What are the major risks of dilatation and evacuation (D&E)?

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Last updated: September 18, 2025View editorial policy

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Major Risks of Dilatation and Evacuation (D&E)

The principal complications of dilatation and evacuation (D&E) include perforation, hemorrhage, and infection, with uterine perforation being the most serious risk occurring in approximately 1-3% of cases.

Primary Risks

1. Uterine Perforation

  • Occurs in approximately 1-3% of D&E procedures 1
  • More likely to occur:
    • During cervical dilation phase
    • With less experienced operators
    • In complex cases (e.g., advanced gestations)
  • May require laparotomy to repair the defect and evaluate for injury to adjacent organs 2
  • Can lead to damage to surrounding structures including bowel, bladder, or blood vessels
  • Signs of perforation include:
    • Pain
    • Bleeding
    • Visualization of omentum or bowel in the suction curette 2

2. Hemorrhage

  • Risk increases with:
    • Advanced gestational age
    • Uterine anomalies
    • Previous uterine surgery
    • Placenta previa or accreta
  • May require blood transfusion in severe cases
  • Can be immediate or delayed

3. Infection

  • Post-procedure infection rates of approximately 1-3% in uncomplicated cases 1
  • Significantly lower infection rates compared to other pregnancy termination methods (1.3% after D&E vs. 23.9% with induction of labor) 1
  • Risk factors include:
    • Pre-existing genital tract infections
    • Retained products of conception
    • Inadequate sterile technique

Secondary Risks

1. Cervical Trauma/Laceration

  • More common with:
    • Inadequate cervical preparation
    • Rapid dilation
    • Advanced gestational age

2. Retained Products of Conception

  • Can lead to:
    • Delayed bleeding
    • Infection
    • Need for repeat procedure

3. Anesthesia-Related Complications

  • Risks associated with sedation or general anesthesia
  • Includes respiratory depression, aspiration, and allergic reactions

Risk Reduction Strategies

1. Adequate Cervical Preparation

  • For procedures at 20-24 weeks, at least one day of cervical preparation with osmotic dilators is recommended 3
  • Adjunctive medications can be considered:
    • Mifepristone administered one day pre-operatively makes D&E subjectively easier at 20-24 weeks without increasing side effects 3
    • Misoprostol can be used but may cause more side effects like pain and nausea compared to mifepristone 3

2. Provider Experience

  • Risk of complications is lower with experienced providers
  • Training and adequate case volume are important factors in reducing complications

3. Infection Prevention

  • Proper sterile technique during the procedure
  • Screening and treatment of pre-existing infections before the procedure
  • Consideration of prophylactic antibiotics in high-risk cases 1
  • Complete evacuation of uterine contents to prevent retained tissue 1

4. Procedural Setting

  • High-risk patients should be managed in an experienced center with on-site surgical support 4
  • Procedures should be performed in a facility with emergency support services available

Patient Monitoring and Follow-up

  • Patients should be closely monitored post-procedure for:

    • Vital signs
    • Bleeding
    • Pain
    • Signs of infection
  • Patient education should include warning signs requiring immediate medical attention:

    • Fever
    • Increasing abdominal pain or tenderness
    • Foul-smelling vaginal discharge
    • Prolonged or heavy bleeding
    • Malaise or flu-like symptoms 1

Despite these risks, when performed by experienced providers with appropriate techniques, D&E has been shown to have lower overall complication rates compared to other second-trimester abortion methods such as induction with saline or prostaglandins 5.

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.

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