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Overview of pregnancy termination

Overview of pregnancy termination
Authors:
Jody Steinauer, MD, MAS
Rajita Patil, MD, FACOG
Section Editor:
Robert L Barbieri, MD
Deputy Editor:
Alana Chakrabarti, MD
Literature review current through: Feb 2022. | This topic last updated: Jan 13, 2022.

INTRODUCTION — Access to safe abortion care and family planning services is an integral component of health care. This topic will review general issues regarding pregnancy termination, including preprocedure evaluation, choice of method, and complications. Techniques for first- and second-trimester procedures are discussed separately.

(See "First-trimester pregnancy termination: Uterine aspiration".)

(See "First-trimester pregnancy termination: Medication abortion".)

(See "Overview of second-trimester pregnancy termination".)

EPIDEMIOLOGY — Worldwide, the estimated rate for abortion from 2010 to 2014 was 35 per 1000 females ages 15 to 44 [1]. The rate in resource-rich countries was 27 per 1000 and in resource-limited countries was 37 per 1000. The highest rate was in the Caribbean (65 per 1000), and the lowest rate was in North America (17 per 1000) and northern or western Europe (18 per 1000). An estimated 25 percent of pregnancies worldwide ended in induced abortion. Similarly, in the United States, close to one in four females will have an abortion during their reproductive life [2].

Data specific to the United States from the Centers for Disease Control and Prevention (CDC) in 2018 include [3]:

Overall abortion rates – The rate of pregnancy termination was 11.3 per 1000 females ages 15 to 44 years, or 189 per 1000 live births. While there was a 1 percent increase in the rate of abortions from 2017, the overall rate has decreased steadily over the past two decades. The CDC figures are based on data voluntarily reported to state health agencies and may be incomplete.

Abortion rates by age group – Abortion rates were highest for ages 20 to 24 (19.1 per 1000 females) and 25 to 29 (18.5 per 1000 females). The rate of abortion in adolescents was 6 per 1000 females for those ages 15 to 19 compared with 0.4 per 1000 females for those ages <15 years.

Impact of specific demographic factors – Most terminations were in unmarried patients (85 percent) and those who had one or more children (59 percent). Forty percent of abortions were in patients who had had a prior abortion.

Racial disparities – Abortion rates per 1000 females by racial and ethnic groups were 6.3 for non-Hispanic White Americans, 21.2 for non-Hispanic Black Americans, 11.9 for other races, and 10.9 for Hispanic American females.

Distribution by age of gestation – The vast majority of pregnancy terminations were performed in the first trimester: 78 percent at ≤9 weeks and 92 percent at ≤13 weeks of gestation. For later gestational ages, 6.9 percent of abortions were performed at 14 to 20 weeks and 1 percent at ≥21 weeks.

Potential barriers to early abortion include delay in recognition and confirmation of pregnancy, maternal or fetal complications that are diagnosed or develop after the first trimester, expense, parental involvement laws (see 'Legal issues' below), and lack of access to an abortion provider [4]. Among all United States counties in 2014, 90 percent had no abortion provider [2].

Distribution of procedure type – For procedures occurring at 9 weeks of gestation or less, medication abortion accounted for approximately 39 percent of patients. For gestational ages of ≥14 weeks, most abortions were surgical; ≤2.2 percent used other methods.

PREPROCEDURE EVALUATION

Counseling and informed consent — Counseling should include a nondirective discussion of alternatives (ie, continuing pregnancy with parenting or adoption) and a thorough discussion of the medical and surgical options for pregnancy termination, including the risks, benefits, and expected outcome of each. (See "Counseling in abortion care".)

Legal issues — Abortion providers should be aware of relevant federal and state abortion regulations so they can provide appropriate treatment for their patients. In the United States, for example, some states have instituted a variety of policies that create barriers to abortion access and impact clinical care. Some states have mandatory waiting times between when the patient is counseled and the actual procedure, require parental notification or consent for abortions in minors (minors have the right to seek a court order authorizing the procedure) [5], or mandate that specific topics (some of which are medically inaccurate) be covered in the counseling session. States with these legal restrictions, in addition to areas with limited access to available services, are associated with decreased rates of abortion and higher rates of abortion-related maternal mortality than states without these restrictions [4,6]. A summary of United States abortion laws can be found through the Guttmacher Institute.

Furthermore, in the United States, mifepristone (a progesterone receptor antagonist used for medical and second trimester surgical abortions) is available only with Risk Evaluation and Mitigation Strategy (REMS) restrictions [7]. However, such restrictions may not reduce adverse events or abortion rates. In a retrospective study including over 300,000 abortions performed in Canada, those performed before and after mifepristone was available and with and without REMS-like restrictions had similarly low rates of severe adverse events (eg, blood transfusion, abdominal surgery, admission to an intensive care unit, sepsis) and other complications [8]. In addition, while the rate of medication abortion increased after REMS-like restrictions were lifted, the overall rate of abortion remained stable.

History and physical examination — A targeted medical history is obtained focusing on obstetric, gynecologic, relevant medical (eg, cardiovascular disease, bleeding or clotting disorders), surgical, and psychosocial history.

For in-person visits (see 'Procedure setting' below), a focused physical examination is performed, as appropriate for the patient.

Determining gestational age — Determining the correct gestational age with menstrual dating or ultrasound evaluation is a critical part of preabortion care.

Menstrual dating – Menstrual dating should only be used in patients in whom the first day of the last menstrual period (LMP) is known with certainty and in those with regular menstrual cycles. When menstrual dating is used, the gestational age is estimated based on the interval from the LMP and, prior to surgical abortion, is confirmed by bimanual examination and/or ultrasound.

Evidence shows that in patients with regular menstrual cycles and a known LMP, gestational age as predicted by menstrual dating compared with ultrasound dating are similar [9,10]. In a systematic review including three studies comparing determination of gestational age by LMP or ultrasound, 2.5 to 11 percent of patients who were eligible for medication abortion by LMP became ineligible after ultrasound evaluation [9]; lower rates were reported when gestation was <63 days (63 of 4008 [1.6 percent] patients; one study) [11]. (See "Prenatal assessment of gestational age, date of delivery, and fetal weight", section on 'Clinical assessment of gestational age'.)

Pelvic ultrasound examination – While pelvic ultrasound examination may be helpful and is commonly used by abortion providers in the United States, it is not a requirement for first-trimester abortion, and most abortion care outside of the United States is without ultrasound. The clinical policy guidelines of the National Abortion Federation (NAF), a professional organization of abortion providers in the United States, Canada, Mexico, and Colombia, as well as the American College of Obstetrics and Gynecology (ACOG), do not mandate ultrasound preceding abortion in the first trimester since doing so is not always necessary or even helpful and might impede access to abortion in underserved regions where ultrasound is unavailable [12,13].

Ultrasound examination is useful if patients are uncertain of their dates, have irregular periods, their uterine size is inconsistent with menstrual dates, or their uterine size cannot be adequately assessed. Ultrasound is also used to diagnose ectopic and nonviable pregnancies. (See "Prenatal assessment of gestational age, date of delivery, and fetal weight", section on 'Sonographic assessment of gestational age' and 'Ectopic pregnancy' below.)

We perform a preprocedural ultrasound prior to all second-trimester abortions.

Laboratory testing

Urine or serum human chorionic gonadotropin (hCG) measurement – Urine hCG is often used to confirm pregnancy; if there is concern for an abnormal pregnancy (eg, ectopic), serum hCG should be determined. A patient's own positive home urine pregnancy test may be used as pregnancy confirmation and does not require repetition.

The various types of urine or serum hCG tests are discussed in detail elsewhere. (See "Clinical manifestations and diagnosis of early pregnancy", section on 'Types of pregnancy tests'.)

Hemoglobin or hematocrit – Many practices determine hemoglobin/hematocrit selectively rather than routinely prior to pregnancy termination. In our practice:

For patients at ≤9 weeks, we only check hemoglobin or hematocrit if the patient has a history of anemia (and no result is available from the past 6 to 12 months) or if we are drawing blood for another indication (hCG or Rh typing). If drawn for a patient with a history of anemia, there is no definitive cutoff value at which we prefer a surgical, rather than medication, abortion, and the decision is left to the discretion of the provider. If the patient has a hemoglobin drawn because other laboratory tests are indicated, we do not wait for the result before providing the medication abortion or discharging the patient from clinic.

For patients ≥10 weeks, we test routinely and wait for the results; hemoglobin values ≤9 g/dL are considered a relative contraindication to a medication abortion (given the increased risk for a clinically significant drop in hemoglobin at this gestation), and a surgical abortion is recommended.

Rh typing – RhD status should be determined if the gestation is ≥56 days. While RhD status was historically performed on all patients, evidence shows risk of alloimmunization of D-negative patients to be negligible for gestations <56 days [14-17].

Administration of anti-D immune globulin for Rh-negative patients at ≥56 days is discussed below. (See 'Alloimmunization prevention' below.)

Chlamydia and/or gonorrhea – Screening for chlamydia and gonorrhea should be based on the United States Preventive Services Task Force and Centers for Disease Control and Prevention (CDC) guidelines, which recommend screening of all sexually active patients <25 years old and patients at increased risk of infection, regardless of age. (See "Screening for sexually transmitted infections", section on 'Females'.)

Plan for contraception — Ovulation can occur soon after an abortion and before the onset of menses; thus, we recommend that contraception counseling occur prior to the abortion procedure. Contraception can usually be initiated the day of the procedure. (See "Contraception: Postabortion", section on 'Initiation of contraception'.)

CHOICE OF PROCEDURE — The choice of procedure type (ie, medication, surgery) depends on gestation, patient preferences, clinician experience, availability of services, and legislative barriers. All options are safe and effective for appropriately selected patients.

First trimester

How to choose — Ideally, patients seeking first-trimester abortion care should have access to both medication and surgical abortion and be counseled about the benefits and limitations of each. Factors that contribute to this choice include:

Gestational age – The US Food and Drug Administration (FDA) approves mifepristone in combination with misoprostol for medication abortion up to 70 days (≤10 weeks) of gestation [18]. The National Abortion Federation (NAF) and Planned Parenthood Federation of America support its use up to 77 days (11 weeks) [19]. Patients >11 weeks are not currently eligible for first-trimester medication abortion with mifepristone. Misoprostol-only regimens may be used in settings in which mifepristone is not available or is too costly. This is discussed in detail separately. (See "First-trimester pregnancy termination: Medication abortion" and "Misoprostol as a single agent for medical termination of pregnancy".)

Aspiration abortion is most common through 14 weeks of gestation; more advanced gestations usually require initial use of vacuum aspiration followed by use of forceps after cervical dilation (ie, dilation and evacuation [D&E]). (See "First-trimester pregnancy termination: Uterine aspiration".)

Are there contraindications to either approach? – Contraindications to medication (eg, hemoglobin ≤9 g/dL, hemorrhagic disorders) and surgical abortion (eg, fibroid restricting access to the uterine cavity) are discussed separately. (See 'Laboratory testing' above and "First-trimester pregnancy termination: Medication abortion", section on 'Contraindications' and "First-trimester pregnancy termination: Uterine aspiration", section on 'Contraindications'.)

Patient preference – The main factor affecting choice of procedure is patient experience.

Factors favoring medication – Medication abortion allows the patient to avoid a surgical procedure and anesthesia, and some patients feel that the process seems more "natural." Some patients prefer medication abortion because they feel they have a greater degree of control over the process as they manage the procedure privately within their own home [20].

In addition, patients may feel more empowered with telemedicine rather than in-person medication abortion, allowing for increased convenience and privacy [21-27]. Patients with specific socioeconomic or personal concerns (eg, privacy, convenience, limited access to in-person care) may also prefer telemedicine rather in-person medication abortion [19,28].

Factors favoring uterine aspiration – The uterine aspiration procedure takes place at a health care facility, is typically completed in less than 15 minutes, is performed under local anesthesia and/or sedation, and, greater than 99 percent of the time, allows patients to leave the visit knowing that the abortion is complete (see 'Relative outcomes' below). By contrast, medication abortion takes longer, has a slightly lower efficacy, and patients may have a greater awareness of blood loss and passage of pregnancy tissue, particularly at later gestations [29]; for some patients, awareness of these aspects of the process may lead them to choose aspiration abortion.

Some socioeconomic or personal concerns (eg, housing instability, poor social support, upcoming travel) may make uterine aspiration a favored choice due to shorter and more predictable vaginal bleeding compared with medication abortion.

Patients place significant value on the option to choose between medication and aspiration abortion [30]. In studies where patients are allowed a choice between abortion methods, 35 to 84 percent chose medication abortion. Most patients who select medication abortion report they would opt for medication abortion again (63 to 96 percent) if they had another abortion in the future [31]. When looking at choices between in-person and telemedicine abortion, patients who choose a telemedicine medication abortion are more likely to choose telemedicine again [22] or recommend the service to a friend [21] compared with those who had in-person visits [21].

Procedure setting — In general, the site of pregnancy termination depends on the type of termination procedure. Hospitalization may be required for patients with medical conditions that place them at higher risk of medical or surgical complications (eg, cardiac disease, coagulopathy).

Medication abortion – While medication abortion was traditionally a clinic-based service, during the coronavirus disease 2019 (COVID-19) pandemic, when access to medical care was limited, there was an increase in telemedicine and no-test abortion services [32-36]. In a telemedicine or no-test medication abortion, an eligible patient (eg, a patient with a known last menstrual period [LMP], no risk factors for ectopic pregnancy (table 1), no history of hemorrhagic disorders) can receive a medication abortion without receiving in-person care (including a pre- or posttreatment ultrasound, laboratory testing, and physical examination). Counseling and assessment occur via video or phone communication and medications are dispensed by curbside pickup or mail. Hybrid models, where components of the medication abortion visit are completed via telemedicine and other components (eg, picking up medications) in the clinic, also occur. (See "First-trimester pregnancy termination: Medication abortion", section on 'Settings'.)

These models have been shown to be equally safe and effective as the traditional clinic medication abortion model. (See 'Relative outcomes' below.)

Aspiration abortion – Aspiration abortion is typically performed in an outpatient setting, such as in a clinic, a clinician's office equipped with a procedure room, or an ambulatory surgery center, but sometimes occurs in a hospital-based procedure or operating room. (See "First-trimester pregnancy termination: Uterine aspiration", section on 'Procedure setting'.)

Relative outcomes

According to procedure type – Aspiration abortion is slightly more effective than medication abortion as it results in termination of pregnancy in over 99 percent of procedures [37,38]. The success rate of medication abortion with mifepristone and misoprostol is 95 to 98 percent, with 2 to 5 percent of cases requiring further intervention with repeat misoprostol or suction dilation and curettage for retained tissue or continuing pregnancy [39,40]. (See "First-trimester pregnancy termination: Medication abortion", section on 'Complete abortion rates'.)

Overall, complications are more common in medication abortion than in aspiration abortion, driven largely by the need for aspiration to treat retained tissue or ongoing pregnancy [38,41-43]. Representative studies include the following:

In a state-level, insurance claims-based study that captured all emergency department visits following 50,000 abortion procedures, complication rates were higher following medication compared with aspiration abortion [43].

In a retrospective study including 30,146 patients undergoing first-trimester pregnancy termination at a large abortion clinic, the efficacy of pregnancy termination was 99.6 percent for medication abortion (which included cases that required repeat misoprostol or uterine aspiration for initially incomplete procedures) and 99.8 percent for the aspiration abortion group. Patients in the medication abortion group were more likely to undergo an unanticipated aspiration for ongoing pregnancy or persistent pain, bleeding, or both (2.1 compared with 0.6 percent, respectively) [38].

According to procedure setting – Outcomes according to procedure setting (eg, ambulatory surgery center, office-based setting) are similar. In a study including over 50,000 abortions (all types) from a United States private insurance database, the incidence of adverse events was comparable for procedures performed in either an ambulatory surgery center or office-based setting [44].

Large observational studies have also shown that no-test telemedicine abortion is equally effective and safe as clinic-based medication abortion [21,45-55]. In the largest retrospective study including over 52,000 patients undergoing pregnancy termination, patients undergoing telemedicine compared with traditional clinic-based medication abortion had similar rates of adverse outcomes, which were rare [51].

A more detailed discussion of potential complications associated with medication and surgical abortion is provided below. (See 'Complications' below.)

Second trimester — Similar to first-trimester abortion, second-trimester procedures can be performed with induction (medication) or surgery (D&E). How to choose between procedure types, procedure setting (eg, outpatient facility, labor and delivery unit), and the relative outcomes of each are discussed in detail separately. (See "Overview of second-trimester pregnancy termination".)

PREPARATION FOR PROCEDURE

Alloimmunization prevention — RhD-negative patients undergoing pregnancy termination have traditionally received Rh(D) immune globulin to prevent alloimmunization. While this concurs with the approach taken by United States and Canadian guidelines [56,57], not all experts agree, and some clinicians do not administer Rh(D) globulin for gestations that are <56 days (eight weeks) of gestation [14]. This is because the risk for alloimmunization has been shown to be negligible in such patients [14-17]. In other countries, guidelines vary regarding whether Rh(D) immune globulin is required for first-trimester spontaneous abortion. (See 'Laboratory testing' above and "RhD alloimmunization: Prevention in pregnant and postpartum patients".)

When Rh(D) globin is given, a dose of 50 mcg is effective through the 12th week of gestation due to the small volume of red cells in the fetoplacental circulation (mean red cell volume at 8 and 12 weeks is 0.33 and 1.5 mL, respectively), although there is no harm in giving the standard 300 mcg dose, which is more readily available [56,57]. (See "RhD alloimmunization: Prevention in pregnant and postpartum patients", section on 'Anti-D immune globulin'.)

Cervical dilation and preparation — Mechanical dilation of the cervix at the time of surgical aspiration, to allow insertion of instruments and removal of the products of conception, is usually necessary after 8 weeks of gestation and sometimes for earlier gestations. Cervical preparation with osmotic dilators and/or prostaglandins is often used prior to surgical abortions performed after 12 weeks of gestation. This is discussed in detail separately. (See "Pregnancy termination: Cervical preparation for surgical procedures" and "Second-trimester pregnancy termination: Induction (medication) termination", section on 'Cervical preparation'.)

Antibiotic prophylaxis — Use of antibiotic prophylaxis varies by procedure type and other factors; this is discussed in detail separately.

(See "First-trimester pregnancy termination: Medication abortion", section on 'Prophylactic antibiotics'.)

(See "First-trimester pregnancy termination: Uterine aspiration", section on 'Antibiotic prophylaxis'.)

(See "Second-trimester pregnancy termination: Dilation and evacuation", section on 'Prophylactic antibiotics'.)

(See "Second-trimester pregnancy termination: Induction (medication) termination", section on 'Prophylactic antibiotics'.)

Pain management — Pain management varies by procedure type. For example, nonsteroidal anti-inflammatory drugs, with or without oral narcotics, are often used for first-trimester medication abortions, while patients undergoing a second-trimester abortion may receive a paracervical block and intravenous conscious sedation prior to a dilation and evacuation (D&E) or an epidural prior to a medication induction. This is discussed in detail separately.

(See "First-trimester pregnancy termination: Medication abortion", section on 'Abdominal pain'.)

(See "Second-trimester pregnancy termination: Dilation and evacuation", section on 'Anesthesia'.)

(See "Second-trimester pregnancy termination: Induction (medication) termination", section on 'Anesthesia'.)

Guidelines for staff and equipment — The National Abortion Federation (NAF) has issued clinical policy guidelines regarding medical personnel and facilities that provide pregnancy termination care [58]. These stipulate, for example, that abortions should be provided by a licensed practitioner. The minimum requirements for a facility include on-site presence of a medical staff member with updated basic life support certification; an oxygen delivery system, oral airways, self-inflating respirator bags, and bronchodilators; and uterotonics and vasopressors, including epinephrine. In settings in which opioids or benzodiazepines are used, appropriate antagonists must be available.

It is useful for outpatient clinics to have written protocols to address emergencies, particularly indications for emergency transport to a hospital and contact information for personnel who are immediately available to facilitate transport.

FOLLOW-UP — After pregnancy termination, patients may experience vaginal bleeding that is comparable to a menstrual period and that decreases over time; passage of small clots of blood from the vagina may also occur. Patients may experience mild lower abdominal cramping, which can be treated with nonsteroidal anti-inflammatory drugs. The provider should be called for bleeding heavier than a normal period, fever ≥38°C (≥100.4°F), or if more severe abdominal pain develops. Postprocedure care and instructions are provided in writing and reviewed verbally (table 2). Historically, patients have been counseled to avoid vaginal intercourse and use of tampons for two weeks after the procedure to reduce the risk of infection. However, these instructions are not evidence-based and are no longer advised by the authors.

For patients in whom posttermination human chorionic gonadotropin (hCG) levels are followed (eg, products of conception not visible after first-trimester uterine aspiration, patients in whom ectopic pregnancy is a concern), an elevated level of hCG is expected for a short period of time. Return of the serum hCG concentration to undetectable following pregnancy termination varies widely from 7 to 60 days [59]. The duration depends primarily on the hCG concentration at the time of termination. The decline in serum hCG is rapid for the first several days (half-life 9 to 31 hours) and then proceeds more slowly (half-life 55 to 64 hours) [60-62]. (See 'Ectopic pregnancy' below and "Human chorionic gonadotropin: Biochemistry and measurement in pregnancy and disease".)

Specific follow-up details, as they relate to trimester and procedure type, are discussed separately.

(See "First-trimester pregnancy termination: Medication abortion", section on 'Final step: Follow-up and confirmation of complete abortion'.)

(See "First-trimester pregnancy termination: Uterine aspiration", section on 'Recovery and follow-up'.)

(See "Overview of second-trimester pregnancy termination", section on 'Follow-up'.)

COMPLICATIONS

Overall — The rate of complications associated with pregnancy termination depends on the procedure type, gestation, patient characteristics, and clinician experience. In general, the risk of a major complication is low. In a retrospective study of California Medicaid data from 54,911 abortion procedures, the overall complication rate was 2.1 percent [43]. Rates of major (ie, hospital admission, surgery, transfusion) and minor complications were:

First-trimester aspiration – Major 0.16 percent; minor 1.1 percent

Medication abortion – Major 0.31 percent; minor 4.88 percent

Complication rates may be higher in patients with medical conditions. In a study based on national United States inpatient data from 2000 to 2011 including over 38,000,000 patients who underwent a medically necessary abortion (defined as needed to protect a patient's health), the rate of severe maternal morbidity was 62.4 per 10,000 hospitalizations [63].

Hemorrhage — Postabortion hemorrhage occurs in less than 1 percent of abortions [64]. Hemorrhage may result from uterine atony, cervical laceration, uterine perforation, or retained tissue. Other causes of hemorrhage include infection, uterine arteriovenous malformation, placenta accreta spectrum, vaginal laceration, and coagulopathy (secondary to release of tissue thromboplastin into the maternal venous system). Treatment of postabortion hemorrhage is similar to postpartum hemorrhage following vaginal birth. (See "Postpartum hemorrhage: Medical and minimally invasive management".)

The Society of Family Planning guidelines advise the following general approach to postabortion hemorrhage [64]:

Assessment and examination, including repair of bleeding cervical or vaginal lacerations and exploration (and evacuation) of the uterus for retained products of conception.

Treatment of uterine atony with:

Uterine massage and compression. (See "Postpartum hemorrhage: Medical and minimally invasive management", section on 'Perform uterine massage and compression'.)

Uterotonic drugs (ie, oxytocin, methylergonovine maleate, carboprost tromethamine injection [commercial name Hemabate], misoprostol) are discussed in detail separately. (See "Postpartum hemorrhage: Medical and minimally invasive management", section on 'Administer additional uterotonic drugs and consider tamponade'.)

Intrauterine tamponade – When intrauterine tamponade is used, one method is to insert a Foley catheter into the uterine cavity and expand the 30 mL balloon with 50 to 60 mL saline or water. Other types of intrauterine tamponade are discussed in detail separately. (See "Postpartum hemorrhage: Use of intrauterine tamponade to control bleeding", section on 'Types and efficacy of intrauterine tamponade'.)

Laboratory evaluation, including complete blood count and coagulation studies, and resuscitative measures (eg, fluid replacement, oxygenation, transfusion with blood products). (See "Overview of postpartum hemorrhage".)

Pelvic embolization may be used for treatment of hemorrhage if other measures are not successful and the patient is stable [65,66]. Bleeding that continues despite all other measures may require uterine artery ligation or hysterectomy, but this is rare after abortion.

Uterine perforation — Uterine perforation is rare, occurring in fewer than 0.3 percent of first- and second-trimester procedural abortions [64]. Suspected uterine perforation requires further evaluation. The specific location of a uterine perforation determines the symptoms and degree of hemorrhage.

Two factors associated with an increased risk of perforation during pregnancy termination are surgeon inexperience (residents have a 5.5-fold increase in perforations as compared with attending staff) and lack of adequate preoperative cervical dilation [67].

Uterine perforation is discussed in detail separately. (See "Uterine perforation during gynecologic procedures".)

Ongoing pregnancy — Ongoing pregnancy is more likely to be a complication of early rather than late abortion and is more common in patients undergoing medication rather than surgical abortion. It occurs in approximately 0.5 percent of medication (ie, mifepristone plus misoprostol) abortions [42]. (See 'Relative outcomes' above.)

When surgical abortion is performed, products of conception should be closely examined by an experienced clinician to verify successful completion. Although rare, ongoing pregnancy may result from a multiple gestation in which only one of the sacs was removed. (See "First-trimester pregnancy termination: Uterine aspiration", section on 'Tissue evaluation'.)

The type and risk of possible damage to the ongoing pregnancy from an attempted abortion is unclear. Direct or indirect injury to the developing embryo may occur. (See "First-trimester pregnancy termination: Medication abortion", section on 'Teratogenicity' and "Misoprostol as a single agent for medical termination of pregnancy", section on 'Teratogenicity' and "First-trimester pregnancy termination: Uterine aspiration", section on 'Ongoing pregnancy'.)

Infection/retained products of conception — Sepsis after pregnancy termination is rare and is suggested by generalized abdominal tenderness, guarding, tachycardia, and high fever. These patients require aggressive therapy with broad-spectrum intravenous antibiotics, prompt assessment for retained products of conception and removal if present, evaluation for uterine perforation, and monitoring and support in an intensive care unit. (See "Septic abortion: Clinical presentation and management".)

Postabortion endometritis is also uncommon and occurs in <1 percent of patients [68]; this can occur either with or without retained gestational tissue. Signs and symptoms are similar for isolated endometritis and endometritis with retained products of conception and include fever, uterine tenderness, lower abdominal pain, and greater than expected uterine bleeding. Ultrasonography can evaluate for retained products in the uterine cavity. Any physical or sonographic evidence of retained products of conception should prompt consideration of suction curettage to complete evacuation of the uterus. (See "Retained products of conception in the first half of pregnancy".)

In the absence of detectable retained material, a presumptive diagnosis of endometritis may be made and treated with a trial of broad-spectrum antibiotic therapy, with coverage of anaerobes (eg, cefotetan [2 grams intravenously] plus doxycycline [100 mg intravenously or orally] every 12 hours). This regimen can be completed as an outpatient oral regimen for a 14-day course. An alternative outpatient regimen is ceftriaxone 250 mg intramuscularly in a single dose plus doxycycline 100 mg orally twice a day for 14 days with or without metronidazole 500 mg orally twice a day for 14 days.

Maternal mortality — The overall death rate from all legal abortions is far less than the maternal mortality rate among live births in the Unites States (table 3) [69-71]. Maternal mortality is lowest before 9 weeks of gestation and increases rapidly after 18 weeks of gestation (<0.3 per 100,000 induced abortions at <9 weeks versus 7 per 100,000 at 16 to 20 weeks and 11 per 100,000 at ≥21 weeks) [70]. For counseling purposes, this risk of first-trimester pregnancy termination can be compared with other procedures, such as plastic surgery procedures (0.8 to 1.7 deaths per 100,000) or dental procedures (0 to 1.7 deaths per 100,000) [69].

Aspiration abortion has the lowest maternal mortality rate of any surgical pregnancy termination method. One study reported no maternal deaths in 170,000 consecutive first-trimester suction curettage procedures [72].

Countries with better training of and access to abortion providers have lower maternal mortality rates [73]. This relationship is also true in the United States; states that have restricted abortion access have increasing maternal mortality while it is declining in states with improved access to abortion services [6].

SPECIAL CONSIDERATIONS

Unsafe abortion — Access to safe abortion care is an essential component of health care. Unfortunately, a large portion of abortions are considered "unsafe," and these abortions are a major contributor to both maternal morbidity and mortality. The risk of complications and death from unsafe abortion is inversely related to the provider's training [74], skill, conditions for performing the procedure, and availability of appropriate equipment. Some unsafe abortions are self-induced; the consequences in these cases also depend on whether the patient has access to, or can seek, medical care. (See "Unsafe abortion".)

Ectopic pregnancy — Ectopic pregnancy occurs in less than 1 percent of patients presenting for pregnancy termination [75,76]; in the United States, this is approximately three times lower than the national rate of ectopic pregnancy [77]. However, when it does occur, ectopic pregnancy can cause significant maternal morbidity and mortality. For any abortion performed with a pregnancy of unknown location (ie, no yolk sac or fetal pole noted on a pretreatment ultrasound), it is important to evaluate for risk of ectopic pregnancy (table 1). Ectopic pregnancy can be ruled out postabortion by either identifying products of conception after aspiration or by a postabortion serum human chorionic gonadotropin (hCG) level with a sharp decline from a baseline preabortion value. (See 'Follow-up' above and "Ectopic pregnancy: Clinical manifestations and diagnosis".)

Future pregnancies — Data regarding the association of pregnancy termination and subsequent adverse pregnancy outcomes (eg, preterm birth, low birth weight) are conflicting [17,78-87]. Variables that may affect outcomes include study design, gestational age at time of termination, time period of the included studies (which may reflect changes in postabortion or pregnancy care), and procedure type.

Future obstetric outcomes by procedure type are as follows:

Surgical abortion – Surgical abortion may be associated with adverse pregnancy outcomes. In a meta-analysis including 31 studies (>900,000 patients) with a history of surgical termination of pregnancy compared with patients without uterus instrumentation, prior surgical abortion was associated with an increased risk of preterm birth, low birth weight, and small for gestational age (SGA) infants, although the absolute risk remained small [82]. The reported outcomes were: preterm birth, 5.4 versus 4.4 percent, odds ratio (OR) 1.52, 95% CI 1.08-2.16; low birth weight, 7.3 versus 5.9 percent, OR 1.41, 95% CI 1.22-1.62; and SGA, 10.2 versus 9 percent, OR 1.19, 95% CI 1.01-1.42. (See "Preterm birth: Risk factors, interventions for risk reduction, and maternal prognosis", section on 'History of abortion'.)

By contrast, other series addressing future pregnancy in patients who underwent a prior surgical abortion do not show this association [78,83,84,88]. In a retrospective review including 600 patients undergoing dilation and evacuation (D&E) between 14 and 24 weeks, the overall rate of preterm birth in subsequent pregnancies was less than the overall rate of preterm birth for the general United States population (6.5 versus 12.5 percent) [83]. Similarly, in a study that compared subsequent pregnancy outcomes among 317 patients with a history of second-trimester D&E and 170 matched controls, patients with a history of prior D&E delivered slightly earlier in gestation than controls (38.9 versus 39.5 weeks of gestation), but birth weight, spontaneous preterm delivery, abnormal placentation, and overall rates of perinatal complications were similar between groups [88].

Medication abortion – Several studies have reported similar risk of adverse obstetric outcomes among patients with medication abortion compared with no uterus instrumentation or surgical abortion [82,85].

Rates of complications were also similar among patients undergoing medication or surgical abortion in a retrospective study including over 8000 primigravid patients [85]. In this study, patients who had previously undergone either medication or surgical abortion had similar rates of preterm birth, low birth weight, SGA infants, or placental complications in subsequent singleton pregnancies. By contrast, in a retrospective including 173 patients undergoing second-trimester termination for fetal indications, patients with a prior medication termination (43 patients) compared with D&E (130 patients) had higher rates of subsequent preterm birth (30.2 versus 6.9 percent), but the overall number of events was low [89].

Patients undergoing medication termination in the first compared with second trimester appear to have similar risk pregnancy outcomes. In a retrospective study including 88,000 primigravid patients undergoing medication termination of pregnancy followed by a subsequent live birth, patients who had the procedure in the first compared with second trimester had similar risks of preterm birth, low birth weight, SGA infants, and placental complications [86].

The association between induced abortion and subsequent placental problems has also been studied. A report of all primigravid patients delivering in Denmark from 1980 to 1982 used data from the Danish Birth, Hospital Discharge, and Induced Abortion Registries to compare the risk of placental complications in subsequent pregnancy among 15,727 patients who underwent first-trimester termination and 46,026 patients who did not have a termination [90]; patients were followed for 12 years. There was no difference in the risk of placenta previa, but patients with a previous termination had a slightly higher rate of retained placenta (OR 1.17, 95% CI 1.02-1.35).

Breast cancer — Pregnancy termination does not appear to be associated with an increased risk of breast cancer, although data are conflicting. A United States National Cancer Institute meta-analysis included individual data from 53 studies (83,000 females) in 16 countries and reported that the risk of breast cancer was not increased in those with a history of induced abortion (relative risk [RR] 0.93, 95% CI 0.89-0.96) [91]. Other published studies have confirmed this conclusion [92-95]. By contrast, a meta-analysis of 36 comparative studies in China found that a history of induced abortion was associated with an increase in the risk of breast cancer (OR 1.44, 95% CI 1.29-1.59) [96].

Ongoing health — Pregnancy termination does not appear be associated with ongoing health issues. In a prospective study including 874 patients with undesired pregnancy, more patients who continued the pregnancy to birth reported fair to poor health compared with patients who underwent first- or second-trimester termination (27 versus 20 and 21 percent, respectively) [97]. Self-rated health and chronic pain outcomes were similar between the first- and second-trimester abortion groups at five years.

In addition, while patients may experience a variety of short- and long-term emotions, the predominant feeling reported is relief [98]. A detailed discussion about the effects of abortion on mental health are discussed elsewhere. (See "Pregnancy termination and potential psychiatric outcomes".)

SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Pregnancy termination".)

INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.)

Basics topic (see "Patient education: Abortion (The Basics)")

Beyond the Basics topic (see "Patient education: Abortion (pregnancy termination) (Beyond the Basics)")

SUMMARY AND RECOMMENDATIONS

General issues pertaining to pregnancy termination

Counseling – Counseling should include a nondirective discussion of alternatives (ie, continuing pregnancy with parenting or adoption) and a thorough discussion of the medical and surgical options for pregnancy termination, including the risks, benefits, and expected outcome of each. (See 'Counseling and informed consent' above.)

Determining gestational age – Determining the correct gestational age with menstrual dating (with or without bimanual examination) or ultrasound evaluation is a critical part of preabortion care. Menstrual dating should only be used in patients in whom the date of the last menstrual period (LMP) is known with certainty and in those with regular menstrual cycles. We perform a preprocedural ultrasound prior to all second-trimester abortions.

Contraception – Ovulation can occur soon after an abortion and before the onset of menses; thus, offering immediate contraception is important and can be generally initiated the day of the procedure, if desired. (See 'Plan for contraception' above.)

Alloimmunization prevention – RhD status should be determined if the gestational age is ≥56 days. RhD-negative patients should receive anti-D immune globulin after their treatment. (See 'Laboratory testing' above and 'Alloimmunization prevention' above.)

Cervical dilation and preparation – Mechanical cervical dilation before uterine aspiration is generally required after 8 weeks of gestation (and sometimes before). Cervical preparation with osmotic dilators and/or prostaglandins is generally necessary after 12 weeks of gestation to dilate the cervix more slowly before dilation and evacuation (D&E). (See 'Cervical dilation and preparation' above.)

Follow-up – Follow-up depends on the gestational age at which the termination is performed and procedure type. An example of postprocedure care instructions is shown in the table (table 2).

Complications – Potential complications include hemorrhage, uterine perforation, infection, missed ectopic pregnancy, ongoing pregnancy, and retained products of conception. The overall risk of major complication (ie, hospital admission, surgery, transfusion) is low. (See 'Complications' above and 'Ectopic pregnancy' above.)

Choice of procedure

First-trimester termination – For patients undergoing termination at <77 days (11 weeks) of gestation, either medication or surgical abortion are appropriate options. The choice between traditional clinic-based medication abortion, no-test or telemedicine medication abortion, and aspiration is based upon gestational age, eligibility, availability, and patient preference. Patients who place value on avoiding surgery or anesthesia and who are willing to accept more discomfort and awareness of blood and tissue loss may opt for a medication abortion. Patients who place a high value on completing the procedure in one visit are more likely to choose aspiration abortion. Eligible patients (eg, known LMP, no risk factors for ectopic pregnancy (table 1), no history of hemorrhagic disorders) who desire medication abortion may opt for telemedicine abortion. (See 'First trimester' above.)

Second-trimester termination – Similar to first-trimester abortion, second-trimester procedures can be performed with induction (medication) or surgery (D&E). How to choose between procedure types, procedure setting (eg, outpatient facility, labor and delivery unit), and the relative outcomes of medication and surgical termination in the second trimester are discussed in detail separately. (See 'Second trimester' above and "Overview of second-trimester pregnancy termination", section on 'Choosing dilation and evacuation versus induction termination'.)

ACKNOWLEDGMENT — The UpToDate editorial staff acknowledges Lee P Shulman, MD, and Frank W Ling, MD, who contributed to earlier versions of this topic review.

REFERENCES

  1. Sedgh G, Bearak J, Singh S, et al. Abortion incidence between 1990 and 2014: global, regional, and subregional levels and trends. Lancet 2016; 388:258.
  2. Jones RK, Jerman J. Abortion Incidence and Service Availability In the United States, 2014. Perspect Sex Reprod Health 2017; 49:17.
  3. Kortsmit K, Jatlaoui TC, Mandel MG, et al. Abortion Surveillance - United States, 2018. MMWR Surveill Summ 2020; 69:1.
  4. Thompson KMJ, Sturrock HJW, Foster DG, Upadhyay UD. Association of Travel Distance to Nearest Abortion Facility With Rates of Abortion. JAMA Netw Open 2021; 4:e2115530.
  5. Parental Consent and Notification Laws. Planned Parenthood. Available at: https://www.plannedparenthood.org/learn/teens/stds-birth-control-pregnancy/parental-consent-and-notification-laws (Accessed on September 21, 2021).
  6. Addante AN, Eisenberg DL, Valentine MC, et al. The association between state-level abortion restrictions and maternal mortality in the United States, 1995-2017. Contraception 2021; 104:496.
  7. Questions and Answers on Mifeprex. US Food and Drug Administration. Available at: https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-and-providers/questions-and-answers-mifeprex (Accessed on January 07, 2022).
  8. Schummers L, Darling EK, Dunn S, et al. Abortion Safety and Use with Normally Prescribed Mifepristone in Canada. N Engl J Med 2022; 386:57.
  9. Schonberg D, Wang LF, Bennett AH, et al. The accuracy of using last menstrual period to determine gestational age for first trimester medication abortion: a systematic review. Contraception 2014; 90:480.
  10. Raymond EG, Bracken H. Early medical abortion without prior ultrasound. Contraception 2015; 92:212.
  11. Bracken H, Clark W, Lichtenberg ES, et al. Alternatives to routine ultrasound for eligibility assessment prior to early termination of pregnancy with mifepristone-misoprostol. BJOG 2011; 118:17.
  12. 2015 Clinical Policy Guidelines. National Abortion Federation. Available at: http://prochoice.org/wp-content/uploads/2015_NAF_CPGs.pdf (Accessed on October 15, 2015).
  13. American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Gynecology, Society of Family Planning. Medication Abortion Up to 70 Days of Gestation: ACOG Practice Bulletin, Number 225. Obstet Gynecol 2020; 136:e31.
  14. Mark A, Foster AM, Grossman D, et al. Foregoing Rh testing and anti-D immunoglobulin for women presenting for early abortion: a recommendation from the National Abortion Federation's Clinical Policies Committee. Contraception 2019; 99:265.
  15. Hollenbach SJ, Cochran M, Harrington A. "Provoked" feto-maternal hemorrhage may represent insensible cell exchange in pregnancies from 6 to 22 weeks gestational age. Contraception 2019; 100:142.
  16. Horvath S, Luning Prak ET, Schreiber CA. A highly sensitive flow cytometry protocol shows fetal red blood cell counts in first-trimester maternal circulation well below the threshold for Rh sensitization. Contraception 2018; 98:332.
  17. Abortion care guideline. National Institute for Health and Care Excellence 2019. Available at: https://www.nice.org.uk/guidance/ng140 (Accessed on July 23, 2021).
  18. Mifeprex (mifepristone) Information. US Food and Drug Administration. Available at: http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm111323.htm (Accessed on March 30, 2016).
  19. Clinical policy guidelines for abortion care. National Abortion Federation 2020. Available at: https://prochoice.org/store/clinical-policy-guidelines/ (Accessed on July 23, 2021).
  20. Robson SC, Kelly T, Howel D, et al. Randomised preference trial of medical versus surgical termination of pregnancy less than 14 weeks' gestation (TOPS). Health Technol Assess 2009; 13:1.
  21. Grossman D, Grindlay K, Buchacker T, et al. Effectiveness and acceptability of medical abortion provided through telemedicine. Obstet Gynecol 2011; 118:296.
  22. Porter Erlank C, Lord J, Church K. Acceptability of no-test medical abortion provided via telemedicine during Covid-19: analysis of patient-reported outcomes. BMJ Sex Reprod Health 2021; 47:261.
  23. Fix L, Seymour JW, Sandhu MV, et al. At-home telemedicine for medical abortion in Australia: a qualitative study of patient experiences and recommendations. BMJ Sex Reprod Health 2020; 46:172.
  24. Grossman DA, Grindlay K, Buchacker T, et al. Changes in service delivery patterns after introduction of telemedicine provision of medical abortion in Iowa. Am J Public Health 2013; 103:73.
  25. Ehrenreich K, Marston C. Spatial dimensions of telemedicine and abortion access: a qualitative study of women's experiences. Reprod Health 2019; 16:94.
  26. Grindlay K, Lane K, Grossman D. Women's and providers' experiences with medical abortion provided through telemedicine: a qualitative study. Womens Health Issues 2013; 23:e117.
  27. Ehrenreich K, Kaller S, Raifman S, Grossman D. Women's Experiences Using Telemedicine to Attend Abortion Information Visits in Utah: A Qualitative Study. Womens Health Issues 2019; 29:407.
  28. Medication Abortion Up to 70 Days of Gestation: ACOG Practice Bulletin Summary, Number 225. Obstet Gynecol 2020; 136:855.
  29. Winikoff B, Dzuba IG, Chong E, et al. Extending outpatient medical abortion services through 70 days of gestational age. Obstet Gynecol 2012; 120:1070.
  30. Moreau C, Trussell J, Desfreres J, Bajos N. Medical vs. surgical abortion: the importance of women's choice. Contraception 2011; 84:224.
  31. Costescu D, Guilbert E, Bernardin J, et al. Medical Abortion. J Obstet Gynaecol Can 2016; 38:366.
  32. Bayefsky MJ, Bartz D, Watson KL. Abortion during the Covid-19 Pandemic - Ensuring Access to an Essential Health Service. N Engl J Med 2020; 382:e47.
  33. Raymond EG, Grossman D, Mark A, et al. Commentary: No-test medication abortion: A sample protocol for increasing access during a pandemic and beyond. Contraception 2020; 101:361.
  34. Roberts SC, Schroeder R, Joffe C. COVID-19 and Independent Abortion Providers: Findings from a Rapid-Response Survey. Perspect Sex Reprod Health 2020; 52:217.
  35. Sackeim MG. Protecting Access To Abortion During The COVID-19 Pandemic. Health Aff (Millwood) 2020; 39:1456.
  36. Joint statement on abortion access during the COVID-19 outbreak. The American College of Gynecologists (ACOG) 2020. https://www.acog.org/news/news-releases/2020/03/joint-statement-on-abortion-access-during-the-covid-19-outbreak (Accessed on July 23, 2021).
  37. Ngo TD, Park MH, Free C. Safety and effectiveness of termination services performed by doctors versus midlevel providers: a systematic review and analysis. Int J Womens Health 2013; 5:9.
  38. Ireland LD, Gatter M, Chen AY. Medical Compared With Surgical Abortion for Effective Pregnancy Termination in the First Trimester. Obstet Gynecol 2015; 126:22.
  39. Jensen JT, Astley SJ, Morgan E, Nichols MD. Outcomes of suction curettage and mifepristone abortion in the United States. A prospective comparison study. Contraception 1999; 59:153.
  40. Gatter M, Cleland K, Nucatola DL. Efficacy and safety of medical abortion using mifepristone and buccal misoprostol through 63 days. Contraception 2015; 91:269.
  41. Chen MJ, Creinin MD. Mifepristone With Buccal Misoprostol for Medical Abortion: A Systematic Review. Obstet Gynecol 2015; 126:12.
  42. Cleland K, Creinin MD, Nucatola D, et al. Significant adverse events and outcomes after medical abortion. Obstet Gynecol 2013; 121:166.
  43. Upadhyay UD, Desai S, Zlidar V, et al. Incidence of emergency department visits and complications after abortion. Obstet Gynecol 2015; 125:175.
  44. Roberts SC, Upadhyay UD, Liu G, et al. Association of Facility Type With Procedural-Related Morbidities and Adverse Events Among Patients Undergoing Induced Abortions. JAMA 2018; 319:2497.
  45. Hyland P, Raymond EG, Chong E. A direct-to-patient telemedicine abortion service in Australia: Retrospective analysis of the first 18 months. Aust N Z J Obstet Gynaecol 2018; 58:335.
  46. Gambir K, Garnsey C, Necastro KA, Ngo TD. Effectiveness, safety and acceptability of medical abortion at home versus in the clinic: a systematic review and meta-analysis in response to COVID-19. BMJ Glob Health 2020; 5.
  47. Kohn JE, Snow JL, Simons HR, et al. Medication Abortion Provided Through Telemedicine in Four U.S. States. Obstet Gynecol 2019; 134:343.
  48. Grossman D, Grindlay K. Safety of Medical Abortion Provided Through Telemedicine Compared With In Person. Obstet Gynecol 2017; 130:778.
  49. Raymond E, Chong E, Winikoff B, et al. TelAbortion: evaluation of a direct to patient telemedicine abortion service in the United States. Contraception 2019; 100:173.
  50. Endler M, Lavelanet A, Cleeve A, et al. Telemedicine for medical abortion: a systematic review. BJOG 2019; 126:1094.
  51. Aiken A, Lohr PA, Lord J, et al. Effectiveness, safety and acceptability of no-test medical abortion (termination of pregnancy) provided via telemedicine: a national cohort study. BJOG 2021; 128:1464.
  52. Reynolds-Wright JJ, Johnstone A, McCabe K, et al. Telemedicine medical abortion at home under 12 weeks' gestation: a prospective observational cohort study during the COVID-19 pandemic. BMJ Sex Reprod Health 2021; 47:246.
  53. Gomperts RJ, Jelinska K, Davies S, et al. Using telemedicine for termination of pregnancy with mifepristone and misoprostol in settings where there is no access to safe services. BJOG 2008; 115:1171.
  54. Aiken AR, Digol I, Trussell J, Gomperts R. Self reported outcomes and adverse events after medical abortion through online telemedicine: population based study in the Republic of Ireland and Northern Ireland. BMJ 2017; 357:j2011.
  55. Kerestes C, Murayama S, Tyson J, et al. Provision of medication abortion in Hawai'i during COVID-19: Practical experience with multiple care delivery models. Contraception 2021; 104:49.
  56. Practice Bulletin No. 181: Prevention of Rh D Alloimmunization. Obstet Gynecol 2017; 130:e57.
  57. Fung KFK, Eason E. No. 133-Prevention of Rh Alloimmunization. J Obstet Gynaecol Can 2018; 40:e1.
  58. 2013 Clinical Policy Guidelines. National Abortion Federation. Available at: https://www.prochoice.org/wp-content/uploads/2013NAFCPGsforweb.pdf (Accessed on June 03, 2013).
  59. Steier JA, Bergsjø P, Myking OL. Human chorionic gonadotropin in maternal plasma after induced abortion, spontaneous abortion, and removed ectopic pregnancy. Obstet Gynecol 1984; 64:391.
  60. Billieux MH, Petignat P, Anguenot JL, et al. Early and late half-life of human chorionic gonadotropin as a predictor of persistent trophoblast after laparoscopic conservative surgery for tubal pregnancy. Acta Obstet Gynecol Scand 2003; 82:550.
  61. Mock P, Chardonnens D, Stamm P, et al. The apparent late half-life of human chorionic gonadotropin (hCG) after surgical treatment for ectopic pregnancy. A new approach to diagnose persistent trophoblastic activity. Eur J Obstet Gynecol Reprod Biol 1998; 78:99.
  62. Midgley AR Jr, Jaffe RB. Regulation of human gonadotropins. II. Disappearance of human chorionic gonadotropin following delivery. J Clin Endocrinol Metab 1968; 28:1712.
  63. Jarlenski M, Hutcheon JA, Bodnar LM, Simhan HN. State Medicaid Coverage of Medically Necessary Abortions and Severe Maternal Morbidity and Maternal Mortality. Obstet Gynecol 2017; 129:786.
  64. Kerns J, Steinauer J. Management of postabortion hemorrhage: release date November 2012 SFP Guideline #20131. Contraception 2013; 87:331.
  65. Borgatta L, Chen AY, Reid SK, et al. Pelvic embolization for treatment of hemorrhage related to spontaneous and induced abortion. Am J Obstet Gynecol 2001; 185:530.
  66. Steinauer JE, Diedrich JT, Wilson MW, et al. Uterine artery embolization in postabortion hemorrhage. Obstet Gynecol 2008; 111:881.
  67. Grimes DA, Schulz KF, Cates WJ Jr. Prevention of uterine perforation during curettage abortion. JAMA 1984; 251:2108.
  68. Achilles SL, Reeves MF, Society of Family Planning. Prevention of infection after induced abortion: release date October 2010: SFP guideline 20102. Contraception 2011; 83:295.
  69. Raymond EG, Grossman D, Weaver MA, et al. Mortality of induced abortion, other outpatient surgical procedures and common activities in the United States. Contraception 2014; 90:476.
  70. Bartlett LA, Berg CJ, Shulman HB, et al. Risk factors for legal induced abortion-related mortality in the United States. Obstet Gynecol 2004; 103:729.
  71. Raymond EG, Grimes DA. The comparative safety of legal induced abortion and childbirth in the United States. Obstet Gynecol 2012; 119:215.
  72. Hakim-Elahi E, Tovell HM, Burnhill MS. Complications of first-trimester abortion: a report of 170,000 cases. Obstet Gynecol 1990; 76:129.
  73. Darney PD, Nakamura-Pereira M, Regan L, et al. Maternal Mortality in the United States Compared With Ethiopia, Nepal, Brazil, and the United Kingdom: Contrasts in Reproductive Health Policies. Obstet Gynecol 2020; 135:1362.
  74. Advancing Women’s Health through Medical Education: A Systems Approach in Family planning and Abortion, Landy U, Darney P, Steinauer J (Eds), Cambridge University Press, 2021. p.371.
  75. Ulmann A, Silvestre L, Chemama L, et al. Medical termination of early pregnancy with mifepristone (RU 486) followed by a prostaglandin analogue. Study in 16,369 women. Acta Obstet Gynecol Scand 1992; 71:278.
  76. Edwards J, Carson SA. New technologies permit safe abortion at less than six weeks' gestation and provide timely detection of ectopic gestation. Am J Obstet Gynecol 1997; 176:1101.
  77. Centers for Disease Control (CDC). Ectopic pregnancy--United States, 1988-1989. MMWR Morb Mortal Wkly Rep 1992; 41:591.
  78. Hogue CJ, Cates W Jr, Tietze C. Impact of vacuum aspiration abortion on future childbearing: a review. Fam Plann Perspect 1983; 15:119.
  79. Hogue CJ, Cates W Jr, Tietze C. The effects of induced abortion on subsequent reproduction. Epidemiol Rev 1982; 4:66.
  80. Atrash HK, Hogue CJ. The effect of pregnancy termination on future reproduction. Baillieres Clin Obstet Gynaecol 1990; 4:391.
  81. Shah PS, Zao J, Knowledge Synthesis Group of Determinants of preterm/LBW births. Induced termination of pregnancy and low birthweight and preterm birth: a systematic review and meta-analyses. BJOG 2009; 116:1425.
  82. Saccone G, Perriera L, Berghella V. Prior uterine evacuation of pregnancy as independent risk factor for preterm birth: a systematic review and metaanalysis. Am J Obstet Gynecol 2016; 214:572.
  83. Kalish RB, Chasen ST, Rosenzweig LB, et al. Impact of midtrimester dilation and evacuation on subsequent pregnancy outcome. Am J Obstet Gynecol 2002; 187:882.
  84. Schneider D, Halperin R, Langer R, et al. Abortion at 18-22 weeks by laminaria dilation and evacuation. Obstet Gynecol 1996; 88:412.
  85. Männistö J, Mentula M, Bloigu A, et al. Medical versus surgical termination of pregnancy in primigravid women--is the next delivery differently at risk? A population-based register study. BJOG 2013; 120:331.
  86. Männistö J, Mentula M, Bloigu A, et al. Medical termination of pregnancy during the second versus the first trimester and its effects on subsequent pregnancy. Contraception 2014; 89:109.
  87. Medical management of abortion. Geneva: World Health Organization; 2018. https://apps.who.int/iris/bitstream/handle/10665/278968/9789241550406-eng.pdf?ua=1 (Accessed on March 03, 2021).
  88. Jackson JE, Grobman WA, Haney E, Casele H. Mid-trimester dilation and evacuation with laminaria does not increase the risk for severe subsequent pregnancy complications. Int J Gynaecol Obstet 2007; 96:12.
  89. Little SE, Janiak E, Bartz D, Smith NA. Second trimester dilation and evacuation: a risk factor for preterm birth? J Perinatol 2015; 35:1006.
  90. Zhou W, Nielsen GL, Larsen H, Olsen J. Induced abortion and placenta complications in the subsequent pregnancy. Acta Obstet Gynecol Scand 2001; 80:1115.
  91. Beral V, Bull D, Doll R, et al. Breast cancer and abortion: collaborative reanalysis of data from 53 epidemiological studies, including 83?000 women with breast cancer from 16 countries. Lancet 2004; 363:1007.
  92. Michels KB, Xue F, Colditz GA, Willett WC. Induced and spontaneous abortion and incidence of breast cancer among young women: a prospective cohort study. Arch Intern Med 2007; 167:814.
  93. Reeves GK, Kan SW, Key T, et al. Breast cancer risk in relation to abortion: Results from the EPIC study. Int J Cancer 2006; 119:1741.
  94. Friedman E, Kotsopoulos J, Lubinski J, et al. Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers. Breast Cancer Res 2006; 8:R15.
  95. Committee on Gynecologic Practice. ACOG Committee Opinion No. 434: induced abortion and breast cancer risk. Obstet Gynecol 2009; 113:1417. Reaffirmed 2021.
  96. Huang Y, Zhang X, Li W, et al. A meta-analysis of the association between induced abortion and breast cancer risk among Chinese females. Cancer Causes Control 2014; 25:227.
  97. Ralph LJ, Schwarz EB, Grossman D, Foster DG. Self-reported Physical Health of Women Who Did and Did Not Terminate Pregnancy After Seeking Abortion Services: A Cohort Study. Ann Intern Med 2019; 171:238.
  98. Rocca CH, Kimport K, Roberts SC, et al. Decision Rightness and Emotional Responses to Abortion in the United States: A Longitudinal Study. PLoS One 2015; 10:e0128832.
Topic 3313 Version 46.0

References

1 : Abortion incidence between 1990 and 2014: global, regional, and subregional levels and trends.

2 : Abortion Incidence and Service Availability In the United States, 2014.

3 : Abortion Surveillance - United States, 2018.

4 : Association of Travel Distance to Nearest Abortion Facility With Rates of Abortion.

5 : Association of Travel Distance to Nearest Abortion Facility With Rates of Abortion.

6 : The association between state-level abortion restrictions and maternal mortality in the United States, 1995-2017.

7 : The association between state-level abortion restrictions and maternal mortality in the United States, 1995-2017.

8 : Abortion Safety and Use with Normally Prescribed Mifepristone in Canada.

9 : The accuracy of using last menstrual period to determine gestational age for first trimester medication abortion: a systematic review.

10 : Early medical abortion without prior ultrasound.

11 : Alternatives to routine ultrasound for eligibility assessment prior to early termination of pregnancy with mifepristone-misoprostol.

12 : Alternatives to routine ultrasound for eligibility assessment prior to early termination of pregnancy with mifepristone-misoprostol.

13 : Medication Abortion Up to 70 Days of Gestation: ACOG Practice Bulletin, Number 225.

14 : Foregoing Rh testing and anti-D immunoglobulin for women presenting for early abortion: a recommendation from the National Abortion Federation's Clinical Policies Committee.

15 : "Provoked" feto-maternal hemorrhage may represent insensible cell exchange in pregnancies from 6 to 22 weeks gestational age.

16 : A highly sensitive flow cytometry protocol shows fetal red blood cell counts in first-trimester maternal circulation well below the threshold for Rh sensitization

17 : A highly sensitive flow cytometry protocol shows fetal red blood cell counts in first-trimester maternal circulation well below the threshold for Rh sensitization

18 : A highly sensitive flow cytometry protocol shows fetal red blood cell counts in first-trimester maternal circulation well below the threshold for Rh sensitization

19 : A highly sensitive flow cytometry protocol shows fetal red blood cell counts in first-trimester maternal circulation well below the threshold for Rh sensitization

20 : Randomised preference trial of medical versus surgical termination of pregnancy less than 14 weeks' gestation (TOPS).

21 : Effectiveness and acceptability of medical abortion provided through telemedicine.

22 : Acceptability of no-test medical abortion provided via telemedicine during Covid-19: analysis of patient-reported outcomes.

23 : At-home telemedicine for medical abortion in Australia: a qualitative study of patient experiences and recommendations.

24 : Changes in service delivery patterns after introduction of telemedicine provision of medical abortion in Iowa.

25 : Spatial dimensions of telemedicine and abortion access: a qualitative study of women's experiences.

26 : Women's and providers' experiences with medical abortion provided through telemedicine: a qualitative study.

27 : Women's Experiences Using Telemedicine to Attend Abortion Information Visits in Utah: A Qualitative Study.

28 : Medication Abortion Up to 70 Days of Gestation: ACOG Practice Bulletin Summary, Number 225.

29 : Extending outpatient medical abortion services through 70 days of gestational age.

30 : Medical vs. surgical abortion: the importance of women's choice.

31 : Medical Abortion.

32 : Abortion during the Covid-19 Pandemic - Ensuring Access to an Essential Health Service.

33 : Commentary: No-test medication abortion: A sample protocol for increasing access during a pandemic and beyond.

34 : COVID-19 and Independent Abortion Providers: Findings from a Rapid-Response Survey.

35 : Protecting Access To Abortion During The COVID-19 Pandemic.

36 : Protecting Access To Abortion During The COVID-19 Pandemic.

37 : Safety and effectiveness of termination services performed by doctors versus midlevel providers: a systematic review and analysis.

38 : Medical Compared With Surgical Abortion for Effective Pregnancy Termination in the First Trimester.

39 : Outcomes of suction curettage and mifepristone abortion in the United States. A prospective comparison study.

40 : Efficacy and safety of medical abortion using mifepristone and buccal misoprostol through 63 days.

41 : Mifepristone With Buccal Misoprostol for Medical Abortion: A Systematic Review.

42 : Significant adverse events and outcomes after medical abortion.

43 : Incidence of emergency department visits and complications after abortion.

44 : Association of Facility Type With Procedural-Related Morbidities and Adverse Events Among Patients Undergoing Induced Abortions.

45 : A direct-to-patient telemedicine abortion service in Australia: Retrospective analysis of the first 18 months.

46 : Effectiveness, safety and acceptability of medical abortion at home versus in the clinic: a systematic review and meta-analysis in response to COVID-19.

47 : Medication Abortion Provided Through Telemedicine in Four U.S. States.

48 : Safety of Medical Abortion Provided Through Telemedicine Compared With In Person.

49 : TelAbortion: evaluation of a direct to patient telemedicine abortion service in the United States.

50 : Telemedicine for medical abortion: a systematic review.

51 : Effectiveness, safety and acceptability of no-test medical abortion (termination of pregnancy) provided via telemedicine: a national cohort study.

52 : Telemedicine medical abortion at home under 12 weeks' gestation: a prospective observational cohort study during the COVID-19 pandemic.

53 : Using telemedicine for termination of pregnancy with mifepristone and misoprostol in settings where there is no access to safe services.

54 : Self reported outcomes and adverse events after medical abortion through online telemedicine: population based study in the Republic of Ireland and Northern Ireland.

55 : Provision of medication abortion in Hawai'i during COVID-19: Practical experience with multiple care delivery models.

56 : Practice Bulletin No. 181: Prevention of Rh D Alloimmunization.

57 : No. 133-Prevention of Rh Alloimmunization.

58 : No. 133-Prevention of Rh Alloimmunization.

59 : Human chorionic gonadotropin in maternal plasma after induced abortion, spontaneous abortion, and removed ectopic pregnancy.

60 : Early and late half-life of human chorionic gonadotropin as a predictor of persistent trophoblast after laparoscopic conservative surgery for tubal pregnancy.

61 : The apparent late half-life of human chorionic gonadotropin (hCG) after surgical treatment for ectopic pregnancy. A new approach to diagnose persistent trophoblastic activity.

62 : Regulation of human gonadotropins. II. Disappearance of human chorionic gonadotropin following delivery.

63 : State Medicaid Coverage of Medically Necessary Abortions and Severe Maternal Morbidity and Maternal Mortality.

64 : Management of postabortion hemorrhage: release date November 2012 SFP Guideline #20131.

65 : Pelvic embolization for treatment of hemorrhage related to spontaneous and induced abortion.

66 : Uterine artery embolization in postabortion hemorrhage.

67 : Prevention of uterine perforation during curettage abortion.

68 : Prevention of infection after induced abortion: release date October 2010: SFP guideline 20102.

69 : Mortality of induced abortion, other outpatient surgical procedures and common activities in the United States.

70 : Risk factors for legal induced abortion-related mortality in the United States.

71 : The comparative safety of legal induced abortion and childbirth in the United States.

72 : Complications of first-trimester abortion: a report of 170,000 cases.

73 : Maternal Mortality in the United States Compared With Ethiopia, Nepal, Brazil, and the United Kingdom: Contrasts in Reproductive Health Policies.

74 : Maternal Mortality in the United States Compared With Ethiopia, Nepal, Brazil, and the United Kingdom: Contrasts in Reproductive Health Policies.

75 : Medical termination of early pregnancy with mifepristone (RU 486) followed by a prostaglandin analogue. Study in 16,369 women.

76 : New technologies permit safe abortion at less than six weeks' gestation and provide timely detection of ectopic gestation.

77 : Ectopic pregnancy--United States, 1988-1989.

78 : Impact of vacuum aspiration abortion on future childbearing: a review.

79 : The effects of induced abortion on subsequent reproduction.

80 : The effect of pregnancy termination on future reproduction.

81 : Induced termination of pregnancy and low birthweight and preterm birth: a systematic review and meta-analyses.

82 : Prior uterine evacuation of pregnancy as independent risk factor for preterm birth: a systematic review and metaanalysis.

83 : Impact of midtrimester dilation and evacuation on subsequent pregnancy outcome.

84 : Abortion at 18-22 weeks by laminaria dilation and evacuation.

85 : Medical versus surgical termination of pregnancy in primigravid women--is the next delivery differently at risk? A population-based register study.

86 : Medical termination of pregnancy during the second versus the first trimester and its effects on subsequent pregnancy.

87 : Medical termination of pregnancy during the second versus the first trimester and its effects on subsequent pregnancy.

88 : Mid-trimester dilation and evacuation with laminaria does not increase the risk for severe subsequent pregnancy complications.

89 : Second trimester dilation and evacuation: a risk factor for preterm birth?

90 : Induced abortion and placenta complications in the subsequent pregnancy.

91 : Breast cancer and abortion: collaborative reanalysis of data from 53 epidemiological studies, including 83?000 women with breast cancer from 16 countries.

92 : Induced and spontaneous abortion and incidence of breast cancer among young women: a prospective cohort study.

93 : Breast cancer risk in relation to abortion: Results from the EPIC study.

94 : Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers.

95 : ACOG Committee Opinion No. 434: induced abortion and breast cancer risk.

96 : A meta-analysis of the association between induced abortion and breast cancer risk among Chinese females.

97 : Self-reported Physical Health of Women Who Did and Did Not Terminate Pregnancy After Seeking Abortion Services: A Cohort Study.

98 : Decision Rightness and Emotional Responses to Abortion in the United States: A Longitudinal Study.