What complications are classified as adverse pregnancy outcomes?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: April 6, 2026 • View editorial policy

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.

Adverse Pregnancy Outcomes: Classification and Definition

Adverse pregnancy outcomes (APOs) are complications affecting maternal or fetal health during pregnancy, delivery, or the immediate postpartum period, and include: stillbirth, preterm birth (<37 weeks), small-for-gestational-age (SGA) infants, intrauterine growth restriction (IUGR), hypertensive disorders of pregnancy (preeclampsia, eclampsia, gestational hypertension, HELLP syndrome), gestational diabetes, placental abruption, low birth weight infants, pregnancy loss/miscarriage, and neonatal death.

Core Adverse Pregnancy Outcomes

The most consistently recognized APOs across guidelines include:

Fetal/Neonatal Outcomes

  • Stillbirth: Fetal death from ≥20 weeks of gestation 1
  • Preterm birth: Delivery <37 completed weeks of gestation, with particularly high risk when <34 weeks 1
  • Small-for-gestational-age (SGA): Infant birthweight below the 10th percentile for gestational age and sex, used as a proxy for fetal growth restriction 1
  • Intrauterine growth restriction (IUGR): Estimated fetal weight <10th percentile for gestational age, often related to suboptimal uterine-placental perfusion 2
  • Low birth weight: Infants with reduced weight at delivery 3
  • Neonatal death: Death within the first 28 days of life 4
  • Congenital malformations and congenital heart block 4

Maternal Outcomes

  • Hypertensive disorders of pregnancy: Including preeclampsia (new-onset hypertension with proteinuria after 20 weeks), eclampsia (preeclampsia with seizures), gestational hypertension, HELLP syndrome (hemolysis, elevated liver enzymes, low platelets), and chronic hypertension in pregnancy 3, 5, 6
  • Gestational diabetes mellitus: Glucose intolerance with onset or first recognition during pregnancy 5, 7
  • Placental abruption: Premature separation of placenta from uterus before fetal delivery 5, 7
  • Pregnancy loss/miscarriage: Spontaneous pregnancy loss, with recurrent pregnancy loss defined as ≥2 spontaneous miscarriages 5
  • Maternal mortality and severe maternal morbidity 3, 8

Clinical Significance

These outcomes are not isolated events but interconnected complications sharing common pathophysiology, particularly placental insufficiency 1. Women experiencing any APO have a 3-fold increased risk of developing cardiovascular disease risk factors within 2 years postpartum 9, with the strongest associations seen between:

  • Gestational diabetes and subsequent type 2 diabetes (21-fold increased risk) 9
  • Preeclampsia and chronic hypertension (6-fold increased risk) 9

The recurrence risk is substantial: women with prior stillbirth have a 4-fold increased recurrence risk, those with preterm birth have 2.5- to 10.6-fold increased recurrence (nearly 14-fold for PTB <34 weeks), and those with SGA have at least an 8-fold increased recurrence risk 1.

Long-Term Implications

APOs serve as markers for future cardiovascular disease, with women experiencing these complications showing increased risk of stroke (1.74-fold for any hypertensive disorder of pregnancy), myocardial infarction, and cardiovascular mortality that persists for over 40 years after delivery 10, 5, 11. The 2024 AHA/ASA stroke prevention guideline specifically recommends screening for APO history followed by evaluation and management of vascular risk factors 5.

Important Caveats

While these outcomes are traditionally viewed as separate entities, they frequently co-occur and share common antecedents. SGA accounts for up to 50% of preventable stillbirths 1, and many preterm infants are growth restricted 1. The presence of multiple APOs compounds future cardiovascular risk 12. Definitions may vary slightly between studies and healthcare systems, but the core outcomes remain consistent across international guidelines 1, 4, 5, 6.

References

Research

Lifetime Adverse Pregnancy Outcome History and Cardiovascular Risk.

Hypertension (Dallas, Tex. : 1979), 2026

Related Questions

What additional work‑up or monitoring is recommended for a spleen measuring 13 cm in maximal diameter?
What procedure might be needed for a 17-year-old male presenting with hematuria?
Ten weeks after hyperthermic intraperitoneal chemotherapy (HIPEC), I have diarrhea, abdominal cramping, and occasional blood in the stool without fever—what are the likely causes and recommended evaluation and management?
What is the appropriate acute management for a 12-year-old female presenting with suicidal ideation?
How should a 1 cm popliteal (behind‑the‑knee) lymph node be evaluated and managed?
Can dexmedetomidine (Precedex) be used for sedation in patients with intracerebral hemorrhage, and what are the recommended dosing and monitoring parameters?
In a patient who has recovered from poliomyelitis, are there any contraindications to performing spinal anesthesia?
In a patient with acute ischemic stroke due to left middle cerebral artery M1 large‑vessel occlusion secondary to cardioembolism from severe rheumatic mitral stenosis, with no hemorrhagic transformation on imaging, what is the earliest safe time to start oral anticoagulation according to guidelines, randomized trials, or meta‑analyses, and which anticoagulant and initiation/titration protocol is recommended?
What is the significance of an elevated monocyte count in cerebrospinal fluid?
Should Dayvigo (lemborexant) be taken daily or as needed (PRN) to be effective?
How should a left bundle branch block (LBBB) be evaluated and managed in a pregnant patient?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.