Epidemiology
about 1% of pregnant females undergo non-obstetric surgery
most commonly appendectomy & cholecystectomy
Diagnosis & Workup: early & accurate diagnosis begets a better prognosis
US: ultrasound during pregnancy is safe & effective in identifying the etiology of acute abdominal pain in many patients & should be the initial imaging test of choice
best initial test for most Ob/Gyn causes of abd pain (i.e., adnexal mass, ovarian torsion, placental abruption, placenta previa, uterine rupture, & fetal demise) for which it is up to 80% sensitive & 94% specific
also useful for many non-Ob/Gyn causes of abd pain (i.e., symptomatic cholelithiasis, appendicitis)
study of choice for biliary pathology, > 90% accurate
visualizes appendix in up to 60% of pregnancies with RLQ pain
CT: abdominal & pelvic CT scan may be used in emergency situations during pregnancy but should not be the initial imaging test of choice
consider CT only when US is non-diagnostic & MRI is unavailable or inexpedient (i.e., trauma)
ionizing radiation exposure to the fetus increases the risk of teratogenesis & childhood leukemia
cumulative dosage during pregnancy should be limited to 50-100 mGy; for example:
KUB: 1-3 mGy
IOC: 2 mGy
L-spine XR: 6 mGy
IV pyleogram: 6 mGy
barium enema: 7 mGy
CT abdomen & pelvis: 20-50 mGy
ERCP (w/out pelvic shielding): 20-120 mGy
fetal age at exposure is important, where fetal mortality is greatest when exposure occurs w/in the 1st week of conception
most sensitive time period for CNS teratogenesis is 10-17 weeks EGA
in later pregnancy, concern shifts away from teratogenesis to increasing the risk of childhood hematologic malignancy
background incidence is 0.2-0.3%
every 10 mGy increases this by 0.06%
> 99% of fetuses are unaffected by cumulative dosage < 20 mGy
risk of teratogenesis is low when dosage is < 50 mGy
risk of malformation is significantly increased at doses > 150 mGy
MRI: non-contrasted MRI can be performed at any stage of pregnancy & is preferred over CT
gadolinium agents cross the placenta & may cause teratogenesis
in non-trauma emergencies, MRI demonstrates equivalent-to-better accuracy in diagnosing vs CT or US
nuclear medicine: administration of radionucleotides for diagnostic studies is safe for mother & fetus
radiopharmaceuticals can be administered at doses that provide whole fetal exposure of < 5 mGy
cholangiography: IOC & ERCP expose mother & fetus to minimal radiation & may be used selectively during pregnancy, but the lower abdomen should be shielded to decrease the exposure
without compromising the field of view necessary for proper imaging, shield the fetus as able
ERCP radiation exposure can be substantially higher for long procedures, not to mention risk of bleeding & pancreatitis
consider EUS & choledochoscopy as able
diagnostic laparoscopy: in the absence of access to imaging modalities or non-diagnostic imaging, laparoscopy may be used selectively
accurate & timely diagnosis of abdominal conditions during pregnancy optimizes maternal & fetal outcomes
risks of delayed diagnosis should be weighed against the risk of possible negative laparoscopy
Therapy
timing
laparoscopy is safe during any trimester without an increased risk to the mother & fetus
postponing necessary operations until after parturition increases complications for both mother & fetus
positioning
2nd-3rd trimester pregnancies should be placed in partial LLDP to minimize vena cava compression
decreased venous return increases maternal hypotension & decreases placental perfusion
1st trimester does not require altered positioning
port placement
open & closed abdominal entry techniques are safe when performed by an experienced surgeon
initial port placement should be subcostal to avoid the uterus
port placement should be adjusted according to fundal height
insufflation & CO2 monitoring
insufflation to 10-15 mmHg is generally safe in pregnancy, but it should be adjusted according to patient physiology
there is theoretical concern that intraperitoneal CO2 exchange from CO2 pneumoperitoneum can have deleterious effects to the fetus
animal studies show conflicting findings
no data has shown detrimental effects to human fetuses
capnography during laparoscopy can serve as a surrogate to monitor fetal acidosis
VTE PPX
pregnancy is a hypercoagulable state with a 0.1-0.2% incidence of DVT
all patients should have pneumatic compression & early post-op ambulation
LMWHs & UFH are safe & should be used when indicated (i.e. Caprini score > 4)
gallbladder disease
early surgical management is the treatment of choice
in patients managed non-op, symptomatic cholelithiasis recurs in 92% (if 1st trimester), 64% (2nd trimester), & 44% (3rd trimester)
if deciding to manage non-operatively, there is no significant difference in the rates of preterm labor and spontaneous abortion if biliary disease remains uncomplicated
50% of recurrent symptomatic cholelithiasis requires hospitalization because up to 23% of such patients develop acute cholecystitis, cholangitis, or gallstone pancreatitis
complicated gallstone disease poses a 20% risk of preterm labor & 10-60% risk of fetal loss
choledocholithiasis
cholangitis post a 10% risk of preterm labor or spontaneous abortion
both ERCP and laparoscopic CBD exploration are safe in pregnancy
laparoscopic appendectomy
retrospective data from 1995-2002 suggests that complicated appendicitis carries a 6% risk of fetal loss & 11% chance of preterm labor (vs 2% and 4% when uncomplicated)
evidence for the use of antibiotics alone for treating uncomplicated appendicitis has not been extended to pregnancy
lap appy is the treatment of choice for pregnant patients w/acute appendicitis
other conditions
laparoscopic adrenalectomy, nephrectomy & splenectomy are safe procedures in appropriately selected pregnant patients
laparoscopy is a safe & effective in gravid patients w/symptomatic ovarian cystic masses
observation is acceptable for all other ovarian cystic lesions provided no concerning features for malignancy
laparoscopy is recommended for both diagnosis & treatment of adnexal torsion
Peri-Op Monitoring
fetal heart monitoring
pre-op & post-op FHR monitoring should be performed for all viable pregnancies (i.e., 22-24 weeks EGA)
tocolytics
tocolytics should not be used prophylactically when undergoing surgery
only consider tocolytics when signs of preterm labor are present
Resources
Pearl, Jonathan P., et al. Guidelines for the Use of Laparoscopy During Pregnancy. Society of American Gastrointestinal and Endoscopic Surgeons, May 2017.