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Evaluation of Results of the Prostigmine-morphine Test with Quantitative Hepatobiliary Scintigraphy: a New Method for the Diagnosis of Sphincter of Oddi Dyskinesia

Overview
Journal Eur J Nucl Med
Specialty Nuclear Medicine
Date 1995 Mar 1
PMID 7789395
Citations 6
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Abstract

Attempts have long been made to use the prostigmine-morphine provocation test for the selection of postcholecystectomy patients suffering from sphincter of Oddi (SO) dyskinesia. Since the whole procedure is based upon the evaluation of subjective complaints, this test has frequently been criticized. To improve the diagnostic value of this method, we have visualized SO spasms during prostigmine-morphine provocation by means of quantitative hepatobiliary scintigraphy (QHBS). Twenty-two cholecystectomized patients with typical postprandial biliary pain were included in this study. In the first series of studies, QHBS with technetium-99m 2,6-diethylphenylcarbamoylmethyl-diacetic acid was performed in each patient 2 days before prostigmine-morphine provocation. The time to peak activity (Tmax) and the half-time of excretion (T1/2) over the liver parenchyma (LP), hepatic hilum (HH) and common bile duct (CBD), and the duodenum appearance time (DAT), were determined and served as control values. In the second series of experiments, sphincter spasms were evoked by prostigmine-morphine administration and visualized by means of QHBS. The same parameters were evaluated and serum levels of aspartate aminotransferase (AST) were determined simultaneously at regular intervals. In 12 patients who responded to prostigmine-morphine provocation with typical biliary pain and a significant AST elevation (Nardi positive group) the hepatobiliary scintigram demonstrated a marked biliary obstruction. Tmax and T1/2 over the LP, HH and CBD were significantly increased, while DAT was significantly longer relative to the corresponding data obtained without provocation. Four of the remaining ten patients indicated atypical abdominal pain during prostigmine-morphine provocation, but the AST level remained unchanged in all ten (Nardi negative group).(ABSTRACT TRUNCATED AT 250 WORDS)

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References
1.
Schmalz M, GEENEN J, Hogan W, Dodds W, Venu R, Johnson G . Pain on common bile duct injection during ERCP: does it indicate sphincter of Oddi dysfunction?. Gastrointest Endosc. 1990; 36(5):458-61. DOI: 10.1016/s0016-5107(90)71114-5. View

2.
Varro V, Dobronte Z, Hajnal F, Csernay L, Nemessanyi Z, LANG J . The diagnosis of hypertonic Oddi's sphincter dyskinesia. Am J Gastroenterol. 1983; 78(11):736-9. View

3.
Toouli J . What is sphincter of Oddi dysfunction?. Gut. 1989; 30(6):753-61. PMC: 1434151. DOI: 10.1136/gut.30.6.753. View

4.
Guelrud M . Papillary stenosis. Endoscopy. 1988; 20 Suppl 1:193-202. DOI: 10.1055/s-2007-1018175. View

5.
GEENEN J, Hogan W, Dodds W, STEWART E, Arndorfer R . Intraluminal pressure recording from the human sphincter of Oddi. Gastroenterology. 1980; 78(2):317-24. View