What is new in post partum Haemorrage

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"postpartum hemorrhage" management

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new updates postpartum hemorrhage management guidelines 2024 2025

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https://www.ncbi.nlm.nih.gov/books/NBK619233

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PMID: 40237648

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PMID: 40743526

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PMID: 41056961

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What's New in Postpartum Haemorrhage (PPH) - 2025 Updates

Major Development: WHO Consolidated Guidelines (October 2025)

The WHO, FIGO, and International Confederation of Midwives released the first-ever consolidated guidelines specifically focused on PPH on October 5, 2025, launched at the FIGO World Congress in Cape Town. These include 51 recommendations (20 new or updated; 31 revalidated) across prevention, diagnosis, treatment, supportive care, and health systems.

1. Revised Definition of PPH

The threshold is no longer a simple volume-only rule. The new preferred definition is:
Blood loss ≥ 1,000 mL accompanied by signs of hypovolemia (rather than the older ≥500 mL cutoff)
A major Lancet meta-analysis by Gallos et al. (2025) of 312,151 women across 23 countries (PMID: 41056961) found that:
  • The conventional 500 mL threshold has only 75.7% sensitivity for predicting mortality or severe morbidity
  • Sensitivity improves to 87-88% when combining blood loss of 300-450 mL plus any abnormal haemodynamic sign (pulse >100, SBP <100, DBP <60, or shock index >1.0)
  • This supports a combined clinical marker approach over volume alone for earlier diagnosis

2. New Guidance on Tranexamic Acid (TXA) - KEY UPDATE

Two new WHO recommendations (2025):
  • Rec. 14 (NEW): TXA is NOT recommended for prevention of PPH at vaginal birth
  • Rec. 15 (NEW): TXA is NOT recommended for prevention of PPH at caesarean birth
This is a significant shift - TXA remains recommended for treatment of established PPH, but prophylactic use is no longer supported. The Cochrane meta-analysis by Cheema et al. (2023) on TXA for prevention at C-section confirms lack of benefit to justify prophylactic use.

3. Uterotonic Rankings - Updated Cochrane Network Meta-Analysis (2025)

The landmark Cochrane network meta-analysis by Gallos et al. (2025) (PMID: 40237648) covering 122 trials, 121,931 women across 48 countries found:
RankAgentPPH ≥500 mL vs Oxytocin
1st (tied)Ergometrine + OxytocinRR 0.76 (high certainty)
1st (tied)Misoprostol + OxytocinRR 0.70 (moderate certainty)
EquivalentCarbetocinSimilar (high certainty)
  • Combination agents outperform oxytocin alone, though with more side effects
  • WHO still recommends oxytocin 10 IU (IM/IV) as the first-line standard (Rec. 24, revalidated), but combination therapy is preferred where feasible
  • Carbetocin (heat-stable formulation) continues to be supported especially in low-resource settings without cold chains

4. Updated Diagnostic Approach

  • Universal objective blood loss measurement (calibrated drapes, weighing) is now recommended - not visual estimation
  • Standardized risk assessment tool before and after every delivery
  • Early action at combined threshold of ≥300 mL + any haemodynamic sign, rather than waiting for 500 mL

5. ACOG Update: Nonsurgical Hemorrhage-Control Devices (October 2025)

ACOG released a focused Clinical Practice Update (PMID: 40743526) revising guidance on intrauterine balloon tamponade and other nonsurgical devices, updating Practice Bulletin 183 (2017). Key points include:
  • Uterine balloon tamponade remains a core second-line intervention
  • Newer devices (e.g. Jada system - intrauterine vacuum-induced hemorrhage control) are now addressed with revised guidance
  • Devices should be used as part of a structured bundle, not in isolation

6. Structured Treatment Bundle (Revalidated & Reinforced)

The first-response care bundle (Rec. 29, revalidated) for all vaginal births includes:
  1. Objective assessment of blood loss
  2. Rapid uterine massage
  3. Uterotonic agent (oxytocin IV/IM)
  4. Tranexamic acid 1g IV (for treatment, within 3 hours of delivery)
  5. IV fluids
  6. Genital tract examination
  7. Clear escalation to second-line (balloon tamponade → surgical repair → embolization → hysterectomy)

7. Aetiology Confirmed by Global Data

The Lancet meta-analysis confirmed the relative proportions:
  • Uterine atony: 70.6% of cases
  • Genital tract trauma: 16.9%
  • Retained placenta: 16.4%
  • Coagulation disorders: less common
This reinforces targeting atony prevention as the primary strategy.

8. Health Systems & Global Implementation

The 2025 WHO guidelines place major emphasis on:
  • Supply chain strengthening for heat-stable uterotonics in low-resource settings
  • Training modules and simulation-based emergency drills for frontline workers
  • National implementation guides, developed with UNFPA
  • Equity lens - most of the 70,000 annual deaths occur in low- and middle-income countries

Summary Table: What Changed in 2025

AreaOld GuidanceNew/Updated 2025
Definition≥500 mL≥1,000 mL with haemodynamic signs OR ≥300-450 mL + abnormal vitals
TXA prophylaxisDebated/used by someNOT recommended (vaginal or C-section)
TXA treatmentRecommendedConfirmed - within 3 hours
Best uterotonicOxytocin aloneOxytocin + ergometrine OR oxytocin + misoprostol superior
Diagnosis thresholdVolume-onlyVolume + haemodynamic signs combined
Nonsurgical devicesACOG 2017 guidanceUpdated 2025 (includes Jada system)

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Massive transfusion b protocol what is it

The Massive Transfusion Protocol (MTP) is a pre-activated, coordinated system for rapidly delivering large volumes of blood products in a fixed ratio to patients with life-threatening hemorrhage. It aims to prevent the "lethal triad" of coagulopathy, hypothermia, and acidosis by replacing blood components in a balanced ratio rather than just giving packed red cells.
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"massive transfusion protocol" hemorrhage ratio

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massive transfusion protocol MTP blood product ratios 1:1:1 definition activation criteria 2024 2025

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Massive Transfusion Protocol (MTP) - Complete Overview

What Is It?

A Massive Transfusion Protocol (MTP) is a pre-activated, institutional, multidisciplinary algorithm that coordinates the rapid delivery of blood products in fixed ratios to patients with life-threatening hemorrhage. It exists because massive blood loss involves more than just red cell loss - it depletes clotting factors, fibrinogen, and platelets simultaneously, making ratio-based replacement superior to packing red cells alone.
  • Rosen's Emergency Medicine, p. 2429
  • Henry's Clinical Diagnosis, p. 881

Definition of Massive Transfusion (Trigger Volume)

SettingDefinition
Adults> 10 units PRBCs in 24 hours OR ≥3 units in 1 hour OR ≥150 mL/min blood loss
Adults (volume)Loss of 1 complete blood volume (~5L/70 mL/kg) in 24h
Children≥80 mL/kg in 24h OR ≥40 mL/kg in 3 hours
These volume-based definitions have limited real-world utility because transfusion must often begin before such thresholds are reached.

Activation Criteria - The ABC Score

The Assessment of Blood Consumption (ABC) Score is the most commonly used validated trigger. Activate MTP if 2 or more of the following are present:
CriterionScore
Penetrating mechanism1
SBP ≤ 90 mmHg1
Heart rate > 120 bpm1
Positive FAST exam1
ABC score ≥ 2 = Activate MTP
Other activation triggers used clinically:
  • Blood loss > 150 mL/min
  • Blood loss > 50% of blood volume within 3 hours
  • Anticipated need for ≥3 units in 1 hour

The Core Concept: Damage Control Resuscitation (DCR)

MTP is the clinical implementation of Damage Control Resuscitation, which arose from military experience in Iraq and Afghanistan. The rationale:
  1. Massive hemorrhage depletes all blood components - red cells, plasma, platelets, and clotting factors
  2. Replacing only red cells (old strategy) worsens the lethal triad: coagulopathy + hypothermia + acidosis
  3. Reconstituting whole blood by giving components in a ratio approximating whole blood is the solution

The 1:1:1 Ratio - The Standard of Care

The landmark PROPPR trial (Pragmatic Randomized Optimal Platelet and Plasma Ratios) compared:
Ratio (PRBCs : FFP : Platelets)Outcome
1:1:1Fewer deaths from exsanguination at 24h
2:1:1No difference in overall 30-day mortality
The 1:1:1 ratio is now the standard in most MTPs, despite no difference in 30-day mortality - the reduction in exsanguination death at 24h is the key benefit.
  • Rosen's Emergency Medicine, p. 2430
  • Bailey & Love's Surgery, 28th Ed.

MTP Protocol - Step-by-Step (Denver Health/Schwartz's Surgery Model)

Here is the MTP flowchart from Schwartz's Principles of Surgery:
Denver Health MTP Flowchart - Schwartz's Surgery
Figure 7-33 from Schwartz's Principles of Surgery 11th Ed - Denver Health Medical Center MTP

Phase 1 - Trigger & Activate

  • SBP ≤70 OR (SBP 71-90 AND HR ≥108) PLUS any of: penetrating torso injury / major pelvic fracture / FAST+ in >1 region
  • ACTIVATE MTP - call blood bank, notify OR, anaesthesia, lab
  • Give CaCl₂ 1g IV immediately (combat citrate-induced hypocalcaemia)

Phase 2 - Empiric (Pre-Lab) Transfusion

ShipmentPRBCsFFPPlateletsCryo
Pack 14 units2 units--
Pack 24 units2 units1 unit10 units
Simultaneously: correct hypothermia, correct acidosis, normalize Ca²⁺, haemorrhage control

Phase 3 - Goal-Directed (TEG/ROTEM-Guided)

Once a Citrated Rapid TEG result is available, replace components based on specific deficits:
TEG ParameterThresholdGive
ACT (clotting time)> 128 secFFP 2 units
Angle (fibrin kinetics)< 65°Cryoprecipitate 10 units
MA (platelet function)< 55 mmPlatelets 1 unit (apheresis)
LY30 (fibrinolysis)≥ 10%TXA 1g
If TEG is unavailable, use conventional coagulation triggers:
  • PT/PTT > 1.5x control → FFP 2 units
  • Platelets < 50,000/µL → 1 unit apheresis platelets
  • Fibrinogen < 100 mg/dL → 10 units pooled cryoprecipitate

The "Lethal Triad" MTP Targets

         COAGULOPATHY
              △
             /|\
            / | \
           /  |  \
    ACIDOSIS──────HYPOTHERMIA
MTP directly counteracts all three limbs by:
  • Clotting factors/FFP → treat coagulopathy
  • Warming all blood products → prevent/treat hypothermia
  • Restoring perfusion (not crystalloid overload) → treat acidosis

Blood Products in MTP - At a Glance

ProductRoleKey Points
PRBCsOxygen-carrying capacityStart with Group O uncrossmatched if urgent; Rh-negative preferred for females of childbearing age
FFP (Fresh Frozen Plasma)Replaces all clotting factorsGiven when PT/APTT >1.5x normal
PlateletsHaemostatic plugGive if count <50,000; use apheresis units
CryoprecipitateFibrinogen + Factor VIII + vWF + XIIIGive if fibrinogen <100 mg/dL
Whole Blood (Low-Titer Type O)All components in one unitRe-emerging as preferred option especially in pre-hospital/military settings
Tranexamic Acid (TXA)Antifibrinolytic1g IV within 3 hours of injury/bleeding onset; do NOT give after 3 hours
CalciumReverses citrate toxicityGive CaCl₂ or calcium gluconate with every pack

Whole Blood - The Emerging Trend

Low-Titer Group O Whole Blood (LTOWB) is regaining favour, especially in trauma and military settings:
  • Provides all components in physiological ratios in a single unit
  • Reduces logistical burden in pre-hospital care
  • Reduces donor exposures
  • ACS TQIP now includes guidance on LTOWB in MTP frameworks

When to Stop (MTP Termination Criteria)

  • Bleeding is controlled surgically
  • Haemodynamics are stable
  • Labs normalize (Hb, PT/INR, fibrinogen, platelets in acceptable range)
  • Clinical decision by senior physician

Complications of Massive Transfusion

ComplicationMechanismManagement
HypothermiaCold blood productsFluid warmers, warm blankets, Bair Hugger
HypocalcaemiaCitrate chelates calciumCaCl₂ 1g IV per pack
HyperkalaemiaStored blood releases K⁺Monitor, ECG
Metabolic acidosisHypoperfusion + citrateOptimize O₂ delivery; NOT bicarbonate
TRALIImmune reaction to donor plasmaSupportive; use male donor or pathogen-reduced plasma
Dilutional coagulopathyVolume replacing coagulation factorsGuided by TEG/ROTEM
Hypothermic coagulopathyCold reduces clotting factor activityWarming

Key Evidence Base

  • The PROPPR trial (Holcomb et al.): 1:1:1 reduces exsanguination deaths at 24h vs 2:1:1
  • Williams et al., Cochrane 2025 - transfusion of blood products for PPH management (PMID: 39911088)
  • ACS TQIP MTP Guidelines - standardization across trauma systems, 2025
  • TEG/ROTEM-guided resuscitation associated with lower mortality vs conventional coag parameters in trauma (Rosen's EM, p. 2430)

Bottom line: MTP is not just "give lots of blood" - it is a structured, ratio-driven, goal-directed protocol that reconstructs whole blood from components, fights the lethal triad, and is triggered early using validated criteria (ABC score ≥2). The 1:1:1 ratio of PRBCs:FFP:platelets is the current standard, with TEG/ROTEM enabling personalised correction once labs are available.

What is new in Endomeetriosis

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Endometriosis is a chronic gynaecological condition where endometrial-like tissue grows outside the uterus, causing pain, infertility and inflammation. Recent years have seen major advances in non-invasive diagnosis, new drug approvals, and better understanding of its pathogenesis.
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endometriosis diagnosis treatment guidelines

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endometriosis new developments 2024 2025 diagnosis biomarkers treatment guidelines

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PMID: 38555044

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PMID: 39488350

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PMID: 40312882

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https://www.emjreviews.com/reproductive-health/congress-revi…

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endometriosis linzagolix elagolix relugolix new drug treatment 2024 2025

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endometriosis 2025 new drugs GnRH antagonist linzagolix ACOG clinical diagnosis laparoscopy not required

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What's New in Endometriosis - 2024/2025 Updates

Quick Pathogenesis Recap

Endometriosis pathogenesis - retrograde menstruation, implant survival via aromatase, PGE2, angiogenic factors
Fig. 17.9 from Robbins & Kumar Basic Pathology - Endometriotic implants survive through aromatase-driven estrogen production, PGE2, COX-2-activated macrophages, and angiogenic factors
Endometriosis affects 5-10% of reproductive-age women and up to 50% of women with infertility. Three types are recognised: superficial peritoneal, ovarian (endometrioma), and deep infiltrating endometriosis (DIE). Risk of malignant transformation (endometrioid and clear-cell ovarian carcinoma) is mainly linked to DIE.

1. BIGGEST CHANGE: End of the "Laparoscopy First" Dogma

Old Standard

Laparoscopy with histological confirmation was the gold standard for diagnosis - patients waited years, went through surgery to even confirm the condition existed.

New Approach (ACOG 2025, ESHRE 2022, NICE 2024, Canadian Guideline 2024)

Clinical diagnosis is now sufficient to initiate treatment in most cases.
A diagnosis can be made based on:
  • Characteristic symptoms (dysmenorrhoea, deep dyspareunia, dyschezia, chronic pelvic pain, infertility)
  • Physical examination (fixed retroverted uterus, tender uterosacral ligaments, deeply infiltrating nodules in POD)
  • Imaging (TVUS, MRI) - especially for endometriomas and DIE
This eliminates diagnostic delay (historically 7-12 years on average) and avoids unnecessary surgery. The Canadian Guideline No. 449 (2024) formally endorsed this, and the US VA is even removing the laparoscopy requirement for service connection (proposed rule, October 2025).
Laparoscopy is still needed when: imaging is negative but symptoms are convincing, surgical intervention is planned, or cancer needs to be excluded.

2. Imaging Advances - "Imaging First"

Transvaginal Ultrasound (TVUS) - Now Standardized

  • The IDEA (International Deep Endometriosis Analysis) group in 2024 expanded its consensus guidelines to include routine evaluation of the parametrium for lateral compartment disease
  • Standardized TVUS protocols now reliably detect DIE, endometriomas, and bowel involvement
  • Pelveoneurosonography - a new technique that visualises sacral nerve roots and plexus, structures implicated in chronic pelvic pain that were previously invisible on standard imaging

MRI - Harmonised Protocols

  • MRI protocols are being standardised internationally for greater consistency in preoperative assessment
  • MRI detects haemosiderin deposits in abdominal organs suggesting DIE; role is strongest for complex or extragenital disease

Molecular Imaging - DETECT Study (Oxford)

A major emerging development: the University of Oxford's DETECT study is evaluating ⁹⁹ᵐTc-maraciclatide, a radiolabelled tracer that binds to the αvβ3 integrin expressed on endometriotic lesion surfaces. This could allow:
  • Non-invasive, functional imaging of active endometriotic lesions
  • Detection of early-stage and superficial peritoneal disease (the one type current imaging still misses)

New ACR Appropriateness Criteria (2024)

The ACR Appropriateness Criteria for Endometriosis (2024) provide updated, evidence-based guidance on when to use TVUS vs MRI vs other modalities for different clinical presentations.

3. Biomarkers - Approaching Clinical Readiness

Why Biomarkers Matter

CA-125 is neither sensitive nor specific enough for routine diagnosis. The search for a reliable blood/saliva/menstrual fluid test has been ongoing for decades. Recent advances show promise:
Biomarker TypeCandidatesStatus
Blood-based microRNAs (miRNAs)Specific miRNA panelsValidation studies published (Nature 2025)
Salivary signature109-miRNA panelHigh sensitivity and specificity in validation studies
Menstrual effluentNeutrophil morphology changes2025 findings - neutrophils signal incorrectly in endometriosis
Serum proteinsVEGF, IL-6, MMP panelsResearch stage
Key 2025 finding: Research published in npj Women's Health (2025) translated miRNA blood-based discovery into a candidate molecular test. Morphological changes in neutrophils in menstrual effluent may serve as a non-invasive diagnostic tool.

Current Reality Check (ESHRE 2025)

No single biomarker yet reliably detects all disease phenotypes, particularly superficial peritoneal lesions. The field still lacks external validation and standardisation - but clinical readiness is "closer than ever" (ESHRE 2025 session, reported in EMJ Reproductive Health 2025).

4. New Drugs - Oral GnRH Antagonists

This is arguably the most clinically impactful update in treatment.

Traditional Medical Options (Still Used)

Drug ClassAgentsRole
NSAIDsIbuprofen, mefenamic acidFirst-line analgesia
Combined OCPAny COCFirst-line hormonal suppression
ProgestogensDienogest, DMPA, LNG-IUSFirst/second line
GnRH agonistsLeuprolide, goserelinSecond-line (injectable, with add-back)
Dienogest vs COC meta-analysis (2025, PMID 40312882): Both are equally effective for pelvic pain. Dienogest is comparable to COC in efficacy and tolerability; COC showed slightly better dyspareunia scores. Choice should be individualised.

NEW: Oral GnRH Antagonists - Second-Line Standard

Three new oral GnRH antagonists now available or approved:
DrugBrandStatusKey Feature
ElagolixOrilissaFDA approved (US); CDSCO approved India (March 2024)Daily oral; dose-dependent hypoestrogenism; ACOG 2025 meta-analysis confirms efficacy
Relugolix + estradiol/norethisteroneRyeqoEMA approved (Europe); MHRA approved (UK)Combined with add-back therapy in a single tablet; prevents bone loss
LinzagolixYseltyEMA approvedOnce daily; flexible dosing
How they differ from GnRH agonists:
  • Immediate suppression (no initial "flare" of estrogen/LH seen with agonists)
  • Oral formulation (vs injectable agonists)
  • Rapid reversibility on stopping
  • Titratable dosing - can balance symptom control vs. side effects (hot flushes, bone loss)
  • All used with add-back hormone therapy to mitigate hypoestrogenic side effects and bone loss
Important India context: CDSCO's Reproductive SEC meeting (March 2024) approved elagolix for endometriosis pain in India under the trade name Orilissa.

5. Aromatase Inhibitors - Confirmed Role in Refractory Cases

Endometriotic implants produce their own estrogen via aromatase (illustrated in the Robbins diagram above). Aromatase inhibitors (letrozole, anastrozole) are now used in combination with hormonal therapy for:
  • Medical castration failures
  • Postmenopausal patients with recurrent disease
  • Deep infiltrating endometriosis refractory to standard therapy

6. Artificial Intelligence in Diagnosis

AI is entering endometriosis diagnostics:
  • Triage role - identifying patients who need specialist imaging or referral
  • Adolescent and fertility patient pathways - accelerating diagnosis in high-risk groups
  • MRI pattern recognition - deep learning models being trained on pelvic MRI datasets
  • TVS analysis - though highly operator-dependent images make AI development harder
Current limitations: small and non-representative training datasets, lack of external validation, inconsistent data quality. Not yet in routine clinical workflows.

7. Endometriosis and Fertility - New Evidence

A major Cochrane-level meta-analysis (Busnelli et al., Hum Reprod Update 2024) separated the independent effects of endometriosis, adenomyosis, and ART-related factors on pregnancy outcomes:
  • Endometriosis independently increases risks of placenta praevia, preterm birth, and SGA neonates
  • IVF outcomes are affected - but less than previously thought when confounders are separated

Endometrioma Surgery Before IVF

A systematic review (Veth et al., Fertil Steril 2024) on endometrioma recurrence after surgery found high recurrence rates without postoperative medical suppression, reinforcing the role of postoperative hormonal therapy to delay recurrence.
  • Ovarian cystectomy (not drainage) still preferred for definitive treatment
  • Preoperative oocyte cryopreservation should be considered for bilateral disease

8. New Classification Needs

Bailey & Love (28th Ed.) notes there is still no internationally accepted classification system for endometriosis. The existing rAFS/rASRM staging correlates poorly with symptoms or fertility outcomes. The Endometriosis Fertility Index (EFI) is validated for predicting fecundity after surgery, but a unified system addressing all clinical domains (pain, fertility, recurrence risk) is still lacking.

9. Psychosocial Recognition - A Formal Update

A systematic review (Rempert et al., Reprod Sci 2024) confirmed the significant psychosocial burden: depression, anxiety, reduced quality of life, relationship difficulties, and occupational impairment. Updated guidelines (ACOG, NICE) now formally recommend psychological support and patient education as part of the care pathway - not an afterthought.
An innovative 2025 meta-analysis (González-Lara et al., JMIG 2025) on immersive virtual reality (VR) for endometriosis-related pelvic pain showed meaningful reduction in pain scores, adding a new non-pharmacological option for pain management.

10. Global Prevalence - Updated Estimates

A 2025 global systematic review and meta-analysis (Wang et al., Reprod Biol Endocrinol 2025) revised global prevalence estimates for endometriosis and adenomyosis together, highlighting that the conditions co-exist in a substantial proportion of women, reinforcing the need to screen for both when either is suspected.

Summary Table: Key 2024-2025 Changes

DomainOld PracticeNew in 2024-2025
DiagnosisLaparoscopy requiredClinical diagnosis sufficient; imaging first
ImagingTVUS for endometriomas onlyStandardised TVUS/MRI; parametrium assessment; pelveoneurosonography
Molecular imagingNoneDETECT study: ⁹⁹ᵐTc-maraciclatide tracer in trials
BiomarkersCA-125 (poor)miRNA panels, salivary 109-miRNA signature; menstrual effluent neutrophils
New drugsGnRH agonist injectionsOral GnRH antagonists: elagolix, relugolix, linzagolix approved
AINot in useTriage, imaging analysis - research stage
Pain: non-pharmaPhysiotherapy, psychologyVR immersive therapy - promising new evidence
FertilityEmpiric riskIndependent risks quantified from ART data
PsychosocialRarely addressed formallyFormal guideline recommendation for psychological support

All tests for checking ovarian reserve

Ovarian reserve refers to the quantity and quality of remaining follicles/oocytes in the ovary. Key tests include AMH (best single marker), antral follicle count on ultrasound, basal FSH, estradiol, and dynamic challenge tests like the clomiphene citrate challenge test.
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"ovarian reserve" AMH antral follicle count testing

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ovarian reserve tests AMH AFC FSH inhibin B complete list clinical use 2024 2025

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