and scheduled prophylaxis by local protocol. Once sensitized, identify antibody/fetal antigen, follow titers and MCA Doppler, and refer for intrauterine transfusion/delivery planning.','Anti-D prophylaxis must be recorded after every sensitizing event; it is ineffective once immune anti-D is present.'),
]
Q.extend(more)
assert len(Q)==64, len(Q)
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canvas.setFont('Helvetica',8); canvas.setFillColor(HexColor('#5F6E7B')); canvas.drawString(1.6*cm,1.0*cm,'Obstetrics Oral-Exam Guide | Questions 1-64')
canvas.drawRightString(19.4*cm,1.0*cm,f'Page {doc.page}')
canvas.restoreState()
doc=SimpleDocTemplate(OUT,pagesize=A4,rightMargin=1.6*cm,leftMargin=1.6*cm,topMargin=1.6*cm,bottomMargin=1.8*cm,title='Obstetrics Questions 1-64 Oral-Exam Guide',author='Orris')
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story += [Spacer(1,2.2*cm), Paragraph('OBSTETRICS',styles['CoverTitle']), Paragraph('Questions 1-64',styles['CoverTitle']), Paragraph('Concise Oral-Exam Answer Guide',styles['CoverSub']), Spacer(1,.6*cm), Paragraph('English translation of the Russian examination topics with structured, exam-focused answers.',styles['CoverSub']), Spacer(1,1.2*cm), Paragraph('<b>How to use this guide</b><br/>Start every oral answer with a definition. Then use the headings embedded in each answer: classification/etiology, clinical features and diagnosis, management, complications, and examiner points. Medication doses, operative details, and delivery decisions must follow local protocol and direct clinical supervision.',styles['Bodyx']), Spacer(1,.5*cm), Paragraph('Educational material only. It is not a substitute for hospital protocols or specialist supervision in obstetric emergencies.',styles['Exam']), PageBreak()]
story.append(Paragraph('Contents',styles['H1x']))
for start,end,name in [(1,10,'Normal pregnancy, fetus, placenta and presentation'),(11,20,'Amniotic fluid, pelvis, examination and normal labor'),(21,30,'Birth trauma, puerperium and hypertensive disorders'),(31,40,'Abnormal labor, antenatal care and pregnancy loss'),(41,50,'Preterm/post-term birth, fetal condition and maternal disease'),(51,64,'Hemorrhage, sepsis and Rh disease')]:
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story.append(PageBreak())
for i,(title,translation,answer,points) in enumerate(Q,1):
if i in [1,11,21,31,41,51]:
section={1:'Section I. Foundations and normal pregnancy',11:'Section II. Fetus, pelvis and normal labor',21:'Section III. Puerperium and hypertensive disorders',31:'Section IV. Abnormal labor and high-risk pregnancy',41:'Section V. Preterm birth, fetal condition and maternal disease',51:'Section VI. Hemorrhage, infection and alloimmunization'}[i]
story.append(Paragraph(section,styles['H1x']))
story.append(Paragraph(title,styles['H2x']))
story.append(Paragraph(f'<b>Question translation:</b> {escape(translation)}',styles['Small']))
story.append(Paragraph(answer,styles['Bodyx']))
story.append(Paragraph(f'<b>Examiner points:</b> {escape(points)}',styles['Exam']))
story.append(PageBreak()); story.append(Paragraph('Final rapid-revision checklist',styles['H1x']))
check=['Perinatal mortality: late fetal deaths plus early neonatal deaths per 1,000 total births.','Fertilization occurs in ampulla; organogenesis is weeks 3-8 after fertilization.','Smallest vertex diameter: suboccipitobregmatic 9.5 cm.','True labor means progressive cervical change.','4 Ts of postpartum hemorrhage: Tone, Trauma, Tissue, Thrombin.','Preeclampsia: hypertension after 20 weeks plus proteinuria or maternal/uteroplacental dysfunction.','Eclampsia: stabilize first, magnesium sulfate, then delivery as indicated.','Never perform digital vaginal examination with suspected placenta previa.','Abruption is usually painful; previa is classically painless.','Obstetric sepsis requires immediate antibiotics, resuscitation and source control.','Rh prevention: anti-D for unsensitized RhD-negative women after relevant sensitizing events.']
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story.append(Spacer(1,.4*cm)); story.append(Paragraph('Evidence note: the guide uses general contemporary obstetric principles. For current Russian requirements, follow Ministry of Health Order No. 1130n and the local maternity-hospital emergency protocols. Current WHO guidance supports objective postpartum blood-loss measurement, use of a prophylactic uterotonic in third stage, and structured first-response treatment for postpartum hemorrhage.',styles['Small']))
doc.build(story,onFirstPage=header,onLaterPages=header)
print(OUT)
python3 "/tmp/workspace/obstetrics-oral-exam-pdf/src/create_pdf.py" && python3 -c "from pypdf import PdfReader; p='/tmp/workspace/obstetrics-oral-exam-pdf/output/Obstetrics_Questions_1-64_Oral_Exam_Guide.pdf'; r=PdfReader(p); print('pages',len(r.pages),'size',__import__('os').path.getsize(p)); print(r.pages[0].extract_text()[:500]); print(r.pages[-1].extract_text()[:500])"
python3 -c "from pypdf import PdfReader; p='/tmp/workspace/obstetrics-oral-exam-pdf/output/Obstetrics_Questions_1-64_Oral_Exam_Guide.pdf'; t='\n'.join(x.extract_text() or '' for x in PdfReader(p).pages); required=['1. Organization of obstetric care','25. Episiotomy','26. Vomiting in pregnancy','50. Heart disease in pregnancy','64. Rh isoimmunization','Final rapid-revision checklist']; missing=[x for x in required if x not in t]; print('chars',len(t),'missing',missing); print('question_titles',sum(1 for i in range(1,65) if ('%d. '%i) in t))"
Obstetrics Questions 1 64 Oral Exam Guide
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Give me answers from 26 - 30