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Surg Endosc (2008) 22:849861 DOI 10.

1007/s00464-008-9758-6

GUIDELINES

Guidelines for diagnosis, treatment, and use of laparoscopy for surgical problems during pregnancy
This statement was reviewed and approved by the Board of Governors of the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES), September 2007. It was prepared by the SAGES Guidelines Committee.
Prepared by the Guidelines Committee of the Society of American Gastrointestinal and Endoscopic Surgeons

Received: 26 December 2007 / Accepted: 8 January 2008 / Published online: 21 February 2008 Springer Science+Business Media, LLC 2008

Preamble Early concerns about the performance of laparoscopic surgery performed on pregnant patients centered on the potential risk to the fetus due to trocar insertion, CO2 insufation, and the technical ability to obtain proper operative exposure with a gravid uterus. Additionally, risks to the mother that were thought to be important included altered physiology of pneumoperitoneum and decreased venous return to the heart. Evidence is accumulating to suggest that clinical outcomes are equivalent to open surgical techniques, while conferring all the advantages of the laparoscopic approach. This document provides specic recommendations and guidelines to assist physicians in the diagnostic workup and treatment of surgical problems in pregnant patients focusing on the use of laparoscopy. Surgical interventions during pregnancy should minimize fetal risk without compromising the safety of the mother.

applicable to all physicians who address the clinical problem(s) without regard to specialty training or interests, and are intended to indicate the preferable, but not necessarily the only, acceptable approaches. Guidelines are intended to be exible. Given the wide range of specics in any health care problem, the surgeon must always choose the course best suited to the individual patient and the variables in existence at the moment of decision. Guidelines are developed under the auspices of the Society of American Gastrointestinal Endoscopic Surgeons and its various committees, and approved by the Board of Governors. Each clinical practice guideline has been systematically researched, reviewed, and revised by the guidelines committee, and reviewed by an appropriate multidisciplinary team. The recommendations are therefore considered valid at the time of production based on the data available. Each guideline is scheduled for periodic review to allow incorporation of pertinent new developments in medical research knowledge, and practice.

Disclaimer Guidelines for clinical practice are intended to indicate preferable approaches to medical problems as established by experts in the eld. These recommendations will be based on existing data or a consensus of expert opinion when little or no data are available. Guidelines are
This is a revision of SAGES Publication #0023, originally printed 10/00. H. Yumi (&) Society of American Gastrointestinal and Endoscopic Surgeons 11300 W, Olympic Blvd. Suite 600, Los Angeles, CA 90064, USA e-mail: SAGESweb@sages.org; yumi@sages.org

Background Approximately 1 in 500 to 1 in 635 women will require nonobstetrical abdominal surgery during their pregnancy [1, 2]. The most common nonobstetrical surgical emergencies complicating pregnancy are acute appendicitis, cholecystitis, and intestinal obstruction [1]. Other conditions that may require surgery during pregnancy include ovarian cysts, masses or torsion, symptomatic cholelithiasis, adrenal tumors, splenic disorders, symptomatic hernias, complications of inammatory bowel diseases, and abdominal pain of unknown etiology. All of these diseases are routinely treated using laparoscopic techniques in the nonpregnant patient with good outcomes.

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During its infancy, some argued that laparoscopy was contraindicated during pregnancy. Many now utilize laparoscopy as an alternative to open surgery in order to provide the pregnant patient with the same benets of a minimally invasive approach that nonpregnant patients have realized. Many of the issues related to the minimally invasive approach for surgical treatment of diseases during pregnancy have been claried with the accumulation of data from its increased use and acceptance during pregnancy [3]. Denitions The denition document has been prepared and published by the SAGES Guidelines Committee.

causes of abdominal pain including adnexal mass, torsion, placental abruption, placenta previa, uterine rupture, and fetal demise. Ultrasound is also useful as a rst-line diagnostic study for many nongynecologic causes of abdominal pain, potentially allowing the practitioner to avoid the need for ionizing radiation exposure [511]. Risk of ionizing radiation Guideline 2: Expeditious and accurate diagnosis should take precedence over concerns for ionizing radiation. Radiation dosage should be limited to 510 rads in the rst 25 weeks of pregnancy (Level III, Grade B). Signicant radiation exposure may lead to chromosomal mutations, neurological abnormalities, mental retardation, and increase the risk of childhood leukemia. Radiation dosage is the most important risk factor but fetal age at exposure is also important [7, 8, 12]. Radiological exposure is measured using units of either rad or centiGrey (1 rad = 1 cGy). Fetal mortality is greatest when exposure occurs within the rst week of conception prior to oocyte implantation. It has been recommended that the cumulative radiation dose from the rst week of conception through week 25 be less than 510 rads [13]. The most sensitive time period for central nervous system (CNS) teratogenesis is between 10 and 17 weeks gestation and nonurgent X-rays should be avoided during this time. In later pregnancy the concern shifts from teratogenesis to increasing the risk of childhood hematologic cancer. The background incidence of childhood cancer and leukemia is approximately 0.2 0.3%. Radiation may increase that incidence by 0.06% per 1 rad delivered to the fetus [13]. Exposure of the fetus to 0.5 rad increases the risk of spontaneous abortion, major malformations, mental retardation, and childhood malignancy to one additional case in 6,000 above baseline risk. It has been suggested that fetal risk is negligible at 5 rads or less and that the risk of malformation is signicantly increased at doses above 15 rads. The accepted cumulative dose of ionizing radiation during pregnancy is 510 rads with no single diagnostic study exceeding 5 rads [8, 1217]. Computed tomography (CT) Guideline 3: Contemporary multidetector CT protocols deliver a radiation dose to the fetus below detrimental levels and may be considered as an appropriate test during pregnancy depending on the clinical situation (Level III, Grade B). Computed tomography (CT) has a well-established role as a diagnostic modality in the nonpregnant patient. Many of the same nonobstetric indications for its use can also be found in a woman during pregnancy [18]. Employment of

Diagnosis and Workup Abdominal pain in the gravid patient presents a dilemma in which the clinician must weigh the risks and benets of potential diagnostic modalities and therapy not only to the mother but also to the fetus. The clinical issues and pathological conditions differ between the trimesters of pregnancy. These guidelines assume intrauterine pregnancy has been conrmed. An underlying principle to the workup of abdominal pain was stated by Sir Zachary Cope in 1921, Earlier diagnosis means better prognosis. [4]. Although fetal safety during diagnostic imaging is an important goal for clinicians and patients, the benets to the mother outweigh the risk to the fetus, bearing in mind that the risk of fetal morbidity and mortality also increases when the mother is faced with an acute surgical disease. Imaging techniques A riskbenet discussion with the patient should be undertaken prior to initiating any diagnostic study.

Ultrasound Guideline 1: Ultrasonographic imaging during pregnancy is safe and useful in identifying the etiology of acute abdominal pain in the pregnant patient (Level II, Grade A). Abdominal pain in the pregnant patient can be separated into gynecologic and nongynecologic causes. When radiographic studies are needed, ultrasound is widely considered safe for the mother and fetus with relatively high sensitivity and specicity for many intra-abdominal processes. No maternal or fetal adverse effects have been reported. It is the radiographic test of choice for most gynecologic

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the CT scan should be weighed against the cumulative radiation exposure to the fetus. As a single test, radiation exposure to the fetus is highest when a full scan of the abdomen and pelvis is obtained, reaching exposure levels up to 24 rads for a single study [7, 19, 20], which falls below the maximum recommended dose of 5 rads for a single study. Advancements in CT technology and protocols have led to decreased radiation doses. These levels vary by institution and the practitioner should be aware of the potential radiation exposure. Magnetic resonance (MR) imaging Guideline 4: MR Imaging can be performed at any stage of pregnancy without the use of intravenous gadolinium (Level III, Grade B). MRI provides excellent soft-tissue multiplanar imaging without ionizing radiation. It is generally considered safe in pregnancy as no ionizing radiation is employed, although further research is needed. It should be used after a clinical riskbenet analysis is discussed between the clinician and the patient [2125]. Intravenous gadolinium agents do cross the placenta and any effects are not fully understood; therefore their use during pregnancy is controversial [22]. Nuclear medicine Guideline 5: Nuclear Medicine administration of radio nucleotides can generally be accomplished at fetal radiation levels of exposure that are well below any known detrimental levels (Level III, Grade C). Radiopharmaceuticals, including technetium99 m, can generally be administered at doses that provide whole fetal exposure of less than 0.5 rad [26], well within the known safe range of fetal exposure. Consultation with a nuclear medicine radiologist or technologist should be considered prior to performing the study. The study should be commensurate with the most expeditious and accurate method of securing the suspected diagnosis.

radiation dose of up to 20 rads/minute, but varies depending on the X-ray equipment utilized, patient positioning, and patient size. Radiation exposure is cumulative, suggesting that a selective approach to exposure of the pregnant patient to uoroscopy is prudent. During cholangiography, the fetus should be shielded as able. Placing a lead apron inside an impermeable sterile drape during surgery is helpful in accomplishing this goal. No adverse effects have been reported from cholangiography specically. Magnetic resonance cholangiopancreatography (MRCP) is an alternative approach, but is only diagnostic and accuracy will vary amongst institutions. These facts should be considered when selecting this approach. Endoscopic retrograde cholangiopancreatography (ERCP) also has risks beyond the radiation exposure such as bleeding and pancreatitis. In nonpregnant patients, the risk of bleeding is 1.3% and the risk of pancreatitis is 3.5% [27]. These additional risks warrant the same careful risk benet analysis and discussion with the patient as other operative and procedural interventions [7, 16, 28, 29]. Alternatives to uoroscopy include intraoperative ultrasound and choledochoscopy. These are both acceptable methods provided the surgeon has the appropriate equipment and skills to expeditiously and accurately perform the examinations.

Surgical techniques Guideline 7: Diagnostic laparoscopy is safe and effective when used selectively in the workup and treatment of acute abdominal processes in pregnancy (Level II, Grade B). Diagnostic laparoscopy provides direct visualization of intra-abdominal organs. While not enough data are available to recommend this as a primary diagnostic approach in the pregnant patient, it is certainly a reasonable alternative. The benets of operative exploration are avoidance of ionizing radiation, rapidity, and diagnostic accuracy, as well as the ability to treat a surgical problem at the time of diagnosis. Additionally, it has been shown that laparoscopy can be performed safely during any trimester of pregnancy with minimal morbidity to the fetus and mother [3042].

Cholangiography Guideline 6: Intraoperative and endoscopic cholangiography exposes the mother and fetus to minimal radiation and may be used selectively during pregnancy. The lower abdomen should be shielded when performing cholangiography during pregnancy to decrease the radiation exposure to the fetus (Level III, Grade B). Radiation exposure during cholangiography is estimated to be less than 0.5 rads. Fluoroscopy generally delivers a

Patient Selection Preoperative decision making Guideline 8: Laparoscopic treatment of acute abdominal processes has the same indications in pregnant and nonpregnant patients (Level II, Grade B).

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Once the decision to operate has been made, the surgical approach (laparotomy versus laparoscopy) should be determined based on the skills of the surgeon as well as the availability of the appropriate staff and equipment. Appropriate discussion with the patient regarding the risks and benets of surgical intervention should be undertaken. Benets of laparoscopy during pregnancy appear similar to those benets in nonpregnant patients including less postoperative pain, less postoperative ileus, decreased length of hospital stays, and faster return to work [31, 36, 4346].

postoperative narcotic requirements [36, 5759], lower risk of wound complications [57, 60, 61], diminished postoperative maternal hypoventilation [57, 58], shorter hospital stays, and decreased risks of thromboembolic events due to early mobilization. Laparoscopy reduces the risk of uterine irritability by decreasing the need for uterine manipulation because of improved visualization [62]. Decreased uterine irritability results in lower rates of spontaneous abortion and preterm delivery [63].

Patient positioning Laparoscopy and trimester of oregnancy Guideline 9: Laparoscopy can be safely performed during any trimester of pregnancy (Level II, Grade B). Operative intervention may be performed in any trimester if warranted by the patients condition. Historical recommendations, which were based on experiences with open surgical procedures during pregnancy, were to delay surgery until the second trimester. These recommendations were thought to minimize the spontaneous abortion rate of surgical intervention during the rst trimester, which has been reported to be as high as 12%, and to avoid preterm labor (up to 40%) when surgery occurs during the third trimester [47]. This experience has not been reproduced in more recent literature reporting on laparoscopic cases. Several recent studies have shown that pregnant patients may undergo laparoscopic surgery safely during any trimester without any appreciated increased risk to the mother or fetus [30, 31, 46, 4851]. It has been suggested that delaying surgical intervention in patients with symptomatic gallstone disease during pregnancy may lead to further complications of gallstone disease such as acute cholecystitis and gallstone pancreatitis [48, 5254] which can lead to higher spontaneous abortion rates and preterm labor. It has been suggested that the gestational age limit for successful completion of laparoscopic surgery during pregnancy is 2628 weeks [35]. This has been refuted by several studies in which laparoscopic cholecystectomy and appendectomy have been successfully performed late in the third trimester [49, 51, 55, 56]. Although laparoscopy can be performed safely in pregnancy with good fetal and maternal outcomes, the long-term effects to the children have not been well studied. One recent study evaluated 11 children from 18 years and found no growth or developmental delay [42]. Guideline 10: Gravid patients should be placed in the left lateral recumbent position to minimize compression of the vena cava and the aorta (Level II, Grade B). When the pregnant patient is placed in a supine position, the gravid uterus places pressure on the inferior vena cava, resulting in decreased venous return to the heart. This decrease in venous return results in maternal hypotension, reduction in cardiac output by 10% to 30%, and decreased placental perfusion during surgery [6466]. Placing the patient in a left lateral recumbent position will shift the uterus off the vena cava, improving venous return and cardiac output [64, 65].

Initial port placement Guideline 11: Initial access can be safely accomplished with open (Hassan), Verres needle or optical trocar technique if the location is adjusted according to fundal height, previous incisions, and experience of the surgeon (Level III, Grade B). There has been much debate regarding abdominal access in the pregnant patient with preferences toward either a Hassan technique or Verres needle. The concern for use of the Verres needle technique has largely been based on concerns for higher likelihood of injury to the uterus or other intra-abdominal organs as fundal height increases [67, 68]. Because the intra-abdominal domain is altered by the increasing fundal height, adaptation of the initial access site from the umbilicus to subcostal regions as the uterus enlarges in the second and third trimester has been recommended [49, 51, 55, 62]. If the site of initial abdominal access is adjusted according to fundal height and the abdominal wall is elevated during insertion, both the Hassan technique and Verres needle can be safely and effectively utilized [49, 51, 69]. It has also been recommended that placement of trocars is adjusted according to fundal height and that they are inserted under direct visualization [70, 71]. Ultrasoundguided trocar placement has been described in the literature as an additional method to visualize trocar placement [72].

Treatment There are many advantages of laparoscopy in the pregnant patient including decreased fetal depression due to lessened

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Insufation pressure Guideline 12: CO2 insufation of 1015 mmHg can be safely used for laparoscopy in the pregnant patient. Intra-abdominal pressure should be sufcient to allow for adequate visualization (Level III, Grade C). The potential effects of CO2 insufation on the pregnant patient and her fetus have led to apprehension over its use. The pulmonary effects of pneumoperitoneum in the pregnant patient and the potential risk for acidosis to the fetus have caused concern and have led some investigators to develop alternative approaches of gasless laparoscopy, but these have not been widely adopted [7380]. The pregnant patients diaphragm is upwardly displaced by the growing fetus, which results in decreased residual lung volume and functional residual capacity, making her more susceptible to arterial oxygen desaturation [81]. Upward displacement of the diaphragm by pneumoperitoneum is more worrisome in a pregnant patient with existing restrictive pulmonary physiology. Some have recommended that intra-abdominal insufation pressures be maintained at less than 12 mmHg to avoid worsening pulmonary physiology in this population [71, 82]. Others have argued that insufation less than 12 mmHg may not provide adequate visualization of the intra-abdominal cavity [49, 51]. Pressures of 15 mmHg have been implemented during laparoscopy in pregnant patients without increasing adverse outcomes to the patient or her fetus [49, 51]. Because CO2 exchange occurs with intraperitoneal insufation, there has been concern for effects to the fetus, specically the effects of acidosis. Some animal studies have conrmed fetal acidosis with associated tachycardia, hypertension, and hypercapnia during CO2 pneumoperitoneum [8385]. Other animal studies have demonstrated no fetal acidosis [86]. Regardless, no long-term adverse effects have been identied [8386]. Of more interest, there is no evidence to support long-term detrimental effects resulting from CO2 pneumoperitoneum in humans [35].

blood gas monitoring of arterial carbon dioxide (PaCO2) versus end-tidal carbon dioxide (ETCO2) monitoring, but the less invasive capnography has been demonstrated to reect maternal acid/base status adequately in humans [90]. Several large studies have documented the safety and efcacy of EtCO2 measurements in pregnant women [35, 49, 51], making routine blood gas monitoring unnecessary.

Venous thromboembolic (VTE) prophylaxis Guideline 14: Intraoperative and postoperative pneumatic compression devices and early postoperative ambulation are recommended prophylaxis for deep venous thrombosis in the gravid patient (Level III, Grade C). Pregnancy is a hypercoagulable state with a 0.10.2% incidence of deep venous thrombosis [91]. CO2 pneumoperitoneum may increase the risk of deep venous thrombosis by increasing venous stasis. Even insufation of 12 mmHg causes a statistically signicant decrease in blood ow that cannot be completely reversed with intermittent pneumatic compression devices or intermittent electric calf stimulators [92]. There is unfortunately a paucity of research on prophylaxis for deep venous thrombosis in the pregnant patient. Because of the increased risk of thrombosis, prophylaxis with pneumatic compression devices both intraoperatively and postoperatively and early postoperative ambulation are recommended as they are in the nonpregnant patient. There is no data regarding use of unfractionated or low-molecularweight heparin for prophylaxis in pregnant patients undergoing laparoscopy, though its use has been suggested in patients undergoing extended major surgery [93]. In patients that require anticoagulation during pregnancy, heparin has proven safe with monitoring and is the agent of choice [94].

Gallbladder disease Guideline 15: Laparoscopic cholecystectomy is the treatment of choice in the pregnant patient with gallbladder disease regardless of trimester (Level II, Grade B). Management of symptomatic cholelithiasis in pregnancy has been controversial, with some recommending initial nonoperative management [52, 9597]. Those in favor of early surgical management are supported by the recurrence of symptomatic gallstones during pregnancy in 92% of patients managed nonoperatively who present in the rst trimester, 64% presenting in the second, and 44% in the third [98]. More important than recurrence, this delay in surgical management results in signicant morbidity including increased hospitalizations, spontaneous abortions,

Intraoperative CO2 monitoring Guideline 13: Intraoperative CO2 monitoring by capnography should be used during laparoscopy in the pregnant patient (Level III, Grade C). Fetal acidosis and associated fetal instability in CO2 pneumoperitoneum have been documented in animal studies, though no long-term effects from these changes have been identied [8385, 87]. Fetal acidosis with insufation has not been documented in the human fetus, but concerns over potential detrimental effects of acidosis have led to the recommendation of maternal CO2 monitoring [88, 89]. Initially, there was debate over maternal

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preterm labor, and preterm delivery compared to those undergoing cholecystectomy [39, 40, 52, 8891]. In addition, nonoperative management boasts a reported 57% symptom recurrence during pregnancy in patients with biliary colic and a 23% complication rate of acute cholecystitis and gallstone pancreatitis [48]. Gallstone pancreatitis results in fetal loss in 1060% of pregnant patients [99, 100]. The signicant morbidity and mortality associated with gallbladder disease in the gravid patient argue in favor of surgical management. When compared to open cholecystectomy, the laparoscopic approach has equivalent outcomes and the well established added benets of laparoscopy [50]. Improved outcomes with decreased risk of spontaneous abortion and preterm labor have been reported in laparoscopic cholecystectomy when compared to laparotomy [101].

Choledocholithiasis Guideline 16: Choledocholithiasis during pregnancy may be managed with preoperative endoscopic retrograde cholangiopancreatography (ERCP) with sphincterotomy followed by laparoscopic cholecystectomy, intraoperative laparoscopic transcystic or choledochotomy common bile duct exploration, or postoperative ERCP depending on local resources and clinical scenario (Level III, Grade C). Complications associated with choledocholithiasis are relatively uncommon during pregnancy [102, 103]. However, these complications can result in signicant morbidity and mortality making appropriate management of these patients important. Unfortunately, there have been no trials comparing common bile duct exploration at the time of laparoscopic cholecystectomy to endoscopic retrograde cholangiopancreatography followed by cholecystectomy. Good outcomes have been described with intraoperative common bile duct exploration, but few cases have been reported [104]. Multiple studies have demonstrated safe and effective management of common bile duct stones with endoscopic retrograde cholangiopancreatography with sphincterotomy and subsequent laparoscopic cholecystectomy [105110].

complicated by the anatomic changes and leukocytosis associated with pregnancy [116119]. A recent article, however, has shown that the majority ([ 83%) of gravid patients with acute appendicitis present with classic right lower quadrant pain [120]. Negative appendectomy rates in the gravid patient have been reported to be as high as 22 55% [32, 69]. These high negative appendectomy rates may be due to the surgeons propensity to prevent perforation and avoid unnecessary morbidity and mortality. When the diagnosis of appendicitis by ultrasound is equivocal, promptly proceeding to diagnostic laparoscopy or CT scan may allow for early identication and intervention in appendicitis, decreasing the rate of perforation. Twenty ve percent of all pregnant women who have acute appendicits will develop perforated appendicitis [121, 122]. A 66% perforation incidence has been reported when surgery is delayed by more than 24 h compared to 0% incidence when surgical management is initiated prior to 24 h of presentation [123]. Of note, perforation of the appendix occurs twice as often in the third trimester (69%) compared to the rst and second trimesters [124].

Solid organ resection Guideline 18: Laparoscopic adrenalectomy, nephrectomy and splenectomy are safe procedures in pregnant patients when indicated and standard precautions are taken (Level III, Grade C). After successful laparoscopic management of appendicitis and gallbladder disease in pregnancy, surgeons began exploring laparoscopy in the management of other surgical diseases that arise in pregnancy. Laparoscopic adrenalectomy during pregnancy has proven effective in the management of primary hyperaldosteronism [125], Cushings syndrome [126128], and pheochromocytoma [129134]. Laparoscopic splenectomy has also become an increasingly accepted surgical approach in pregnancy [135]. Gravid patients with antiphospholipid syndrome [136], hereditary spherocytosis [137], and autoimmune thrombocytopenia purpura [135, 138, 139] have undergone laparoscopic splenectomy with excellent outcomes for mother and fetus. More recently, two cases of laparoscopic nephrectomy have been reported in the rst and second trimester without any associated complications and both infants were born healthy at term [140, 141].

Laparoscopic appendectomy Guideline 17: Laparoscopic appendectomy may be performed safely in pregnant patients with suspicion of appendicitis (Level II, Grade B). Laparoscopic appendectomy has become increasingly utilized in the gravid patient since its introduction and is considered by many to be the standard of care [49, 51, 111115]. Diagnosis of appendicitis is thought to be

Adnexal masses Guideline 19: Laparoscopy is safe and effective treatment in gravid patients with symptomatic adnexal cystic masses. Observation is acceptable for all other

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adnexal cystic lesions provided ultrasound is nonworrisome for malignancy and tumor markers are normal. Initial observation is warranted for most adnexal cystic lesions \6 cm in size (Level III, Grade C). The incidence of adnexal masses during pregnancy is 2% [142]. Most of these adnexal masses discovered during the rst trimester are functional cysts that resolve spontaneously by the second trimester [70]. Expectant management has been recommended for B6 cm adnexal masses in the pregnant patient based on an 82% [143] to 94% [144] rate of spontaneous resolution. Persistent masses are most commonly functional cysts or mature cystic teratomas with the incidence of malignancy reported at 26% [145]. Historically, the concern over malignant potential and risks associated with emergency surgery have led to elective removal of masses that persist at 16 weeks and are [6 cm in diameter [144146]. However, recent literature supports the safety of close observation in these patients when ultrasound ndings are not concerning for malignancy, tumor markers are normal (CA125, Lactate dehydrogenase (LDH)) and the patient is asymptomatic [147150]. In the event that surgery is indicated, various case reports support the use of laparoscopy in the management of adnexal masses [151159] in every trimester [160163]. Perhaps more informatively, a retrospective review of 88 pregnant women demonstrated equivalent maternal and fetal outcomes in adnexal masses managed laparoscopically and by laparotomy [62].

Perioperative Care Fetal heart monitoring Guideline 21: Fetal heart monitoring should occur preand postoperatively in the setting of urgent abdominal surgery during pregnancy (Level III, Grade B). While intraoperative fetal heart rate monitoring was once thought to be the most accurate method to detect fetal distress during laparoscopy, no intraoperative fetal heart rate abnormalities have been reported in the literature [48, 101]. This has led some to recommend preoperative and postoperative monitoring of the fetal heart rate with no increased fetal morbidity having been reported [49, 51].

Obstetrical consultation Guideline 22: Obstetric consultation can be obtained pre- and/or postoperatively based on the acuteness of the patients disease, gestational age, and availability of the consultant (Level III, Grade C). Maternal and fetal monitoring should be part of any pregnant patients care and continue throughout their hospitalization, but the timing of a formal obstetric consultation will vary based on availability and the acuteness of the patients condition. Delaying the treatment of an acute abdominal process to obtain such a consultation should be avoided as treatment delay may increase the risk of morbidity and mortality to the mother and fetus [174].

Adnexal torsion Guideline 20: Laparoscopy is recommended for both diagnosis and treatment of adnexal torsion unless clinical severity warrants laparotomy (Level III, Grade C). Of adnexal masses 1015% undergo torsion [164]. Laparoscopy is the preferred method of both diagnosis and treatment in the gravid patient with adnexal torsion [165]. Multiple case reports have conrmed safety and efcacy of laparoscopy for adnexal torsion in pregnant patients [166 170]. If diagnosed before tissue necrosis, adnexal torsion may be managed by simple laparoscopic adnexal detorsion [171]. However, with late diagnosis of torsion adnexal infarction may ensue, which left untreated can result in peritonitis, spontaneous abortion, preterm delivery and death [146, 172]. The gangrenous adnexa should be completely resected [173] and progesterone therapy initiated after removal of the corpus luteum if at less than 12 weeks gestation [171]. Laparotomy may be necessary as dictated by the patients clinical severity and intraoperative ndings [122].

Tocolytics Guideline 23: Tocolytics should not be used prophylactically, but should be considered perioperatively when signs of preterm labor are present in coordination with obstetric consultation (Level I, Grade A). Threatened preterm labor can be successfully managed with tocolytic therapy. The specic agent and indications for the use of tocolytics should be individualized. An obstetric consultation may be necessary as controversy exists over which of several agents is the preferred [175178]. No literature supports the use of prophylactic tocolytics.

Summary of Recommendations More information has accumulated recently as laparoscopy has become more common during pregnancy. However, most of the data is found in case series and retrospective reviews, which limits the ability to provide absolute guidelines. Further controlled clinical studies are needed to

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clarify these guidelines, and revision may be necessary as new data appear. The current recommendations for laparoscopy during surgery are:

radiation and may be used selectively during pregnancy. The lower abdomen should be shielded when performing cholangiography during pregnancy to decrease the radiation exposure to the fetus (Level III, Grade B).

Diagnosis and Workup Surgical Techniques Imaging Techniques Ultrasound Guideline 1: Ultrasonographic imaging during pregnancy is safe and useful in identifying the etiology of acute abdominal pain in the pregnant patient (Level II, Grade A). Guideline 7: Diagnostic laparoscopy is safe and effective when used selectively in the workup and treatment of acute abdominal processes in pregnancy (Level II, Grade B).

Patient Selection Preoperative Decision Making

Risk of Ionizing Radiation Guideline 2: Expeditious and accurate diagnosis should take precedence over concerns for ionizing radiation. Radiation dosage should be limited to 510 rads in the rst 25 weeks of pregnancy (Level III, Grade B). Guideline 8: Laparoscopic treatment of acute abdominal processes has the same indications in pregnant and nonpregnant patients (Level II, Grade B).

Laparoscopy and Trimester of Pregnancy Computed Tomography Guideline 3: Contemporary multidetector CT protocols deliver a radiation dose to the fetus below detrimental levels and may be considered as an appropriate test during pregnancy depending on the clinical situation (Level III, Grade B). Guideline 9: Laparoscopy can be safely performed during any trimester of pregnancy (Level II, Grade B).

Treatment Patient Positioning Guideline 10: Gravid patients should be placed in the left lateral recumbent position to minimize compression of the vena cava and the aorta (Level II, Grade B).

Magnetic Resonance Imaging Guideline 4: MR Imaging can be performed at any stage of pregnancy without intravenous gadolinium (Level III, Grade B).

Initial Port Placement Guideline 11: Initial access can be safely accomplished with an open or Hassan, Verres needle or optical trocar if the location is adjusted according to fundal height, previous incisions, and experience of the surgeon (Level III, Grade B).

Nuclear Medicine Guideline 5: Nuclear medicine administration of radionucleotides can generally be accomplished at fetal radiation levels of exposure that are well below any known detrimental levels (Level III, Grade C).

Insufation Pressure Cholangiography Guideline 6: Intraoperative and endoscopic cholangiography exposes the mother and fetus to minimal Guideline 12: CO2 insufation of 1015 mmHg can be safely used for laparoscopy in the pregnant patient. Intra-abdominal pressure should be sufcient to allow for adequate visualization (Level III, Grade C).

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Intraoperative CO2 Monitoring Guideline 13: Intraoperative CO2 monitoring by capnography should be used during laparoscopy in the pregnant patient (Level III, Grade C). Venous Thromboembolic (VTE) Prophylaxis Guideline 14: Intraoperative and postoperative pneumatic compression devices and early postoperative ambulation are recommended prophylaxis for deep venous thrombosis in the gravid patient (Level III, Grade C). Gallbladder Disease Guideline 15: Laparoscopic cholecystectomy is the treatment of choice in the pregnant patient with gallbladder disease regardless of trimester (Level II, Grade B). Choledocholithiasis

Observation is acceptable for all other cystic lesions provided ultrasound is non-worrisome for malignancy and tumor markers are normal. Initial observation is warranted for most cystic lesions \6 cm in size (Level III, Grade C).

Adnexal Torsion Guideline 20: Laparoscopy is recommended for both diagnosis and treatment of adnexal torsion unless clinical severity warrants laparotomy (Level III, Grade C).

Perioperative care Fetal Heart Monitoring Guideline 21: Fetal heart monitoring should occur preand postoperatively in the setting of urgent abdominal surgery during pregnancy (Level III, Grade B).

Obstetrical Consultation Guideline 16: Choledocholithiasis during pregnancy may be managed with preoperative endoscopic retrograde cholangiopancreatography (ERCP) with sphincterotomy followed by laparoscopic cholecystectomy, intraoperative laparoscopic transcystic or choledochotomy common bile duct exploration, or postoperative ERCP depending on local resources and clinical scenario (Level III, Grade C). Guideline 22: Obstetric consultation can be obtained pre- and/or postoperatively based on the acuteness of the patients disease and availability (Level III, Grade B).

Tocolytics Guideline 23: Tocolytics should not be used prophylactically, but should be considered perioperatively when signs of preterm labor are present in coordination with obstetric consultation (Level I, Grade A).

Laparoscopic Appendectomy Guideline 17: Laparoscopic appendectomy may be performed safely in any patients with suspicion of appendicitis (Level II, Grade B).

Appendix A: Levels of Evidence Solid Organ Resection Guideline 18: Laparoscopic adrenalectomy, nephrectomy, splenectomy and mesenteric cyst excision are safe procedures in pregnant patients when indicated and standard precautions are taken (Level III, Grade C).

Level 1 Evidence from properly conducted randomized, controlled trials Level II Evidence from controlled trials without randomization Or Cohort or case-control studies Or Level III Multiple time series, dramatic uncontrolled experiments Descriptive case series, opinions of expert panels

Adnexal Mass Guideline 19: Laparoscopy is safe and effective treatment in gravid patients with symptomatic cystic masses.

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Surg Endosc (2008) 22:849861 20. Forsted DH, Kalbhen CL (2002) CT of pregnant women for urinary tract calculi, pulmonary thromboembolism, and acute appendicitis. AJR Am J Roentgenol 178(5):1285 21. De Wilde JP, Rivers AW, Price DL (2005) A review of the current use of magnetic resonance imaging in pregnancy and safety implications for the fetus. Prog Biophys Mol Biol 87(2 3):33553 22. Garcia-Bournissen F, Shrim A, Koren G (2006) Safety of gadolinium during pregnancy. Can Fam Physician 52:30910 23. Nagayama M et al (2002) Fast MR imaging in obstetrics. Radiographics 22(3):56380; discussion 5802 24. Leyendecker JR, Gorengaut V, Brown JJ (2004) MR imaging of maternal diseases of the abdomen and pelvis during pregnancy and the immediate postpartum period. Radiographics 24(5): 130116 25. McKenna DA et al (2007) The use of MRI to demonstrate small bowel obstruction during pregnancy. Br J Radiol 80(949):e114 26. Adelstein SJ (1999) Administered radionuclides in pregnancy. Teratology 59(4):2369 27. Andriulli A et al (2007) Incidence rates of post-ERCP complications: A systematic survey of prospective studies. Am J Gastroenterol 102(8):17818 28. Qureshi WA et al (2005) ASGE guideline: Guidelines for endoscopy in pregnant and lactating women. Gastrointest Endosc 61(3):35762 29. Quan WL, Chia CK, Yim HB (2006) Safety of endoscopical procedures during pregnancy. Singapore Med J 47(6):5258 30. Reedy MB, Kallen B, Kuehl TJ (1997) Laparoscopy during pregnancy: a study of ve fetal outcome parameters with use of the Swedish Health Registry. Am J Obstet Gynecol 177(3):6739 31. Reedy MB et al (1997) Laparoscopy during pregnancy. A survey of laparoendoscopic surgeons. J Reprod Med 42(1):338 32. Gurbuz AT, Peetz ME (1997) The acute abdomen in the pregnant patient. Is there a role for laparoscopy? Surg Endosc 11(2):98102 33. Buser KB (2002) Laparoscopic surgery in the pregnant patientone surgeons experience in a small rural hospital. JSLS 6(2):1214 34. Lachman E et al (1999) Pregnancy and laparoscopic surgery. J Am Assoc Gynecol Laparosc 6(3):34751 35. Fatum M, Rojansky N (2001) Laparoscopic surgery during pregnancy. Obstet Gynecol Surv 56(1):509 36. Curet MJ et al (1996) Laparoscopy during pregnancy. Arch Surg 131(5):54650; discussion 5501 37. Conron RW Jr et al (1999) Laparoscopic procedures in pregnancy. Am Surg 65(3):25963 38. Al-Fozan H, Tulandi T (2002) Safety and risks of laparoscopy in pregnancy. Curr Opin Obstet Gynecol 14(4):3759 39. Amos JD et al (1996) Laparoscopic surgery during pregnancy. Am J Surg 171(4):4357 40. Nezhat FR et al (1997) Laparoscopy during pregnancy: a literature review. JSLS 1(1):1727 41. Guidelines for laparoscopic surgery during pregnancy (1998) Surg Endosc 12(2):18990 42. Rizzo AG (2003) Laparoscopic surgery in pregnancy: long-term follow-up. J Laparoendosc Adv Surg Tech A 13(1):115 43. Andreoli M et al (1999) Laparoscopic surgery during pregnancy. J Am Assoc Gynecol Laparosc 6(2):22933 44. Shay DC, Bhavani-Shankar K, Datta S (2001) Laparoscopic surgery during pregnancy. Anesthesiol Clin North Am 19(1): 5767 45. Oelsner G et al (2003) Pregnancy outcome after laparoscopy or laparotomy in pregnancy. J Am Assoc Gynecol Laparosc 10(2):2004 46. Oelsner G et al (2003) Pregnancy outcome after laparoscopy or laparotomy in pregnancy. J Am Assoc Gynecol Laparosc 10(2):2004

Appendix B: Scale for Evidence Grading

Grade A Grade B Grade C

High-level (level I or II), well-performed studies with uniform interpretation and conclusions by the expert panel High-level, well-performed studies with varying interpretation and conclusions by the expert panel Lower-level evidence (level II or less) with inconsistent ndings and/or varying interpretations or conclusions by the expert panel

References
1. Kammerer WS (1979) Nonobstetric surgery during pregnancy. Med Clin North Am 63(6):115764 2. Kort B, Katz VL, Watson WJ (1993) The effect of nonobstetric operation during pregnancy. Surg Gynecol Obstet 177(4):3716 3. Fallon WF Jr et al (1995) The surgical management of intraabdominal inammatory conditions during pregnancy. Surg Clin North Am 75(1):1531 4. Baer J (1932) Appendicitis in pregnancy with changes in position and axis of the normal appendix in pregnancy. JAMA 98:13591364 5. Eyvazzadeh AD, D Levine (2006) Imaging of pelvic pain in the rst trimester of pregnancy. Radiol Clin North Am 44(6): 86377 6. Medical radiation exposure of pregnant and potentially pregnant women. 1977, National Council on Radiation Protection and Measurements report no. 54: Bethesda, MD 7. Kennedy A (2000) Assessment of acute abdominal pain in the pregnant patient. Semin Ultrasound CT MR 21(1):6477 8. Toppenberg KS, Hill DA, Miller DP, Safety of radiographic imaging during pregnancy. Am Fam Physician 59(7):18138, 1820 9. Moore C, Promes SB (2004) Ultrasound in pregnancy. Emerg Med Clin North Am 22(3):697722 10. Lim HK, Bae SH, Seo GS (1992) Diagnosis of acute appendicitis in pregnant women: value of sonography. AJR Am J Roentgenol 159(3):53942 11. Nelson MJ et al (1986) Cysts in pregnancy discovered by sonography. J Clin Ultrasound 14(7):50912 12. Timins JK (2001) Radiation during pregnancy. N J Med 98(6):2933 13. Karam PA (2000) Determining and reporting fetal radiation exposure from diagnostic radiation. Health Phys 79(5 Suppl):S8590 14. Medical radiation exposure of pregnant and potentially pregnant women. National Council on Radiation Protection and Measurements report No. 54: Bethesda, MD., 1977 15. Doll R, Wakeford R (1997) Risk of childhood cancer from fetal irradiation. Br J Radiol 70:1309 16. Osei EK, Faulkner K (1999) Fetal doses from radiological examinations. Br J Radiol 72(860):77380 17. Lowe SA (2004) Diagnostic radiography in pregnancy: risks and reality. Aust N Z J Obstet Gynaecol 44(3):1916 18. Menias CO et al (2007) CT of pregnancy-related complications. Emerg Radiol 13(6):299306 19. Hurwitz LM et al (2006) Radiation dose to the fetus from body MDCT during early gestation. AJR Am J Roentgenol 186(3): 8716

123

Surg Endosc (2008) 22:849861 47. McKellar DP et al (1992) Cholecystectomy during pregnancy without fetal loss. Surg Gynecol Obstet 174(6):4658 48. Glasgow RE et al (1998) Changing management of gallstone disease during pregnancy. Surg Endosc 12(3):2416 49. Afeck DG et al (1999) The laparoscopic management of appendicitis and cholelithiasis during pregnancy. Am J Surg 178(6):5239 50. Barone JE et al (1999) Outcome study of cholecystectomy during pregnancy. Am J Surg 177(3):2326 51. Rollins MD, Chan KJ, Price RR (2004) Laparoscopy for appendicitis and cholelithiasis during pregnancy: a new standard of care. Surg Endosc 18(2):23741 52. Davis A, Katz VL, Cox R (1995) Gallbladder disease in pregnancy. J Reprod Med 40(11):75962 53. Muench J et al (2001) Delay in treatment of biliary disease during pregnancy increases morbidity and can be avoided with safe laparoscopic cholecystectomy. Am Surg 67(6):53942; discussion 5423 54. Visser BC et al (2001) Safety and timing of nonobstetric abdominal surgery in pregnancy. Dig Surg 18(5):40917 55. Geisler JP et al (1998) Non-gynecologic laparoscopy in second and third trimester pregnancy: obstetric implications. JSLS 2(3):2358 56. Stepp K, Falcone T (2004) Laparoscopy in the second trimester of pregnancy. Obstet Gynecol Clin North Am 31(3):48596, vii 57. Pucci RO, Seed RW (1991) Case report of laparoscopic cholecystectomy in the third trimester of pregnancy. Am J Obstet Gynecol 165(2):4012 58. Weber AM et al (1991) Laparoscopic cholecystectomy during pregnancy. Obstet Gynecol 78(5 Pt 2):9589 59. Williams JK et al (1995) Laparoscopic cholecystectomy in pregnancy. A case report. J Reprod Med 40(3):2435 60. Arvidsson D, Gerdin E (1991) Laparoscopic cholecystectomy during pregnancy. Surg Laparosc Endosc 1(3):1934 61. Costantino GN et al (1994) Laparoscopic cholecystectomy in pregnancy. J Laparoendosc Surg 4(2):1614 62. Soriano D et al (1999) Laparoscopy versus laparotomy in the management of adnexal masses during pregnancy. Fertil Steril 71(5):95560 63. Curet MJ (2000) Special problems in laparoscopic surgery. Previous abdominal surgery, obesity, and pregnancy. Surg Clin North Am 80(4):1093110 64. Elkayam GNU (1982) Cardiovascular physiology of pregnancy. Cardiac Problems in Pregnancy: Diagnosis and Management of Maternal and Fetal Disease, ed. Elkayam GNU. New York, NY: Alan R Liss. 5 65. Clark SL et al (1991) Position change and central hemodynamic prole during normal third-trimester pregnancy and post partum. Am J Obstet Gynecol 164(3):8837 66. Gordon MC (2002) Maternal Physiology in Pregnancy, in Obstetrics: Normal and Problem Pregnancies, Gabbe SG, Niebyl JR, Simpson JL, eds. 2002, Churchill Livingstone: Philadelphia, pp. 6391 67. Friedman JD et al (2002) Pneumoamnion and pregnancy loss after second-trimester laparoscopic surgery. Obstet Gynecol 99(3):5123 68. Halpern NB (1998) Laparoscopic cholecystectomy in pregnancy: a review of published experiences and clinical considerations. Semin Laparosc Surg 5(2):12934 69. Lemaire BM, van Erp WF (1997) Laparoscopic surgery during pregnancy. Surg Endosc 11(1):158 70. Canis M et al (2002) Laparoscopic management of adnexal masses: a gold standard? Curr Opin Obstet Gynecol 14(4):4238 71. Malangoni MA (2003) Gastrointestinal surgery and pregnancy. Gastroenterol Clin North Am 32(1):181200

859 72. Wang CJ et al (2002) Minilaparoscopic cystectomy and appendectomy in late second trimester. JSLS 6(4):3735 73. Akira S et al (1999) Gasless laparoscopic ovarian cystectomy during pregnancy: comparison with laparotomy. Am J Obstet Gynecol 180(3 Pt 1):5547 74. Murakami T et al (2003) Cul-de-sac packing with a metreurynter in gasless laparoscopic cystectomy during pregnancy. J Am Assoc Gynecol Laparosc 10(3):4213 75. Schmidt T et al (2001) Gasless laparoscopy as an option for conservative therapy of adnexal pedical torsion with twin pregnancy. J Am Assoc Gynecol Laparosc 8(4):6212 76. Romer T, Bojahr B, Schwesinger G (2002) Treatment of a torqued hematosalpinx in the thirteenth week of pregnancy using gasless laparoscopy. J Am Assoc Gynecol Laparosc 9(1): 8992 77. Melgrati L et al (2005) Isobaric (gasless) laparoscopic myomectomy during pregnancy. J Minim Invasive Gynecol 12(4): 37981 78. Matsumoto T et al (1999) Laparoscopic treatment of uterine prolapse during pregnancy. Obstet Gynecol 93(5 Pt 2):849 79. Oguri H, Taniguchi K, Fukaya T (2005) Gasless laparoscopic management of ovarian cysts during pregnancy. Int J Gynaecol Obstet 91(3):2589 80. Iafrati MD, Yarnell R, Schwaitzberg SD (1995) Gasless laparoscopic cholecystectomy in pregnancy. J Laparoendosc Surg 5(2):12730 81. Hume RF, Killiam AP (1990) Maternal Physiology, in Obstetrics and Gynecology, Scott JR, KiSaia J, Hammon DB, eds. JB Lippincott: Philadelphia. pp. 93100 82. Guidelines for laparoscopic surgery during pregnancy (1998) Society of American Gastrointestinal Endoscopic Surgeons (SAGES). Surg Endosc 12(2):18990 83. Hunter JG, Swanstrom L, Thornburg K (1995) Carbon dioxide pneumoperitoneum induces fetal acidosis in a pregnant ewe model. Surg Endosc 9(3):2727; discussion 2779 84. Reedy MB et al (1995) Maternal and fetal effects of laparoscopic insufation in the gravid baboon. J Am Assoc Gynecol Laparosc 2(4):399406 85. Curet MJ et al (1996) Effects of CO2 pneumoperitoneum in pregnant ewes. J Surg Res 63(1):33944 86. Barnard JM et al (1995) Fetal response to carbon dioxide pneumoperitoneum in the pregnant ewe. Obstet Gynecol 85(5 Pt 1):66974 87. Cruz AM et al (1996) Intraabdominal carbon dioxide insufation in the pregnant ewe. Uterine blood ow, intraamniotic pressure, and cardiopulmonary effects. Anesthesiology 85(6): 1395402 88. Soper NJ, Hunter JG, Petrie RH (1992) Laparoscopic cholecystectomy during pregnancy. Surg Endosc 6(3):1157 89. Comitalo JB, Lynch D (1994) Laparoscopic cholecystectomy in the pregnant patient. Surg Laparosc Endosc 4(4):26871 90. Bhavani-Shankar K et al (2000) Arterial to end-tidal carbon dioxide pressure difference during laparoscopic surgery in pregnancy. Anesthesiology 93(2):3703 91. Melnick DM, Wahl WL, Dalton VK (2004) Management of general surgical problems in the pregnant patient. Am J Surg 187(2):17080 92. Jorgensen JO et al (1994) Venous stasis during laparoscopic cholecystectomy. Surg Laparosc Endosc 4(2):12833 93. Risk of and prophylaxis for venous thromboembolism in hospital patients (1992) Thromboembolic Risk Factors (THRIFT) Consensus Group. BMJ 305(6853):56774 94. Casele HL (2006) The use of unfractionated heparin and low molecular weight heparins in pregnancy. Clin Obstet Gynecol 49(4):895905

123

860 95. Hiatt JR et al (1986) Biliary disease in pregnancy: strategy for surgical management. Am J Surg 151(2):2635 96. Ghumman E, Barry M, Grace PA (1997) Management of gallstones in pregnancy. Br J Surg 84(12):164650 97. Chamogeorgakis T et al (1999) Laparoscopic cholecystectomy during pregnancy: three case reports. JSLS 3(1):679 98. Steinbrook RA, Brooks DC, Datta S (1996) Laparoscopic cholecystectomy during pregnancy. Review of anesthetic management, surgical considerations. Surg Endosc 10(5):5115 99. Scott LD (1992) Gallstone disease and pancreatitis in pregnancy. Gastroenterol Clin North Am 21(4):80315 100. Printen KJ, Ott RA (1978) Cholecystectomy during pregnancy. Am Surg 44(7):4324 101. Graham G, Baxi L, Tharakan T (1998) Laparoscopic cholecystectomy during pregnancy: a case series and review of the literature. Obstet Gynecol Surv 53(9):56674 102. DeVore GR (1980) Acute abdominal pain in the pregnant patient due to pancreatitis, acute appendicitis, cholecystitis, or peptic ulcer disease. Clin Perinatol 7(2):34969 103. Borum ML (1998) Hepatobiliary diseases in women. Med Clin North Am 82(1):5175 104. Tuech JJ et al (2000) Management of choledocholithiasis during pregnancy by magnetic resonance cholangiography and laparoscopic common bile duct stone extraction. Surg Laparosc Endosc Percutan Tech 10(5):3235 105. Baillie J et al (1990) Endoscopic management of choledocholithiasis during pregnancy. Surg Gynecol Obstet 171(1):14 106. Sungler P et al (2000) Laparoscopic cholecystectomy and interventional endoscopy for gallstone complications during pregnancy. Surg Endosc 14(3):26771 107. Cosenza CA et al (1999) Surgical management of biliary gallstone disease during pregnancy. Am J Surg 178(6):5458 108. Barthel JS, Chowdhury T, Miedema BW (1998) Endoscopic sphincterotomy for the treatment of gallstone pancreatitis during pregnancy. Surg Endosc 12(5):3949 109. Scapa E (1995) To do or not to do an endoscopic retrograde cholangiopancreatography in acute biliary pancreatitis? Surg Laparosc Endosc 5(6):4534 110. Andreoli M et al (1996) Laparoscopic cholecystectomy for recurrent gallstone pancreatitis during pregnancy. South Med J 89(11):11145 111. Schwartzberg BS, Conyers JA, Moore JA (1997) First trimester of pregnancy laparoscopic procedures. Surg Endosc 11(12):12167 112. Thomas SJ, Brisson P (1998) Laparoscopic appendectomy and cholecystectomy during pregnancy: Six case reports. JSLS 2(1):416 113. Barnes SL et al (2004) Laparoscopic appendectomy after 30 weeks pregnancy: Report of two cases and description of technique. Am Surg 70(8):7336 114. de Perrot M et al (2000) Laparoscopic appendectomy during pregnancy. Surg Laparosc Endosc Percutan Tech 10(6):36871 115. Schreiber JH (1990) Laparoscopic appendectomy in pregnancy. Surg Endosc 4(2):1002 116. Mazze RI, Kallen B (1991) Appendectomy during pregnancy: a Swedish registry study of 778 cases. Obstet Gynecol 77(6): 83540 117. Cunningham FG, McCubbin JH (1975) Appendicitis complicating pregnancy. Obstet Gynecol 45(4):41520 118. Andersen B, Nielsen TF (1999) Appendicitis in pregnancy: diagnosis, management and complications. Acta Obstet Gynecol Scand 78(9):75862 119. Horowitz MD et al (1985) Acute appendicitis during pregnancy. Diagnosis and management. Arch Surg 120(12):13627 120. Mourad J et al (2000) Appendicitis in pregnancy: new information that contradicts long-held clinical beliefs. Am J Obstet Gynecol 182(5):10279

Surg Endosc (2008) 22:849861 121. Mahmoodian S (1992) Appendicitis complicating pregnancy. South Med J 85(1):1924 122. Cappell MS, Friedel D (2003) Abdominal pain during pregnancy. Gastroenterol Clin North Am 32(1):158 123. Tamir IL, Bongard FS, Klein SR (1990) Acute appendicitis in the pregnant patient. Am J Surg 160(6):5715; discussion 5756 124. Weingold AB (1983) Appendicitis in pregnancy. Clin Obstet Gynecol 26(4):8019 125. Shalhav AL et al (2000) Laparoscopic adrenalectomy for primary hyperaldosteronism during pregnancy. J Laparoendosc Adv Surg Tech A 10(3):16971 126. Finkenstedt G et al (1999) Pheochromocytoma and sub-clinical Cushings syndrome during pregnancy: diagnosis, medical pretreatment and cure by laparoscopic unilateral adrenalectomy. J Endocrinol Invest 22(7):5517 127. Aishima M et al (2000) Retroperitoneal laparoscopic adrenalectomy in a pregnant woman with Cushings syndrome. J Urol 164(3 Pt 1):7701 128. Lo CY, Lo CM, Lam KY (2002) Cushings syndrome secondary to adrenal adenoma during pregnancy. Surg Endosc 16(1):21920 129. Janetschek G et al (1998) Laparoscopic surgery for pheochromocytoma: adrenalectomy, partial resection, excision of paragangliomas. J Urol 160(2):3304 130. Demeure MJ et al (1998) Laparoscopic removal of a right adrenal pheochromocytoma in a pregnant woman. J Laparoendosc Adv Surg Tech A 8(5):3159 131. Pace DE et al (2002) Minimally invasive adrenalectomy for pheochromocytoma during pregnancy. Surg Laparosc Endosc Percutan Tech 12(2):1225 132. Gagner M et al (1996) Is laparoscopic adrenalectomy indicated for pheochromocytomas? Surgery 120(6):10769; discussion 107980 133. Wolf A et al (2004) Pheochromocytoma during pregnancy: laparoscopic and conventional surgical treatment of two cases. Exp Clin Endocrinol Diabetes 112(2):98101 134. Kim PT et al (2006) Laparoscopic adrenalectomy for pheochromocytoma in pregnancy. Can J Surg 49(1):623 135. Grifths J et al (2005) Laparoscopic splenectomy for the treatment of refractory immune thrombocytopenia in pregnancy. J Obstet Gynaecol Can 27(8):7714 136. Hardwick RH et al (1999) Laparoscopic splenectomy in pregnancy. J Laparoendosc Adv Surg Tech A 9(5):43940 137. Allran CF Jr., Weiss CA 3rd, Park AE (2002) Urgent laparoscopic splenectomy in a morbidly obese pregnant woman: Case report and literature review. J Laparoendosc Adv Surg Tech A 12(6):4457 138. Iwase K et al (2001) Hand-assisted laparoscopic splenectomy for idiopathic thrombocytopenic purpura during pregnancy. Surg Laparosc Endosc Percutan Tech 11(1):536 139. Anglin BV et al (2001) Immune thrombocytopenic purpura during pregnancy: laparoscopic treatment. JSLS 5(1):637 140. OConnor JP et al (2004) Laparoscopic nephrectomy for renalcell carcinoma during pregnancy. J Endourol 18(9):8714 141. Sainsbury DC et al (2004) Laparoscopic radical nephrectomy in rst-trimester pregnancy. Urology 64(6):1231 e78 142. Bozzo M, Buscaglia M, Ferrazzi E (1997) The management of persistent adnexal masses in pregnancy. Am J Obstet Gynecol 177(4):9812 143. Thornton JG, Wells M (1987) Ovarian cysts in pregnancy: does ultrasound make traditional management inappropriate? Obstet Gynecol 69(5):71721 144. Grimes WH Jr et al (1954) Ovarian cyst complicating pregnancy. Am J Obstet Gynecol 68(2):594605 145. Sherard GB 3rd et al (2003) Adnexal masses and pregnancy: a 12year experience. Am J Obstet Gynecol 189(2):35862; discussion 3623

123

Surg Endosc (2008) 22:849861 146. Hess LW et al (1988) Adnexal mass occurring with intrauterine pregnancy: report of fty-four patients requiring laparotomy for denitive management. Am J Obstet Gynecol 158(5):102934 147. Schmeler KM et al (2005) Adnexal masses in pregnancy: surgery compared with observation. Obstet Gynecol 105(5 Pt 1): 1098103 148. Zanetta G et al (2003)A prospective study of the role of ultrasound in the management of adnexal masses in pregnancy. BJOG 110(6):57883 149. Condous G et al (2004) Should we be examining the ovaries in pregnancy? Prevalence and natural history of adnexal pathology detected at rst-trimester sonography. Ultrasound Obstet Gynecol 24(1):626 150. ACOG Practice Bulletin (2007) Management of adnexal masses. Obstet Gynecol 110(1):20114 151. Nezhat F et al (1991) Laparoscopic ovarian cystectomy during pregnancy. J Laparoendosc Surg 1(3):1614 152. Parker WH et al (1994) A multicenter study of laparoscopic management of selected cystic adnexal masses in postmenopausal women. J Am Coll Surg 179(6):7337 153. Tazuke SI et al (1997) Laparoscopic management of pelvic pathology during pregnancy. J Am Assoc Gynecol Laparosc 4(5):6058 154. Chung MK, Chung RP (2001) Laparoscopic extracorporeal oophorectomy and ovarian cystectomy in second trimester pregnant obese patients. JSLS 5(3):2737 155. Yuen PM, Chang AM (1997) Laparoscopic management of adnexal mass during pregnancy. Acta Obstet Gynecol Scand 76(2):1736 156. Loh FH et al (1998) Case report of ruptured endometriotic cyst in pregnancy treated by laparoscopic ovarian cystectomy. Singapore Med J 39(8):3689 157. Stepp KJ et al (2003) Laparoscopy for adnexal masses in the second trimester of pregnancy. J Am Assoc Gynecol Laparosc 10(1):559 158. Neiswender LL, Toub DB (1997) Laparoscopic excision of pelvic masses during pregnancy. J Am Assoc Gynecol Laparosc 4(2):26972 159. Yuen PM et al (2004) Outcome in laparoscopic management of persistent adnexal mass during the second trimester of pregnancy. Surg Endosc 18(9):13547 160. Parker J et al (1995) Laparoscopic adnexal surgery during pregnancy: a case of heterotopic tubal pregnancy treated by laparoscopic salpingectomy. Aust N Z J Obstet Gynaecol 35(2): 20810 161. Moore RD, Smith WG (1999) Laparoscopic management of adnexal masses in pregnant women. J Reprod Med 44(2):97100

861 162. Lin YH et al (2003) Successful laparoscopic management of a huge ovarian tumor in the 27th week of pregnancy. A case report. J Reprod Med 48(10):8346 163. Mathevet P et al (2003) Laparoscopic management of adnexal masses in pregnancy: a case series. Eur J Obstet Gynecol Reprod Biol 108(2):21722 164. Struyk AP, Treffers PE (1984) Ovarian tumors in pregnancy. Acta Obstet Gynecol Scand 63(5):4214 165. Nichols DH, Julian PJ (1985) Torsion of the adnexa. Clin Obstet Gynecol 28(2):37580 166. Mage G et al (1989) Laparoscopic management of adnexal torsion. A review of 35 cases. J Reprod Med 34(8):5204 167. Garzarelli S, Mazzuca N (1994) One laparoscopic puncture for treatment of ovarian cysts with adnexal torsion in early pregnancy. A report of two cases. J Reprod Med 39(12):9856 168. Morice P et al (1997) Laparoscopy for adnexal torsion in pregnant women. J Reprod Med 42(7):4359 169. Abu-Musa A et al (2001) Laparoscopic unwinding and cystectomy of twisted dermoid cyst during second trimester of pregnancy. J Am Assoc Gynecol Laparosc 8(3):45660 170. Bassil S, Steinhart U, Donnez J (1999) Successful laparoscopic management of adnexal torsion during week 25 of a twin pregnancy. Hum Reprod 14(3):8557 171. Argenta PA et al (2000) Torsion of the uterine adnexa. Pathologic correlations and current management trends. J Reprod Med 45(10):8316 172. Tarraza HM, Moore RD (1997) Gynecologic causes of the acute abdomen and the acute abdomen in pregnancy. Surg Clin North Am 77(6):137194 173. Oelsner G et al (1993) Long-term follow-up of the twisted ischemic adnexa managed by detorsion. Fertil Steril 60(6): 9769 174. Sharp HT (2002) The acute abdomen during pregnancy. Clin Obstet Gynecol 45(2):40513 175. Katz VL, Farmer RM (1999) Controversies in tocolytic therapy. Clin Obstet Gynecol 42(4):80219 176. Berkman ND et al (2003) Tocolytic treatment for the management of preterm labor: a review of the evidence. Am J Obstet Gynecol 188(6):164859 177. Tan TC et al (2006) Tocolytic treatment for the management of preterm labour: a systematic review. Singapore Med J 47(5):3616 178. Romero R et al (2000) An oxytocin receptor antagonist (atosiban) in the treatment of preterm labor: a randomized, doubleblind, placebo-controlled trial with tocolytic rescue. Am J Obstet Gynecol 182(5):117383

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