Retained placenta

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"retained placenta" management

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Now I have comprehensive information from multiple authoritative textbooks. Here is a complete overview of retained placenta:

Retained Placenta

Definition

Retained placenta is failure of the placenta to deliver within 30 minutes after birth of the baby (some definitions use 60 minutes). It is one of the "four Ts" of postpartum hemorrhage — specifically under Tissue — and accounts for up to 10% of postpartum hemorrhages.

Mechanism of Normal Placental Separation

Following fetal delivery, myometrial contractions shear the placenta from the implantation site; the spiral arteries are mechanically constricted by uterine contraction. Retained placenta prevents this constriction, leading to ongoing hemorrhage.

Risk Factors

  • Maternal age > 30 years
  • Preterm delivery (24–26 weeks gestation has the highest risk compared to term)
  • Stillbirth
  • Multiparity
  • Prior uterine surgery / cesarean section
  • Placenta previa
  • History of uterine curettage
  • Uterine anomalies
  • Succenturiate (accessory) placental lobes — any defect in the delivered placenta may signal a retained cotyledon

Causes

CauseMechanism
Adherent placenta (most common)Defective decidua basalis — chorionic villi attach to or invade myometrium
Placenta accretaVilli adhere to myometrium without invading decidua basalis
Placenta incretaVilli extend into myometrium
Placenta percretaVilli penetrate full myometrial thickness
Trapped/incarcerated placentaCervical closure before placental expulsion
Retained cotyledon/membraneIncomplete delivery — fragment remains after main placenta delivered
The current incidence of placenta accreta is approximately 3/1,000 deliveries, with a strong association with prior cesarean delivery.

Clinical Consequences

  • Primary postpartum hemorrhage (within 24 hours)
  • Secondary postpartum hemorrhage (24 hours to 6 weeks)
  • DIC — retained products contain excess thromboplastin, which can precipitate disseminated intravascular coagulation
  • Endometritis / sepsis — retained tissue is a nidus for infection
  • Uterine subinvolution
Always inspect the delivered placenta for missing cotyledons or a ragged maternal surface, which indicates retained fragments.

Management

Step 1 — Initial Stabilisation

  • IV access (large-bore), fluid resuscitation
  • Monitor vital signs, Foley catheter (decompresses bladder, monitors output)
  • Cross-match blood; have blood products available
  • Administer tranexamic acid 1 g IV

Step 2 — Attempt Placental Delivery

  • Controlled cord traction + uterine massage (Brandt–Andrews manoeuvre)
  • Oxytocin — 10 units IM after delivery, or 5–10 units IV followed by infusion up to 40 units total
  • Consider misoprostol in low-resource settings when oxytocin is unavailable

Step 3 — Tocolysis + Manual Removal (if placenta undelivered after 30 min)

Manual removal under regional or general anaesthesia is standard.
Nitroglycerin is particularly useful as a tocolytic to relax the uterus:
  • Translingual spray: 400-μg pre-metered spray, 1–2 sprays every 3–5 min (maximum 3 doses in 15 min)
  • IV injection: 50–150 μg, repeated in 30–60 seconds if blood pressure is stable
Manual Removal Technique:
  1. Trace the umbilical cord through the cervical os to the placental margin
  2. Digitally perforate the placental membranes
  3. Gradually separate the placenta from the myometrium using blunt dissection
  4. Explore the uterus for retained cotyledons after removal
  5. Curettage by an obstetrician for remaining fragments
  6. Stimulate uterine contraction: massage + oxytocin + prostaglandins
⚠️ Placenta accreta, increta, and percreta are not digitally dissectible — attempting forced removal risks catastrophic hemorrhage.

Step 4 — Management of Abnormally Invasive Placenta (Accreta Spectrum)

  • If placenta cannot be manually removed → suspect accreta spectrum disorder
  • Hysterectomy is usually required to avoid catastrophic haemorrhage
  • Conservative approach (only if fertility preservation is paramount):
    • Curettage of retained placenta, OR suturing of the bleeding site (at cesarean)
    • Prophylactic selective uterine artery embolisation — described for diagnosed cases before delivery
    • Must be prepared to proceed to hysterectomy if bleeding is not promptly controlled

Step 5 — Adjuncts for Uncontrolled Bleeding

  • Pelvic vessel embolisation (interventional radiology): reported success 95–100%; preserves fertility
  • Uterine packing (gauze or Foley catheter): temporising measure when embolisation/hysterectomy unavailable
  • Recombinant factor VIIa: used in severe, refractory postpartum haemorrhage

Antibiotics

Prophylactic antibiotics at the time of manual placental removal have been debated; a 2024 Cochrane systematic review evaluated this specifically. Their role is not firmly established by current evidence for routine use, though they are widely given in practice given the infection risk.

Key Points Summary

FeatureDetail
Time threshold> 30 minutes after delivery
Contribution to PPH~10% of cases
Uterotonic of choiceOxytocin (IV/IM); misoprostol in resource-limited settings
Tocolytic for manual removalNitroglycerin (IV or translingual)
Anaesthesia for manual removalRegional or general
When to suspect accretaPlacenta non-dissectible on manual removal
Definitive treatment for accretaHysterectomy

Sources:
  • Creasy & Resnik's Maternal-Fetal Medicine: Principles and Practice, Chapter 40
  • Rosen's Emergency Medicine, Chapter on Postpartum Hemorrhage
  • Pfenninger and Fowler's Procedures for Primary Care, Maternal Complications
Recent evidence (2024 Cochrane reviews):
  • Uterotonics for retained placenta management [PMID: 39465684]
  • Prophylactic antibiotics for manual removal of retained placenta [PMID: 39474979]

Anemia mukth bharat

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Anemia Mukt Bharat programme India details 2025

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Anemia Mukt Bharat 6x6x6 strategy beneficiaries targets

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Anemia Mukt Bharat 6x6x6 strategy interventions beneficiaries institutional mechanisms targets progress

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Anemia Mukt Bharat 6 institutional mechanisms 6 interventions complete list IFA schedule

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6 institutional mechanisms 6 interventions IFA schedule deworming beneficiaries

Here is a comprehensive overview of Anemia Mukt Bharat (AMB):

Anemia Mukt Bharat (AMB)

Background

  • Launched in 2018 by the Ministry of Health and Family Welfare (MoHFW), Government of India
  • Builds upon earlier programmes: National Iron Plus Initiative (NIPI, 2013) and Weekly Iron Folic Acid Supplementation (WIFS)
  • Implemented under POSHAN Abhiyaan (National Nutrition Mission)
  • Integrated with the School Health Programme and National Deworming Day
  • Implemented across all villages, blocks, and districts in all States/UTs

Burden of Anemia in India (NFHS-5, 2019–2021)

Population GroupPrevalence
Children (6–59 months)67.1%
Adolescent girls59.1%
Women of reproductive age~57%
Non-pregnant women~30% (539 million)
Pregnant women~37% (32 million)
3 in 4 Indian womenLow dietary iron intake

Goal

Reduce anemia prevalence by 3 percentage points per year across all target groups, following a life cycle approach.
Reach approximately 450 million beneficiaries — nearly 50% of India's population.

The 6×6×6 Strategy

The core framework of AMB consists of 6 beneficiary groups × 6 interventions × 6 institutional mechanisms.

1️⃣ Six Target Beneficiary Groups

#GroupAge
1Pre-school children6–59 months
2School-age children5–9 years
3Adolescent girls and boys10–19 years
4Women of reproductive age (non-pregnant, non-lactating)15–49 years
5Pregnant women
6Lactating mothers

2️⃣ Six Interventions

#Intervention
1Prophylactic Iron and Folic Acid (IFA) Supplementation
2Periodic Deworming
3Intensified year-round Behaviour Change Communication (BCC) Campaign (including assured delayed cord clamping)
4Testing of anemia using digital non-invasive haemoglobinometers + point-of-care treatment
5Mandatory provision of IFA-fortified foods in government-funded public health programmes
6Addressing non-nutritional causes of anemia in endemic pockets (malaria, haemoglobinopathies, fluorosis)

IFA Supplementation Schedule (Colour-Coded)

GroupFormulationFrequencyColour
Children 6–59 monthsIFA syrup (1 mL)Bi-weekly (2×/week)
Children 5–9 years (WIFS-Junior)IFA tabletWeeklyPink
Adolescents 10–19 yearsIFA tabletWeeklyBlue
Women of reproductive age (20–49 yrs)IFA tabletWeeklyRed
Pre-conception / 1st trimesterFolic acid tabletDaily
Pregnant women (from 2nd trimester)IFA tabletDaily— (continues 6 months postpartum)
Lactating womenIFA tabletDaily (for 6 months)

3️⃣ Six Institutional Mechanisms

#Mechanism
1Strengthening procurement and supply chain for IFA supplements
2Capacity building and training of all stakeholders
3Inter-ministerial convergence (MoHFW + Ministry of Education + Ministry of Women & Child Development + Ministry of Food & Supplies)
4AMB Dashboard/Digital Portal — real-time tracking of anemia screening, IFA supply and distribution
5Demand generation through community mobilisation (ASHA, AWW, ANM)
6Monitoring, reporting, and review mechanisms (AMB Scorecard with key performance indicators)

Digital Tools

  • AMB Dashboard: tracks real-time data on IFA supply, distribution, screening coverage at national, state, district, and block levels
  • Digital haemoglobinometers: non-invasive point-of-care testing at schools and health facilities
  • States use the AMB scorecard to finalize budgets and procurement plans

Recent Progress (2024–25)

  • 15.4 crore (154 million) children and adolescents received IFA supplements in Q2 FY 2024–25
  • Significant improvement in IFA coverage among children, lactating mothers, and pregnant women (2018–19 to 2022–23)
  • Programme is being continuously evaluated through the AMB Index — a composite state-level performance ranking

Key Programme Mnemonics

AMB ToolFull Form
TESTScreen with haemoglobinometer
TREATPoint-of-care treatment for anemia
TALKBCC — counselling and awareness
SUPPLYIFA supply chain management
DASHBOARDReal-time digital monitoring

Challenges

  • Irregular IFA supply at district/block level
  • Poor compliance due to side effects (nausea, GI upset)
  • Non-nutritional causes (malaria, thalassaemia, fluorosis) not addressed by IFA alone
  • Gaps in coverage of out-of-school adolescents
  • Data quality issues in reporting

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