Imaging non-obstetrical causes of abdominal pain in the pregnant patient.
The choices for imaging the acute pregnant abdomen can include plain radiographs, ultrasound, non-contrast computed tomography (CT), contrast-enhanced CT, non-contrast magnetic resonance imaging (MRI) and contrast-enhanced MRI. For the most part, excretory urography and barium gastrointestinal studies are rarely, if ever, utilized.
The American College of Radiology (ACR) recommends that when performing imaging for evaluation of the pregnant woman, non-ionizing techniques, such as sonography and MRI should be used as the first choice. (1,2) As the precise clinical etiology of abdominal pain is usually not known, there would be little argument against use of sonography in any pregnant patient with abdominal pain (Figure 1). For instance, while acute appendicitis may be clinically suspected, ovarian torsion may be detected. While ultrasound may be more sensitive to the patient in the first trimester, the use of ultrasound in the second and third trimesters may have less sensitivity in detection of certain conditions. In all cases, sonography should be used to document fetal viability or any pregancy complications.
Magnetic resonance imaging
MRI, like ultrasound, does not use ionizing radiation. However, unlike ultrasound, scanning with MRI is more complex due to several factors: greater exam time, patient claustrophobia, patient transport and limited after-hours access. Nevertheless, MRI utilization has been increasing in the evaluation of non-obstetrical emergencies. In pregnant patients, general MRI protocols include an MRI localizer, followed by T2weighted (T2W) single shot fast spin echo (SSFSE) multiplanar images, and multislice spoiled gradient echo techniques (Table 1).
The use of gadolinium during pregnancy is much more controversial. Gadolinium dimeglumine in pregnancy is classified as a C-class drug. This classification includes drugs where there are no well-controlled studies in pregnant women, however, animal studies have shown adverse effects. (3) Maternally administered gadolinium crosses the placenta and enters the fetal circulation. While gadolinium in a chelate form is harmless, the free form of gadolinium is highly toxic. The effects of gadolinium on the developing fetus have not been well studied (Table 2). Some literature advises against its use in pregnancy. (4)
[FIGURE 1 OMITTED]
There is increased concern about the utilization of ionizing radiation from CT and the associated, increased risk of cancer. This postulated risk is based on estimates derived from mathematical models and not on epidemiologic proof. The risk of developing leukemia is thought to be dose dependent and is greatest in younger patients. Also, the radiation dose from multidector CT protocols has been reported to be greater than single detector CT scanners. (5) However, with further engineering, the geometric efficiency of >64 detector array CT scanners has approached that of single slice CT. While teratogenic effects are believed to be minimal, there is a less well-defined increased risk of developing cancer that may be above the normal background risk. (6) The risk of cancer as a result of diagnostic levels of ionizing radiation on the developing fetus are unknown, but it remains prudent to minimize exposure of ionizing radiation on the developing fetus. This is important for the first trimester, during which organogenesis occurs.
[TABLE 5 OMITTED]
Minimizing fetal radiation exposure can be accomplished by modifying CT protocols, e. g. performing a single-phase CT, instead of multiphase CT, could reduce the dose proportionately. Decreasing the tube milli-Amperage will help with dose reduction--changing tube current from 340 mA to 160 mA, would reduce the effective radiation dose one-third. (6) Radiation dose reduction should be attained without deterioration in the quality of the exam. Finally, it is possible to limit the amount of fetal exposure by limiting the field of view. Radiation to the fetus from a CT of the maternal liver is primarily from Compton scatter rather than direct exposure obtained from CT of the pregnant uterus.
The fact remains: CT provides lifesaving diagnostic information when used for appropriate clinical indication. Radiation dose reduction, although prudent when appropriate, must not compromise the diagnostic outcome of a clinically relevant examination.
Use of iodinated contrast is also a concern (Tables 2 and 3). The fetus is exposed to iodinated contrast with maternal administration of contrast, as iodinated contrast crosses the placenta into the fetus. The risk of iodinated contrast is less than gadolinium chelates and has been classified a category B-class drug. These drugs show no fetal risks in animal studies, but there are no studies assessing human fetal risk. Therefore IV iodinated contrast should be used after assessment of the risk-benefit ratio. (7)
This review will concentrate on only the most common etiologies of pain in pregnant patients. A partial list of non-obstetrical causes of abdominal pain in the pregnant patient is listed in Table 4.
While often not considered, trauma tends to be the most common etiology of non-obstetrical abdominal pain in a pregnant patient. Approximately 6% to 7% of pregnant patients sustain abdominal trauma. While motor vehicle accidents are the most common etiology, pregnant patients can also be assaulted, may fall or suffer auto vs. pedestrian accidents.
Table 5 is taken from an article by Patel et al. regarding imaging in abdominal trauma. Ultrasound has 2 roles in assessing the pregnant trauma patients. (7) Ultrasound can access the abdominal trauma in the mother, and can also detect trauma to the fetus. In a publication from our institution, University of California, Davis Medical Center, ultrasound had 61% sensitivity and 94.4% specificity in diagnosing organ injury in pregnant patients with trauma. (8) The sensitivity of ultrasound in detecting organ injury or free fluid was 90% in the first trimester, but decreased in the second and third trimesters. Also, while ultrasound was sensitive in detecting free fluid in the mother with solid organ injury, it failed to detect many cases of abruptio placenta (Figure 2). (8)
[FIGURE 2 OMITTED]
Trauma in the pregnant patient is one indication for contrast-enhanced CT in pregnancy. Certainly, the radiation dose for head, neck and chest CT is minimal to the fetus. In considering abdominal CT in the trauma patient, the acuity and gravidity of the suspected injury usually would be of greater concern than potential radiation dose damage to the fetus. If CT of the abdomen is necessary, a single-phase contrast-enhanced CT should be used.
Acute appendicitis is the most common cause of non-traumatic acute abdominal pain in pregnancy and accounts for [less than or equal to] 25% of operative indications for non-obstetrical emergencies. Ultrasound should be used as the first imaging choice in the pregnant patient with right lower quadrant pain (Table 6). The diagnosis of acute appendicitis by sonography is easier in the first trimester than in later pregnancy. The sensitivity of sonography in the pregnant patient has been reported to be between 66% and 100%. This depends on the sonographic expertise at the particular institution. (9,10) In patients with right lower quadrant pain, sonography may be used for suspected appendicitis, but may instead detect other etiologies of pain, such as ovarian torsion. Findings of acute appendicitis are listed in Table 7 and illustrated in Figure 3.
MRI is increasingly being used for diagnosis of acute appendicitis, especially in the second and third trimester. MRI should be used for failed diagnosis with sonography. Both T1W and T2W sequences are performed. MRI may demonstrate the thickened appendix and associated peri-appendiceal inflammatory changes. The inflamed appendical wall appears hypointense on T1W and hyperintense on T2W images. The fluid-filled appendix is seen as hyperintense on T2W images and edematous high signal intensity T2W changes can be seen in the mesentery (Figure 4).
[TABLE 6 OMITTED]
In patients where MRI is inconclusive, or in whom MRI cannot be performed, CT can be used, if the diagnosis cannot be made clinically. CT has high sensitivity in diagnosing appendicitis and the risk of delayed diagnosis with possible perforation may outweigh the potential risk of perceived radiation-induced risks. There should be use of CT with efforts to reduce the dose.
[FIGURE 3 OMITTED]
Acute cholecystitis is the second most-common cause of the non-traumatic acute abdomen during pregnancy. Acute cholecystitis is secondary to cholelithiasis. Estrogen increases bile lithogenicity during pregnancy and increases the risk of cholelithiasis and acute cholecystitis. Two other consequences of cholelithiasis are choledocholithiasis and biliary (gallstone) pancreatitis.
[FIGURE 4 OMITTED]
[TABLE 8 OMITTED]
[FIGURE 5 OMITTED]
[FIGURE 6 OMITTED]
Ultrasound is the initial study of choice in diagnosing cholelithiasis and acute cholecystitis (Table 8). Diagnosis by ultrasound includes testing for the presence of gallstones and a positive ultrasonic Murphy's sign. Wall thickening, pericholecystic fluid collections and gallbladder striations are other useful signs (Figures 5 and 6). Laparoscopic management of acute cholecystitis is used if medical management fails. Ultrasound has been used to guide percutaneous cholecystostomy in pregnant patients to temporize acute cholecystitis with cholecystostomy delayed until after birth (Figure 7). (11)
[FIGURE 7 OMITTED]
Depending on the patient's symptoms, magnetic resonance cholangiopancreatography (MRCP) may be useful to detect bile duct stones. Endoscopic retrograde cholangiopancreatography (ERCP) is usually guided by fluoroscopy, however, endoscopic ultrasound has been used to guide removal of bile duct stones.
Cases of pancreatitis during pregnancy are more complex to manage and image. Ultrasound can diagnose some of the complications of pancreatitis such as fluid collection or pseudocysts. However, in rare cases where the maternal life is in danger, contrast-enhanced CT may be considered. MRI can be used to detect choledocholithiasis, if ultrasound is non-diagnostic. Without proper diagnostic information, pancreatitis and its complications may cause either maternal or fetal morbidity or mortality.
Urolithiasis is the most common etiology of non-traumatic pain in the pregnant patient that results in hospitalization. Seventy percent to 80% of ureteral calculi in pregnant patients pass spontaneously. However, renal obstruction can result in pyelonephritis or pyonephrosis and premature labor. Ultrasound is the first imaging procedure used to check not only for hydronephosis, but also for other etiologies that may cause abdominal pain (Table 9). Ultrasound is quite good for detecting hydronephrosis. However, it may be difficult to differentiate physiologic hydronephrosis of pregnancy and hydronephrosis secondary to a stone.
[TABLE 9 OMITTED]
[FIGURE 8 OMITTED]
[FIGURE 9 OMITTED]
Several imaging features are helpful to detect urolithiasis as the etiology of hydronephrosis (Table 10). These include observation of other renal stones as a secondary sign, as with the presence of a non-obstructing stone there is a higher risk of an obstructive calculi. On occasion, ultrasound can directly detect the obstructive calculus. Proximal stones in the uretero-pelvic junction may be detected while scanning the kidney (Figure 8). Distal stones may be detected through the bladder in early pregnacy. Endovaginal ultrasound may also be used to detect distal ureteral stones. Lack of ureteral jets within the bladder would indicate complete obstruction. Ultrasound may be used for guidance of interventional techniques such as percutaneous nephros- tomy or placement of a double "J" stent from the bladder into the renal pelvis. Shokeir et al. have used 2 measures to predict obstruction: a resistive index (RI) of 0.70, or an RI difference between the normal and abnormal kidney of 0.04. (12)
[FIGURE 10 OMITTED]
[FIGURE 11 OMITTED]
[FIGURE 12 OMITTED]
MR urography should be used as a secondary test when ultrasound fails to establish a diagnosis of hydronephrosis secondary to stone disease. MR urography in physiological hydrone-phrosis shows tapering in the mid portion, due to compression between the uterus and the psoas muscle. With stone disease, MR urography shows renal enlargement and edema, peri-renal fluid and the possibility of intraluminal filling defect (Figure 9).
If all else fails, then a non-contrast CT can be used. CT has a high sensitivity and specificity for the diagnosis of nephrolithiasis and ureterolithiasis. It has been shown in multiple studies that reasonable reductions in mA do not impair evaluation for urolithiasis and this should be employed for the pregnant patient (Figure 10).
There are a number of different etiologies of abdominal pain in pregnant patients that have not been addressed in this article. Some of those etiologies are considered in Tables 9 and 11 and demonstrated in Figures 11 and 12. Acute abdominal pain in the pregnant patient remains a diagnostic dilemma because of the multitude of factors addressed above. With a variety of imaging tools available, this review, and the included tables and figures, are intended to inform the clinical decision making regarding imaging options that are considerate of both patients: The mother and fetus.
(1.) Ralls PW, Balfe DM, Bree RL, et al. Evaluation of acute right lower quadrant pain. In: ACR appropriateness criteria. Reston, VA: American College of Radiology, 1999:1-8.
(2.) Rosenfield AT, Newhouse JH, Bluth EI, et al. Acute onset flank pain, suspicion of stone disease. In: ACR appropriateness criteria. Reston, VA: American College of Radiology, 1998:1-3.
(3.) Meadows M. Pregnancy and the drug dilemma. FDA Consum. 2001 ;35:16-20.
(4.) Jaffe TA, Miller CM, Merkle EM. Practice patterns in imaging of the pregnant patient with abdominal pain: A survey of academic centers. AJRAm J Roentgenol. 2007;189:1128-1134.
(5.) Thomton FJ, Paulson EK, Yoshizumi TT, et al. Single versus multi-detector row CT: Comparison of radiation doses and dose profiles. Acad Radiol. 2003;10:379-385.
(6.) Hurwitz LM, Yoshizumi T, Reiman RE, et al. Radiation dose to the fetus from body MDCT during early gestation. AJR Am J Roentgenol. 2006;186:871-876.
(7.) Patel SJ, Reede DL, Katz DS, et al. Imaging the pregnant patient for nonobstetric conditions: Algorithms and radiation dose considerations. Radiographics. 2007;27:1705-1722.
(8.) Richards JR, Ormsby EL, Romo MV, et al. Blunt abdominal injury in the pregnant patient: Detection with US. Radiology. 2004;233:463-470.
(9.) Barloon TJ, Brown BP, Abu-Yousef MM, et al. Sonography of acute appendicitis in pregnancy. Abdom Imaging. 1995;20:149-151.
(10.) Lim HK, Bae SH, Seo GS. Diagnosis of acute appendicitis in pregnant women: Value of sonography. AJRAm J Roentgenol. 1992;159:539-542.
(11.) Ginier B, McGahan JP. Percutaneous cholecystostomy for management of acute cholecystis in pregnancy. J Interv Radiol. 1992;7:87-89.
(12.) Shokeir AA, Mahran MR, Abdulmaaboud M. Renal colic in pregnant women: Role of renal resistive index. Urology. 2000;55:344-347.
John P. McGahan, MD, FACR, Ramit Lamba, MD, MBBS, and Fergus V. Coakley, MD
Dr. McGahan is Professor and Vice Chair, Department of Radiology, and Dr. Lamba is Assistant Professor, Department of Radiology, University of California, Davis Medical Center, Sacramento, CA; Dr. Coakley is a Professor of Radiology and Biomedical Imaging, and Urology, in the Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
Table 1. Protocol for MRI in Suspected Appendicitis in Pregnancy Seg Plane TRITE Flip/ET Localizer - - - SSFSE Coronal Infinity/100 100+ SSFSE Axial Infinity/100 100+ SSFSE Sagittal Infinity/100 100+ FRFSE (T1) Axial 500/7eff /4 FRFSE (T2) Axial 3100/90 /14 Seg BW FOV Slice/gap (kHz) (cm) (Frl/Ph) Localizer - - - SSFSE 62.5 32-40 6/1 SSFSE 62.5 32-40 6/1 SSFSE 62.5 32-40 6/1 FRFSE (T1) 62.5 32-40 6/1 FRFSE (T2) 62.5 32-40 6/1 Seg Matrix NEX Comment Localizer - - Center coil over mid abdomen SSFSE 256/160-192 .05 Overview/second localizer, include kidneys SSFSE 256/160-192 .05 Cover appendixin lower abdomen, do a second setif needed to cover upper half of the abdomen SSFSE 256/160-192 .05 Cover RLQ FRFSE (T1) 256/160 .05 Non FS T1, Scan is about 22 sec FRFSE (T2) 256/160 .05 FS T2 (similar to abdomen T2), if noise, use respiratory gating Table 2. European Society of Uroradiology (ESUR) Guidelines on the Use of Iodinated Gadolinium Contrast Media During Pregnancy and Lactation (Version 5.0 2006) Pregnancy Iodinated agents Gadolinium agents A. In exceptional circumstances, when radiographic examination is essential, iodinated contrast media may be given to the pregnant female. B Following administration of iodinated agents to the mother during pregnancy, thyroid function should be checked in the Lactation neonate during the first week. Pregnant or Breast feeding may be continued normally lactating mother when iodinated agents are given to the mother. with renal No additional precautions are necessary for the impairment fetus or neonate. Follow ESUR guidelines for contrast media administration when renal function is impaired. Pregnancy A. When MR examination is necessary, gadolinium media may be given to the pregnant female. B. Following administration of gadolinium agents to the mother during pregnancy, no neonatal tests are necessary. Lactation Breast feeding may be continued normally when gadolinium agents are given to the mother. Pregnant or No additional precautions are necessary for the lactating mother fetus or neonate. Follow ESUR guidelines for with renal contrast media administration when renal impairment function is impaired. Table 3. Administration of Iodinated Contrast to Pregnant Patients from the ACR Manual on Contrast Media Version 6.0 (summarized) Intravenously injected iodinated contrast media, has been shown to cross the human placenta and enter the fetus in measurable quantities. These agents get excreted via the urine into the amniotic fluid. Studies are limited and effects on the human embryo or fetus are unknown. A reasonable attempt should be made to identify pregnant patients prior to a CT exam and the use of iodinated contrast media. In a pregnant patient, both the potential radiation risk and the potential added risks of contrast media should be considered before proceeding with the study. While it is not possible to conclude that contrast agents present a definite risk to the fetus, there is insufficient evidence to conclude that they pose no risk. Consequently, the Committee recommends the following: A. The radiologist should confer with the referring physician and document in the radiology report or the patient's medical record the following: 1. That the information requested and necessity for contrast material administration cannot be acquired via other means (e.g., ultrasonography). 2. That the information needed affects the care of the patient and fetus during the pregnancy. 3. That the referring physician is of the opinion that it is not prudent to wait to obtain this information until after the patient is no longer pregnant. B. It is recommended that pregnant patients undergoing a diagnostic imaging examination with ionizing radiation and iodinated contrast material provide informed consent to document that they understand the risks/ benefits of the procedure to be performed and the alternative diagnostic options available to them (if any), and that they wish to proceed. Table 4. Causes of Acute Pain in Pregnancy--Partial List Trauma Renal Appendicitis Cholecystitis, hepatobiliary Hydronephrosis, pyelonephritis Pancreatitis Bowel obstruction Table 7. Ultrasound Findings for Acute Appendicitis * Non compression * Blind ending * Tubular structure >6 mm in diameter * Appendicolith * Mesenteric stranding * Free fluid Table 10. Ultrasound Findings Helpful to Predict Hydronephrosis Secondary to Ureteral Calculi * Marked discrepancy in hydronephrosis side to side * Demonstration of any renal stone (non-specific) * Lack of ureteral jet * Demonstration of ureteral stone * Elevated resistive index Table 11. Other Non-Obstetrical Causes of Abdominal Pain in Pregnant Patients * Intestinal obstruction -Large bowel -Small bowel * Hepatic rupture -HELLP syndrome (hemolysis, elevated liver enzymes, low platelet count) -Acute fatty liver -Hypertension -Intrahepatic cholestasis
|Printer friendly Cite/link Email Feedback|
|Author:||McGahan, John P.; Lamba, Ramit; Coakley, Fergus V.|
|Article Type:||Clinical report|
|Date:||Nov 1, 2010|
|Previous Article:||Cardiovascular magnetic resonance from basics to clinical applications.|
|Next Article:||Intraventricular cavernoma.|