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COMPARING MANAGEMENT OPTIONS FOR EPL

Clinically stable people can choose among the following management options to achieve completion of EPL, or switch from one to another during the process:

  • Expectant management (“watchful waiting”)
  • Medication management with misoprostol, adding mifepristone where available
  • Aspiration in an outpatient or operating room setting

Choosing from among these options is a preference-sensitive decision (Shorter 2018), as each option is safe and relatively effective, and greater satisfaction is reported when treated according to preference.

Studies show a wide range of success rates for expectant and medication management, varying by type of EPL, US vs clinical endpoints, and management timing (i.e. when aspiration is offered). Expectant management is more successful when the process of expulsion has already begun, compared to other types of EPL. Cliniciansshould offer counseling specific to the type of EPL (anembryonic, EPL in progress, etc.), success rates (see Comparison Table below), and the time they are willing to wait until completion.

Expectant Management

Expectant or spontaneous completion of EPL can be offered to those who are clinically stable, for 6-8 weeks if they remain stable and amenable. “Watchful waiting” may avoid intervention and attendant side effects or complications (Nanda 2012; See Table below).

Clinicians may reassess every 1-2 weeks by telehealth or in-person to monitor progress and confirm continued preference for expectant management vs. another option for faster resolution. Pain and other symptom management can be addressed similarly to medication abortion (see Ch. 4: Pain Management).

Given slightly increased rates of bleeding with expectant vs. aspiration management (Ghosh 2021), people with anemia (e.g. hgb < 9) or those with other bleeding risks (i.e. bleeding disorders or use of anticoagulants) may be best managed with aspiration (Nanda 2012). Clinicians should also consider additional factors that may impact safety such as local laws/policies, risk for criminalization if higher level of care is indicated urgently, and potential need for travel to or from more or less restricted areas.

Medication Management

Medication management offers a shorter, more predictable time to completion with less follow up when compared to expectant management, avoids uterine aspiration, and is a cost-effective outpatient option that may be available through a primary care clinician. Pain and other symptom management can be addressed similarly to medication abortion (see Ch. 4: Pain Management). Prophylactic antibiotics are not recommended for medication management of EPL (SFP 2025).

Mifepristone and Misoprostol

Treatment with mifepristone 200 mg orally followed by misoprostol results in a higher likelihood of successful EPL management than treatment with misoprostol alone (relative risk 1.25), with significantly less likelihood of uterine aspiration (relative risk 0.37), and a trend toward less bleeding (Schreiber 2018, Dzuba 2015). Additional cost of mifepristone is usually offset by fewer follow-up visits. If presenting with heavier bleeding (≥2 pads/hour), may skip Mifepristone, add Motrin, and seek ER care if no improvement in 1 hour. Misoprostol is dosed 7-48 hours after mifepristone, much like with medication abortion. Mifepristone requires one clinician in an organization to register with a mifepristone manufacturer (See Ch. 4: Medication Abortion).

Mifepristone-Misoprostol Dosing for EPL Management (Schreiber 2018, SFP 2025)

Mifepristone 200 mg oral followed by

Misoprostol 800 mcg vaginally, buccally, or sublingually in 7-48 h1,2,3

(if heavy bleeding has already commenced, may use misoprostol sooner and avoid vaginal use)

1. Highest success rates: vaginal misoprostol taken between 7-20h after mifepristone (Flynn 2021)
2. 800mcg misoprostol should be repeated 4 hours later if > 9 weeks or if no bleeding < 9 weeks
3. Sublingual dosing safe and effective, but may be associated with higher side effect profile

Misoprostol Alone

Misoprostol alone is effective and safe in treating EPL, when mifepristone is not available or covered. Although dosing guidelines vary, evidence supports that the misoprostol doses below are equally effective for managing incomplete EPL (Do 2020, Kim 2017). Some studies show higher levels of bleeding and more follow-up with misoprostol compared to aspiration (Davis 2007, Ghosh 2021, Zhang 2005), so individuals with severe anemia (Hgb <9) or bleeding risk factors may be best managed with aspiration (See Chapter 3: Hemorrhage Risk Factors).

Misoprostol Only Dosing for EPL Management (Tarleton 2025)
2 or more doses 600-800 mcg sublingual or vaginal q 3 h

Uterine Aspiration

Uterine aspiration is the most definitive and rapid EPL management option and has the highest success rate (Ghosh 2021). Aspiration may be chosen to avoid medication side effects or for expedited procedural care in the office. MVA or EVA can be performed safely in the outpatient office or the ED. Costs and bleeding-related complications are greater in the OR vs. office settings, and may add unnecessary patient burdens (Dalton 2006). If uterine aspiration is used to manage EPL, there is moderate evidence for the use of prophylactic antibiotics (ACOG 2018, Islam 2021, SFP 2025). See Chapter 6: Aspiration Steps.

Comparison of Management Options for EPL

Advantages Disadvantages Estimated Rates of Success
Expectant Management
  • Non-invasive; body expels products of conception
  • Perceived as natural by some patients
  • Avoids anesthesia and procedural risks if successful
  • Process is unpredictable; can last days to weeks
  • Can have prolonged or heavy bleeding and cramping, typically up to 8 weeks
  • Despite waiting, nearly ⅓ still require medication or uterine aspiration to complete
Incomplete EPL:

  • Day 7: 50%
  • Day 14: 70-85%
  • Day 46: 90%

Other types of EPL:

  • Day 7: 23-30%
  • Day 14: 35-60%
  • Day 46: 65-75%

(Casikar 2010, Nanda 2012, Kim 2017)

Medication Management

(Mifepristone 200 mg followed by Misoprostol 800mcg PV in 7-48h)

  • Non-invasive
  • Highly effective
  • Shorter course (full resolution usually within 8-14 days)
  • Avoids anesthesia and procedural risks if successful
  • Cost-effective
  • May cause heavier or stronger cramping than aspiration
  • May cause short-term side effects (nausea, vomiting, diarrhea, fever)
  • May still need uterine aspiration
  • Uncommonly, may still need uterine aspiration
Incomplete EPL:Complete expulsion:

  • Data lacking on efficacy of mifepristone regimen

Other types of EPL:

  • Mife plus 800 mcg misoprostol 84% vs. misoprostol alone 67%

(Dzuba 2015, MacNaughton 2021,
Schreiber 2018)

Medication Management

(Misoprostol 600-800 mcg SL or PV q3h until expulsion)

  • As above
  • Cost-effective (less expensive than mife/miso if patient is paying for the meds)
  • As above
  • May be less effective than mifepristone regimen depending on the type of EPL and number of doses
  • SL route may have more GI and systemic SE than vaginal route
  • Increased side effects with more doses given
Incomplete EPL:

  • Single Dose 96%

Other types of EPL:

  • Single Dose 71%
  • Second Dose 84%
  • Every 3 hours x 2-3 doses: 88-92%
  • Higher efficacy when no embryo/fetus or cardiac activity detected on US

(Ipas 2021, Kim 2017, Neilson 2013, Ngoc 2013, Tang 2003, Zhang 2005)

Office-based Aspiration
  • Predictable
  • Fastest resolution
  • Less bleeding than expectant or medication
  • Low probability of further treatment need (<5%)
  • Pain management with local plus oral or IV meds
  • Better cost & resource savings than OR
  • Improved patient access, continuity and privacy
  • Less patient & staff time, compared to OR



  • Rare procedural risks
  • Fewer pain control options in some settings compared to OR procedure
  • 98-100%

(Nanda 2012)

OR Aspiration
  • Can use deep sedation or general anesthesia
  • Predictable, prompt resolution
  • Less time/bleeding than expectant or medication
  • Low probability of further treatment need (<5%)
  • More cost, time, exams than office-based procedures
  • Rare procedural risks; general anesthesia risks
  • 98-100%

(Nanda 2012)

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