Complications of Surgical Abortions

Introduction


Approximately one-half of all pregnancies in the United States are unintended. One of every two women between the ages of 15–44 will experience an unintended pregnancy. Over 40% of all unintended pregnancies end in abortion, making this one of the most common surgical procedures in this country. Nine out of 10 abortions occur before the end of the first trimester.


Multiple advances in technology over the last two decades have significantly improved the safety and ease of surgical abortion. Transvaginal ultrasonography has replaced assessments of uterine size with objective methods to accurately establish gestational age. Effective techniques have evolved for preoperative cervical preparation. Present-day procedures utilize medical abortifacients alone or in addition to osmotic dilators, to soften and dilate the cervix. Finally, the development of the manual vacuum aspirator, a portable nonelectric uterine evacuation device, for use in early pregnancy termination has not only improved the safety of the procedure, but also expanded accessibility in outpatient settings.


As a result of these developments, complications due to surgical abortion are uncommon. Although the complication rate increases slightly with advancing gestational age, the risk of serious morbidity or mortality is far lower than that associated with carrying a pregnancy to term. Overall mortality from first-trimester abortion in the United States is 1 per 100,000 procedures. The National Abortion Federation states that the overall complication rate in first-trimester terminations is 9 per 1000 procedures. The risk of second-trimester complications rate is more elusive: Stubblefield noted nine perforations per 10,000 procedures with a range of 0.9–21 per 10,000 procedures. The number varies widely; however, it has been well established that complication rates are higher in facilities where physicians are training than in facilities where only experienced practitioners perform the procedures.


The complications of first- and second-trimester pregnancy termination consist of those that occur at the time of the procedure: inability to dilate the cervix, hemorrhage, uterine perforation and failure to obtain gestational tissue in early gestations; and those that take place in the following days to weeks: retained products of conception and infection.


Inability to dilate the cervix


Difficulty with cervical dilation is most likely to occur among nulliparous women and women who have undergone cesarean section or other surgery affecting the cervix. In these circumstances prostaglandin use leaves few recalcitrant cases. However, direct ultrasound observation of dilator placement may be used to facilitate dilation and avoid creation of a false tract or perforation. The most common prostaglandin used today is misoprostol (Cytotec), an E1 prostaglandin analog that is inexpensive, stable at room temperature and well tolerated. Although not FDA approved as an abortifacient, misoprostol has been safely used for more than a decade. In our experience, in the first trimester 400 μg of buccal misoprostol used at least 90 minutes prior to the procedure leaves the cervix sufficiently softened so that dilation is often no longer necessary.


In second-trimester gestations, osmostic dilators, natural or synthetic, such as Laminaria japonicum, Dilapan or Lamicel may be used prior to prostaglandin use. These materials are compressed tents that slowly expand with the absorption of fluid, dilating the cervix for up to 24 hours prior to the procedure. If more dilation is needed in later terminations, a new set of the osmotic dilators can be placed the morning of the procedure. Misoprostol is often added in later terminations for additional cervical softening and dilation, prior to dilation and evacuation (D&E).


Uterine hemorrhage


Hemorrhage is defined as greater than 500 mL of blood loss. It is an infrequent event during or after pregnancy termination, particularly during a first-trimester procedure (<1%) in which blood loss is routinely less than 15 mL. In second-trimester procedures, specifically those 18 weeks’ gestation and greater, the use of contractile agents such as 20–30 units of oxytocin diluted in a liter of saline or lactated Ringer’s solution started prior or during the procedure, and 0.2 mg ergonovine maleate (Methergine), given intramuscularly or intracervically after completion of the procedure, significantly reduces the risk of substantial blood loss (1–2%). The inclusion of four units of vasopressin in the paracervical anesthesia decreases blood loss by half during both first- and second-trimester procedures.


The most likely cause of minor bleeding is trauma to the external os, usually due to the tenaculum. This diagnosis is made by simple observation and treated with pressure, with or without the application of procoagulants such as silver nitrate or Monsel’s solution. Suture placement is rarely necessary. If the anatomy allows, the instrument holding the cervix can be a curved Allis clamp or ring forceps instead of a tenaculum.


The most common cause of hemorrhage in the second trimester is uterine atony, for which a careful bimanual exam is diagnostic. In this case, vigorous bimanual massage and the above-mentioned uterotonics are extremely helpful first-line therapies. Other treatments include 800–1000 μg of rectal misoprostol or 250 μg of carboprost tromethamine (Hemabate), a 15-methyl F2-α prostaglandin, given intramuscularly at 15-minute intervals for up to eight doses.


If bleeding continues, other causes such as uterine perforation, abnormal placental attachment, i.e. placenta accreta, incomplete evacuation, and cervical laceration must be considered. Uterine perforation just above the internal cervical os may cause hemorrhage into the broad ligament. Diagnosis of broad ligament hematomas can be elusive, as the bleeding is often into the peritoneal cavity instead of into the vagina. The possibility of bowel damage exists as well. If these problems are suspected, definitive diagnosis will necessitate laparoscopy or most commonly exploratory laparotomy.


Cervical laceration at the utero-cervical junction, where the cervical branch of the uterine artery is located, is significantly more likely to occur during second-trimester than first-trimester procedures. This laceration is usually caused by a stretch injury at the time of dilation or in later procedures, removal of sharp calcified fetal parts that have not been adequately crushed prior to removal. Laparoscopy or laparotomy may be required in the presence of ongoing brisk bleeding or signs of hemodynamic instability. These are surgical emergencies and if suspected, expeditious movement is required. Uterine artery embolization can be performed, but only if a team with expertise and experience can be rapidly mobilized. Failure to recognize these emergencies can result in significant morbidity and possibly death. Cervical lacerations are preventable preoperatively with adequate cervical preparation using misoprostol in combination with osmotic dilators, and intraoperatively with sufficient decompression of bony fetal parts prior to removal.


Uterine perforation

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Jun 6, 2016 | Posted by in GYNECOLOGY | Comments Off on Complications of Surgical Abortions

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