Updated: Oct 5, 2009
Prior to the 1960s, female sterilization in the United States was generally performed only for medical indications (when additional pregnancies would be hazardous to the mother). Many centers used a formula (endorsed by the American College of Obstetricians and Gynecologists until 1969) in which age multiplied by parity had to be greater than or equal to 120 before elective sterilization could be considered. The changing cultural climate in the 1960s encouraged women to reduce family size. The popularization of sex steroid hormone contraception (oral contraception) is credited for beginning the sexual revolution and allowing women to use safe, reversible contraception that also provided noncontraceptive benefits.
During the same decade, surgical advances resulted in safe, less invasive female sterilization procedures when childbearing was no longer desired. Most importantly, insurance companies began to cover female sterilization procedures, making the procedure accessible to millions of women in the United States previously unable to afford the surgery.
Currently, approximately 700,000 bilateral tubal sterilizations are performed annually in the United States. Of these, half are performed postpartum and half are ambulatory interval procedures. Eleven million US women aged 15-44 years rely on bilateral tubal occlusion for contraception, and more than 190 million couples worldwide use surgical sterilization as a safe and reliable method of permanent contraception.
Procedures to block the fallopian tube may be divided into those performed at the time of delivery or shortly thereafter, and those performed at another time. The latter are referred to as interval sterilization procedures. Minilaparotomy (Uchida, Pomeroy, or Parkland technique) is the most common procedure in the immediate postpartum period, performed via periumbilical incision following vaginal delivery. The proximity of the uterine fundus in relation to the umbilicus during the immediate postpartum period facilitates this approach. However, there is a much higher incidence of poststerilization remorse associated with procedures performed immediately following delivery.
The laparoscopic approach may be used at any time other than the postpartum period and involves either a single umbilical 10 mm port, or a smaller umbilical camera port and a secondary suprapubic port through which the various devices are introduced.
Although local anesthetic techniques have been described and used for transabdominal approaches, the vast majority of intraperitoneal tubal interruption procedures in the United States are performed using general or spinal anesthesia. And by definition, all require incisions that invade the peritoneal cavity, thereby introducing complications related to general or spinal anesthesia as well as injury to intra-abdominal structures.
Several attempts have been made in the past to achieve transcervical tubal blockage using radiofrequency, chemical scarring with quinacrine, and the injection of liquid silicone. However, these have all failed for safety or efficacy reasons.
In November 2002, the Food and Drug Administration approved the use of Essure microinserts (Conceptus, Inc, Mountain View, Calif) for hysteroscopic sterilization. The devices consist of polyethylene terephthalate (PET) fibers wrapped around a stainless steel core, surrounded by 24 coils of nickel-titanium alloy. After the microinserts are deployed, the PET fibers induce the tubal epithelium to undergo fibrosis, which results in proximal tubal occlusion. This process takes approximately 3 months to form complete occlusion, which is then documented by a hysterosalpingogram.
Tubal sterilization results in mechanically blocking or interrupting the fallopian tubes to prevent sperm from fertilizing the egg.
Tubal sterilization is indicated for women who want a permanent method of contraception and are free of any gynecologic pathology that would otherwise dictate an alternate procedure. Tubal sterilization is also indicated for women in whom a pregnancy could represent a significant clinical and medical risk.
Although the mesonephric (wolffian) ducts degenerate in females, duct remnants may be sites of cyst formation.
Patient ambivalence regarding sterilization is an absolute contraindication. Even though surgically reversing the tubal occlusion at a later date or becoming pregnant through in vitro fertilization is technically feasible, the decision to proceed with sterilization should be considered permanent and irreversible. The cost and disability associated with tubal occlusion is miniscule compared with the expense and time involved in either tubal reanastomosis or assisted reproductive technologies. While the patient should make the request herself, be of sound mind, and not act under external duress; the physician should provide patients who have decided that their families are complete with information regarding the various sterilization options. Many patients may not be aware that a nonincisional, in-office, hysteroscopic method is available. If there is any doubt whatsoever, other long-term but not irreversible methods of contraception, such as the IUD, should be considered when not contraindicated.
Special legal and ethical criteria must be met in cases where the patient undergoing sterilization has a physical, psychological, or intellectual disability.
Any gynecologic malignancy or symptomatic gynecologic pathology (eg, pelvic relaxation, uterine tumors, ovarian tumors) in which a hysterectomy is indicated obviates the need for a tubal occlusion.
In the puerperium, defer sterilization if maternal or infant complications exist. While sterilizations performed in the immediate postpartum are accompanied by a high incidence of regret, even when both mother and baby are healthy, many physicians advocate performing all sterilizations as an interval procedure.
The laparoscopic approach is relatively contraindicated in patients with a diaphragmatic hernia (through the foramen of Morgagni). Limit the Trendelenburg position to 15°, limit intra-abdominal pressure to a maximum of 10 mm Hg, and perform the operation under endotracheal anesthesia.
The laparoscopic approach is also contraindicated in patients with severe cardiopulmonary disease or dysfunction. The pneumoperitoneum may compress the vena cava and azygous system and diminish cardiac return, leading to cardiac decompensation. The diaphragm may be splinted (thus reducing respiratory tidal flow) both by the weight of the intraabdominal
organs, which fall cephalad with the patient in the Trendelenburg position, and by the pneumoperitoneum. Absorption of gas from the pneumoperitoneum may further aggravate the build up of carbon dioxide. The resultant hypercarbia may cause cardiac arrhythmias.
Special consideration must be given to obese patients, who make up an increasingly large percentage of the population. The presence of morbid obesity and/or a history of multiple abdominal surgeries with adhesion formation takes the laparoscopic approach to sterilization out of the realm of elective, low-risk surgery. It would be difficult to justify the selection of a laparoscopic approach in such patients when lower-risk procedures are available.
A publication by the FDA reviewed the incidence of trocar injuries that were reported to the FDA. Between 1997 and 2002, 1300 trocar injuries and 30 deaths were reported, yielding a trocar-related injury rate of 3%. Not counting bowel injury from electrosurgery, wound infection, urinary tract infection, or anesthetic complications, with 300,000 laparoscopic sterilizations performed in the United States each year, that translates to a minimum of 9000 complications from laparoscopic sterilization each year.4
According to the United States Collaborative Review of Sterilization, the odds ratio of complications from general or regional anesthesia is approximately 3 times that of local anesthesia.
The hysteroscopic insertion of microinserts for tubal occlusion may be safely performed in a physician's office under local anesthesia. It does not carry the operative risks incident to laparoscopy such as injury to bowel, bladder, or major vessels caused by trocar insertion or energy sources. The hysteroscopic approach may be safely used in cases of morbid obesity, abdominal scarring, and pelvic adhesions that would otherwise impede the abdominal approach to the fallopian tube. The hysteroscopic microinsert is contraindicated in patients allergic to nickel or contrast media, patients with active PID, patients in whom only 1 microinsert may be inserted, pregnancy, suspected pregnancy, or within 6 weeks of delivery or pregnancy termination.
Surgical approaches for female sterilization include laparoscopy, hysteroscopy, microlaparoscopy, laparotomy (concurrent with cesarean delivery), minilaparotomy, and vaginal approaches. Although minilaparotomy is the most common approach worldwide, laparoscopy is used most commonly for interval procedures in the United States. Hysteroscopic procedures are rapidly gaining popularity. For postpartum procedures, although some studies describe successful use of laparoscopy, the subumbilical minilaparotomy is used most commonly in the United States and worldwide. Vaginal colpotomy approaches are rarely used because they are associated with a higher incidence of infection and can no longer be recommended.
Local anesthesia is used for more than 75% of sterilizations worldwide. Although some US providers use local anesthesia for laparoscopic sterilization, general anesthesia (for interval procedures) and regional anesthesia (for postpartum procedures) are most common.
For the hysteroscopic approach, local anesthesia is the standard approach, and it may be supplemented by oral or IV sedation as needed.
Puerperal tubal sterilization
In comparison with interval sterilization, infraumbilical minilaparotomy following delivery in the early puerperium is convenient, simple, and cost effective. However, if maternal or infant complications exist, sterilization should be delayed.
Bilateral tube ligation (BTL) may be performed after closure of the uterine incision during cesarean delivery or following completion of a vaginal delivery within 72 hours. Postpartum BTL is technically simple because the uterine fundus is at the level of the umbilicus, making the fallopian tubes readily accessible through a small periumbilical abdominal incision.
If the procedure is delayed for several days or if the patient has a significantly involuted uterus (as might occur after delivery of a preterm infant), then delaying to an interval procedure is usually prudent, although puerperal laparoscopic BTL has been reported.
Minilaparotomy
Minilaparotomy is defined as a laparotomy with an incision size smaller than 5 cm. The operation can be performed through a suprapubic incision in the interval after pregnancy and through a subumbilical incision within the first 48 hours after delivery.
A 2- to 5-cm periumbilical semilunar incision is made with the skin tented with Allis clamps. Dissection is carried down to the fascia, which is grasped with hemostats or Allis clamps and opened transversely, exposing the peritoneum, which can then be entered sharply. With uterine manipulation and retraction, the tubes can be visualized and grasped with a Babcock clamp. Often, the oviducts can be palpated at their utero-tubal junction and the uterus may then be rotated to position the isthmus of the tube under the incision anteriorly with the aid of Army-Navy retractors. The fallopian tube is "walked" with Babcock clamps until the fimbriated end is identified. A major cause of failure of sterilization is the inadvertent ligation of the round ligament mistakenly identified as the fallopian tube.
After the BTL, the minilaparotomy incision is closed in layers. Closure of the peritoneum is optional. The fascia is closed with running 2-0 or 0 delayed absorbable suture. Subcutaneous closure is optional, and the skin is closed with 3-0 or 4-0 absorbable suture in a subcuticular manner or with acrylic glue.
Laparoscopy
Advantages include small incisions, full access to the oviducts, rapid recovery, and the ability to inspect the pelvis and upper abdomen.
Disadvantages include the need for general anesthesia, the risks of vessel/viscera injury with needle insufflation/trocar entry, and difficulty associated with laparoscopy in patients who are obese or in the presence of abdominal and/or pelvic adhesions. Entry accounts for 30-50% of all laparoscopic sterilization complications.
The failure rate of the laparoscopic approach according to the US Collaborative Review of Sterilization (CREST) ranges from 7.5 per 1000 procedures for unipolar coagulation to a high of 36.5 per 1000 for the spring clip. The Filshie clip was not included in the CREST study, but its failure rate is reported to be between 1 and 2%.
The patient should always have an examination under anesthesia, and the bladder should be catheterized. A uterine manipulator and the use of the Trendelenburg position enhance exposure.
Microlaparoscopy
Microlaparoscopy involves use of 1.2- to 2-mm microendoscopes with 5- to 7-mm suprapubic ports for bipolar coagulation or mechanical occlusive devices. This surgery is possible because of improved technology in light transmission and fiberoptic bundles.
The theoretical advantages of less pain, less cost, and faster patient recovery have not been assessed through randomized, controlled trials, although several studies have been reported in an office setting. Despite almost 20 years of availability, office microlaparoscopy has not become widely accepted.
Hysteroscopy
Advantages include offering the most cost-effective, minimally invasive approach without the need for abdominal incisions or general anesthesia, thereby avoiding complications associated with trocar injury or thermal burns. Hysteroscopy is regularly performed in an office setting using local anesthesia, thus affording patients a rapid return to normal activity (usually within 24 hours). Compared with laparoscopic techniques, hysteroscopic sterilization studies cite cost savings of >50% in the OR.5,6,7 Prior abdominal surgery and obesity are not contraindications for hysteroscopy, nor are cardiovascular or anatomic contraindications to general anesthesia. Long-term 5-year Essure data from the Phase II and Pivotal Trial continue to demonstrate safety, high patient satisfaction with zero reported pregnancies.8
Essure has been shown to be 99.80% effective in preventing pregnancy after 4 years of follow-up. Essure labeling reports a bilateral placement rate of 94.6%.9 and published papers report placement rates ranging from 96-99%.10,11,12,13,14,15 Since its approval in the commercial setting, the evaluable performance of Essure is still consistent with the age-adjusted effectiveness of 99.85%.8 The hysteroscopic failure rate is the lowest of any surgical approach with 0.5/1000 at 1 year.
Hysteroscopy requires an FDA-mandated hysterosalpingogram to confirm correct placement and to document tubal occlusion. Patients often find this procedure a reassuring confirmation that the tubes are indeed occluded.
Informed consent and preoperative counseling
Inform the patient that a sterilization procedure is intended to be permanent and irreversible and that, as with any form of contraception, a small chance of failure exists. In some languages, sterilization is synonymous with castration. Therefore, the patient must have a very clear grasp of the surgical procedure; diagrams and take-home pamphlets are helpful.
The relative likelihood of an ectopic pregnancy is increased when sterilization failure occurs in all procedures involving occlusion or excision of the isthmic or ampullary segments of the tube, but ectopic pregnancy has not been demonstrated in the hysteroscopic approach. Inform the patient that complications exist, although the incidence of major complications is low. For minilaparotomy and laparoscopic techniques, complications may include injuries to the gastrointestinal and genitourinary tracts, infection, hemorrhage, and complications of anesthesia. For the hysteroscopic approach, the same complications associated with diagnostic hysteroscopy apply — uterine perforation, bleeding, excessive absorption of distention media, and infection.
Alternatives to permanent female sterilization include vasectomy and reversible methods of contraception (eg, injectable and implantable progestins, the levonorgestrel intrauterine system and other commercially available intrauterine devices). Although reversible methods of contraception (eg, injectable and implantable progestins, the levonorgestrel intrauterine system and other commercially available intrauterine devices) are sometimes prescribed in lieu of a permanent solution, these methods are associated with hormonal side effects such as irregular uterine bleeding and are not intended as long-term solutions. For example, Mirena labeling counsels that their product should only be used for up to 5 years for pregnancy prevention.
Screen for risk indicators for regret, including young age, low parity, single parent status, or marital instability. Stress the need to use condoms for protection against sexually transmitted diseases and HIV infection if the patient is at risk of exposure. Document the informed consent process in the patient's medical record. The patient should also receive a copy of the completed consent form to review and retain.
Physicians must be aware of and follow any applicable federal and state requirements regarding informed consent for sterilization procedures, including time intervals between consent and sterilization. If federal funds are used for the procedure, the required US Department of Health and Human Services consent form must be signed 30-180 days prior to surgery. Furthermore, this consent cannot be obtained if the patient is younger than 21 years, in labor, under the influence of drugs or alcohol, mentally incompetent, or having an abortion.
Review the preoperative history and perform a physical examination to determine if any contraindications exist for elective surgery.
Intraoperative details are described for puerperal techniques, laparoscopic approaches, and mechanical techniques.
The follow-up visit for open or laparoscopic approaches is 1-2 weeks postoperatively. Instruct the patient to notify her health care provider if she develops fever (38°C or 100.4°F), increasing or persistent abdominal pain, or bleeding or purulent discharge from the incision.
Patients who have undergone hysteroscopic sterilization must be counseled to use an alternate form of contraception for 3 months at which time a low-pressure hysterosalpingogram must be obtained to confirm placement and bilateral tubal occlusion. The importance of the 3-month hysterosalpingogram needs to be communicated to patients at the time of microinsert placement; subsequent office follow-up may be required to ensure patients comply with confirmation test.
Inform all women who have undergone sterilization about the signs and symptoms of pregnancy (eg, amenorrhea, vaginal bleeding/spotting, abdominal pain) and ectopic pregnancy, and advise these women to seek immediate medical attention if such signs occur.
Mortality
The risk of death from tubal sterilization is 1-2 cases per 100,000 procedures; most of these are complications of general anesthesia. The most common cause of death during laparoscopic BTL appears to be hypoventilation related to anesthesia. Cardiopulmonary arrest and hypoventilation are reported as the leading cause of death in most cases. Sepsis as a cause of
death from laparoscopic sterilization is directly related to bowel perforations or electrical bowel burns. The mortality rate is low when compared with the risk of death from hysterectomy (5-25 cases per 100,000 procedures) and from pregnancy (8 cases per 100,000 live births in the United States and 500 cases per 100,000 live births in developing countries).
No deaths have been reported from the hysteroscopic approach.
Unintended laparotomy
Unintended laparotomy occurs with 1-2% of laparoscopic procedures; most of these conversions are attributable to technical inability to complete the laparoscopic procedure rather than to complications of the procedure.
Bowel injury
Bowel injury can occur during insertion of the insufflation needle or trocar or during electrocoagulation. Small injuries from the needle or trocar with no bleeding or leakage of enteric contents can usually be managed expectantly; otherwise, prompt laparotomy is indicated.
Vascular injury
Vascular injury can occur during insufflation needle or trocar insertion. Injury to a large vessel is a life-threatening emergency. Perform an immediate laparotomy with direct pressure over the injury to control bleeding until repair (usually by a vascular surgeon) can be performed.
Method failure (pregnancy or ectopic pregnancy)
Although sterilization is highly effective and considered the definitive form of pregnancy prevention, it has a failure rate during the first year of 0.1-0.8%. At least one third of these are ectopic pregnancies. Recent findings suggest that pregnancy is somewhat more common than previously estimated, that the risk of pregnancy persists for many years after sterilization, and that the risk varies by method and patient age at sterilization.
In the CREST study, 10,685 women were enrolled from 1978-1986; follow-up continued until 1994. The CREST study reviewed procedures performed at 10 large teaching institutions, and the data may not reflect the experience from the private sector. Whether the findings can be extrapolated to the general population is unclear. In addition, the Filshie clip, which has a
lower incidence of failure than the other laparoscopic techniques, was not included in this study. The 10-year cumulative probability of pregnancy varied from 7.5 cases per 1000 procedures for postpartum partial salpingectomy and unipolar coagulation to 36.5 cases per 1000 procedures for spring clip application. The CREST study identified a 10-year cumulative
failure rate of 18.5 failures per 1000 patients for all methods combined. Pregnancies occurring in the 10th year after sterilization were identified for all methods of laparoscopic occlusion evaluated.
The risk of pregnancy varied by patient age at sterilization and by method, with the highest risk among young women sterilized with bipolar coagulation (54.3 cases per 1000 procedures). Overall, women sterilized at age 34-44 years were half as likely to become pregnant after sterilization compared to women sterilized at age 28-33 years and were approximately one third as likely to become pregnant as women sterilized at age 18-27 years. When pregnancy occurs after BTL, the risk of ectopic pregnancy is high. The CREST study reported a 32% rate of ectopic pregnancy following tubal ligation. Several studies suggest that the risk is highest after bipolar coagulation, with more than 50% of pregnancies being ectopic.
BTL failures can be grouped into the following categories:
Pain
After laparoscopy, patients may experience some degree of chest and shoulder pain due to trapped gas. Mechanical blocking devices are believed to cause ischemic pain, but this has not been established in a randomized, controlled trial. Mild analgesics are usually sufficient to control postprocedure pain.
Hysteroscopic sterilization has been reported to be similar to the pain experienced during menses and is generally limited to the procedure and immediate postprocedure time period.17,18
Infection/hemorrhage
Wound infections and hematoma have been associated with minilaparotomy. Pelvic infections and hemorrhage are associated with vaginal approaches. Although prophylactic antibiotics are recommended for women at risk for subacute bacterial endocarditis who are scheduled to undergo a procedure that may lead to bacteremia, the American Heart Association does
not recommend antibiotic prophylaxis for BTL. Hemorrhage is a rare complication (30-90 cases per 100,000 procedures) that usually occurs following major vessel injury during laparoscopic entry and occasionally occurs following mesosalpingeal vessel injury during the occlusion procedure.
Visceral (bowel, bladder, uterus) injuries
Organ injuries can occur from sharp trauma (eg, insufflation needle, trocar, scalpel), blunt trauma (eg, from adhesiolysis), or electrical-thermal trauma. Injuries can also occur during inadvertent application of the occlusion device to the incorrect structure. If recognized at the time of occurrence, injuries to the bowel and bladder (which are more common in the presence of adhesions) are relatively easy to manage and will not result in long-term adverse sequelae. Injuries to the uterus, most often caused by uterine manipulators, do not usually lead to adverse sequelae unless bowel or bladder has been perforated simultaneously.
Patient regret
Sterilization is intended to be permanent, but patient regret is not rare. Poststerilization regret is a complex condition often caused by unpredictable life events. Risk factors for regret that may be useful in presterilization counseling include young age, low parity, and single parent status or being in an unstable relationship. As many as 6% of women who are sterilized report
regret or request information about tubal reversal within 5 years of the procedure. Follow-up interviews 14 years postprocedure demonstrate that regrets were expressed by 20.3% of women aged 30 years or younger at the time of BTL and by 5.9% of women older than 30 years at time of procedure.
The proportion of women who actually undergo microsurgical tubal reanastomosis is only 0.2% in the first 5 years after BTL. The most important factor in determining the success of reversal by tubal anastomosis is the length of healthy tube remaining after sterilization. Isthmic-to-isthmic anastomoses are most likely to be successful.
Noncontraceptive benefits are as follows:
Ovarian cancer
Several studies report a protective effect of sterilization against ovarian cancer, with a relative risk ranging from 0.2-0.8. Protection is hypothesized to result from reduced exposure of the ovaries to potential environmental carcinogens and infectious sources of malignant transformation (eg, oncogenic viruses).
Pelvic inflammatory disease
Although BTL does not protect against the acquisition of sexually transmitted disease, sterilization has been demonstrated to reduce the spread of organisms from the lower genital tract to the peritoneal cavity and thus protect against PID. Studies have reported that PID is less common in women who are sterilized compared with women who are not sterilized; however, protection is not absolute because uncommon reports exist of PID in sterilized women within 4-6 weeks or several years following surgery.
In cases of infection occurring within weeks of surgery, manipulation of the cervix, uterus, or oviducts is postulated to exacerbate a chronic infection or facilitate bacterial ascent from the lower genital tract at the time of surgery (eg, chlamydial or gonococcal cervicitis). PID occurring years after BTL results from bacteria ascending through a uteroperitoneal fistula or spontaneously recanalized tube. In these situations, if the patient requires surgery for diagnosis or treatment, relegating or excising the oviducts to help prevent future episodes of infection and ectopic pregnancy is prudent. Case reports have also demonstrated abscesses in the stump of the proximal fallopian tube.
Future methods
Researchers continue to explore the possibility of using various substances that can be introduced through the cervix to occlude the tubal lumen through sclerosis or mechanical occlusion.
Quinacrine (historically used as an antimalarial drug) used for sterilization is instilled into the oviducts via transcervical application through a modified copper T intrauterine device. Although not approved for sterilization purposes in any country, an estimated 100,000 women have undergone this method of sterilization. The mechanism of action is tubal occlusion caused by inflammation and fibrosis of the intramural portion of the tube. Long-term failure rates, complications, optimal doses, and the need for adjuvants (eg, nonsteroidal anti-inflammatory drugs) are not clear because of nonsystematic investigation of the method and poor follow-up of women who have received it. Toxicologic studies and follow-up data are needed before the initiation of any human trials in the United States.
Post–tubal ligation syndrome
Proposed in 1951, this syndrome is a controversial constellation of symptoms, including pelvic discomfort, ovarian cystic changes, and menorrhagia, which are suggested to occur as a result of disruption of the uteroovarian blood supply, with resultant disturbances of ovulatory function after BTL. Often, these patients have a history of these problems before BTL or have been taking birth control pills, which masked their symptoms.
After extensive study, BTL apparently causes few, if any, menstrual abnormalities within several years after sterilization, regardless of the method of tubal occlusion used. Data from the CREST study indicate that women who are tubally sterilized are no more likely than women who have not undergone the procedure to report intermenstrual bleeding or changes in
menstrual cycle length. However, women who are sterilized are more likely to report a reduced number of days of bleeding, less overall bleeding and menstrual pain, and increased cycle irregularity. BTL also seems to help reduce blood flow in women who reported very heavy menstrual bleeding at baseline.
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tubal sterilization, bilateral tubal ligation, BTL, bilateral tubal occlusion, female sterilization, elective sterilization, bilateral tubal sterilization, contraception, surgical sterilization, birth control, hysteroscopic sterilization, Falope ring, Filshie clip, hysteroscopic micro-insert, microinsert, micro insert, periumbilical minilaparotomy, tube tying
Robert K Zurawin, MD, Associate Professor, Director of Baylor College of Medicine Program for Minimally Invasive Gynecology, Director of Fellowship Program, Minimally Invasive Surgery, Department of Obstetrics and Gynecology, Baylor College of Medicine
Robert K Zurawin, MD is a member of the following medical societies: American Association of Gynecologic Laparoscopists, American College of Obstetricians and Gynecologists, American Society for Reproductive Medicine, Association of Professors of Gynecology and Obstetrics, Central Association of Obstetricians and Gynecologists, Harris County Medical Society, North American Society for Pediatric and Adolescent Gynecology, and Texas Medical Association
Disclosure: Johnson and Johnson Honoraria Speaking and teaching; Conceptus Honoraria Speaking and teaching; Biosphere Medical Honoraria Speaking and teaching; Eli Lilly Honoraria Speaking and teaching
Avi J Sklar, MD, FRCSC, FACOG, FACS, Co-Chief, Division of Gynecology, Department of Obstetrics and Gynecology, Santa Clara Valley Medical Center
Avi J Sklar, MD, FRCSC, FACOG, FACS is a member of the following medical societies: American College of Obstetricians and Gynecologists, American College of Surgeons, American Society for Colposcopy and Cervical Pathology, Phi Beta Kappa, and Royal College of Physicians and Surgeons of Canada
Disclosure: Nothing to disclose.
Anthony Charles Sciscione, DO, Director, Division of Maternal-Fetal Medicine, Professor, Department of Obstetrics and Gynecology, Drexel University College of Medicine
Anthony Charles Sciscione, DO is a member of the following medical societies: American College of Obstetricians and Gynecologists and American Medical Association
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
Richard S Legro, MD, Professor, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology, Pennsylvania State University College of Medicine; Consulting Staff, Milton S Hershey Medical Center
Richard S Legro, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Society for Reproductive Medicine, Endocrine Society, Phi Beta Kappa, and Society of Reproductive Surgeons
Disclosure: Nothing to disclose.
Frederick B Gaupp, MD, Consulting Staff, Department of Family Practice, Hancock Medical Center
Frederick B Gaupp, MD is a member of the following medical societies: American Academy of Family Physicians
Disclosure: Nothing to disclose.
Michel E Rivlin, MD, Professor, Coordinator of Quality Assurance/Quality Improvement, Department of Obstetrics and Gynecology, University of Mississippi School of Medicine
Michel E Rivlin, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Medical Association, Mississippi State Medical Association, and Royal College of Surgeons of Edinburgh
Disclosure: Nothing to disclose.
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