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Obstetrics & Gynaecology

Maternal-fetal medicine, obstetrical complications, gynecologic oncology, and reproductive care.

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Q2(h). Medical management of endometriosis. (10 Marks)

description Clinical Response
Short Answer Q2(h) — 10 MARKS
Medical Management of Endometriosis
Agent ClassDetails
NSAIDsFirst-line symptomatic analgesia for dysmenorrhoea; does not treat underlying disease progression
Combined oral contraceptivesFirst-line hormonal therapy — continuous or cyclical use suppresses ovulation and reduces menstrual flow, providing symptomatic relief with a favourable long-term safety profile
Progestins (oral, depot, or LNG-IUS)Effective alternative/adjunct — induce endometrial decidualisation and atrophy of ectopic implants; LNG-IUS particularly useful for associated heavy menstrual bleeding
GnRH agonists (e.g., leuprolide)Induce a hypoestrogenic “medical menopause” state, effective for pain control; use limited by hypoestrogenic side effects (bone density loss, vasomotor symptoms) unless combined with “add-back” hormone therapy
GnRH antagonists (e.g., elagolix, relugolix combinations)Newer oral agents providing more rapid, dose-dependent oestrogen suppression without the initial flare effect of agonists; increasingly used with built-in low-dose hormonal add-back to balance efficacy and bone/vasomotor side effects
Aromatase inhibitorsAdjunctive option in refractory cases, particularly where extra-ovarian oestrogen production (from ectopic implants themselves) contributes to persistent symptoms despite ovarian suppression
Clinical Pearl
Medical therapy for endometriosis treats symptoms (primarily pain) by suppressing the hormonal drive to ectopic implants — it does not eliminate existing lesions or adhesions, so symptoms typically recur once therapy is stopped, and medical therapy does not reliably improve fertility (surgery remains the mainstay for endometriosis-associated infertility).
Consolidated References
  1. Nicolaides KH. Screening for fetal aneuploidies at 11 to 13 weeks. Prenat Diagn. 2011.
  2. Wald NJ, et al. Antenatal maternal serum screening for Down’s syndrome — quadruple test performance data. J Med Screen.
  3. Rolnik DL, et al. Aspirin versus placebo in pregnancies at high risk for preterm pre-eclampsia (ASPRE trial). N Engl J Med. 2017.
  4. FIGO Working Group on Good Clinical Practice in Maternal-Fetal Medicine. Best practice for first-trimester risk assessment and pre-eclampsia prevention.
  5. Assisted Reproductive Technology (Regulation) Act, 2021, and Rules, Government of India.
  6. ACR-SPR / ACOG practice guidance on MRI use in pregnancy.
  7. Practice Committee of the American Society for Reproductive Medicine. Mature oocyte cryopreservation — a guideline. Fertil Steril.
  8. ERAS Society. Enhanced Recovery After Surgery guidelines for gynaecologic/oncologic surgery and caesarean delivery.
  9. Ministry of Health and Family Welfare, Government of India. Surakshit Matritva Aashwasan (SUMAN) guidelines.
  10. Harlow SD, et al. Executive summary of the Stages of Reproductive Aging Workshop + 10 (STRAW+10). Menopause. 2012.
  11. Advincula AP, et al. Role of robotic surgery in benign and oncologic gynaecology — review. Obstet Gynecol Clin North Am.
  12. Johnson NP, et al. ESHRE Guideline: management of women with endometriosis (medical therapy section). Hum Reprod.
Model Answer Key — Obstetrics & Gynaecology Paper IV, MPMSU Jabalpur (June 2023) | For academic study purposes
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Q11. Kawasaki Disease (KD) & Coronary Aneurysms

description Clinical Response
Q141 ★ · DNB/MD 2025/1
Kawasaki Disease (KD) & Coronary Aneurysms
Examiner's Intent: KD is a near-universal, guaranteed high-yield topic given both its clinical importance and its direct comparative relationship to MIS-C (Section 3, Q47) — examiners expect precise AHA diagnostic criteria (complete versus incomplete), a clear understanding of the echocardiographic coronary surveillance schedule, and knowledge of the IVIG-resistance management escalation pathway.

AHA Guidelines — Complete Kawasaki Disease

Diagnosed based on fever for ≥5 days combined with at least 4 of the following 5 principal clinical features:

#FeatureDetails
1Bilateral, non-exudative conjunctival injection
2Oral mucosal changesErythematous, cracked lips; “strawberry tongue” (prominent erythematous papillae); diffuse oral/pharyngeal erythema
3Polymorphous rashVariable in morphology, typically truncal
4Extremity changesAcute: erythema/edema of hands and feet. Subacute (2–3 weeks): periungual desquamation — a useful retrospective clue
5Cervical lymphadenopathyTypically unilateral, ≥1 node ≥1.5 cm — the least consistently present feature

Incomplete Kawasaki Disease

In a child with fever ≥5 days and only 2–3 principal criteria (particularly relevant in infants, who carry disproportionately elevated coronary complication risk), the AHA algorithm incorporates:

  • Supplemental laboratory criteria — elevated CRP/ESR plus supportive findings: anemia, thrombocytosis after day 7, hypoalbuminemia, elevated ALT, leukocytosis, sterile pyuria
  • Echocardiographic findings — coronary artery abnormalities are themselves sufficient supportive evidence to diagnose incomplete KD and initiate treatment

[Diagram: AHA incomplete-KD algorithm flowchart: fever ≥5 days + 2-3 criteria → CRP/ESR → supplemental labs / echo → diagnosis pathway]

Echocardiographic Screening for Coronary Artery Aneurysms

TimingPurpose
At diagnosisBaseline assessment
~1–2 weeks after treatment initiationEarly surveillance
~4–6 weeks after illness onsetLater surveillance (extended further if coronary abnormalities confirmed)

Coronary findings are graded using standardized z-score-based (body-surface-area-adjusted) classification: no involvement → small → medium → large/giant aneurysm — directly determining follow-up intensity and antithrombotic strategy.

IVIG Resistance and Escalation Therapy

Standard initial treatment: IVIG 2 g/kg single infusion + aspirin.

  1. Second dose of IVIG (2 g/kg) — first escalation step for IVIG-resistant disease
  2. Methylprednisolone/corticosteroids — escalation step, or upfront in high-risk children (validated risk-scoring systems)
  3. Infliximab (anti-TNF-alpha) — for refractory disease despite IVIG + steroid escalation

Long-Term Management

Stratified by aneurysm size: low-dose aspirin alone for small aneurysms → combined antiplatelet + anticoagulant therapy for large/giant aneurysms (elevated thrombosis risk), with periodic cardiology follow-up, stress testing, and consideration of interventional/surgical revascularization for significant coronary stenosis.

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