Abstract
Purpose
Physiologic uptake of 2-[18F]-fluoro-2-deoxy-d-glucose (FDG) by bowel can confound positron emission tomography/computed tomography (PET/CT) assessment for abdominal pathology, particularly within the bowel itself. We wished to determine if oral administration of the antimotility agent, Lomotil (5 mg diphenoxylate hydrochloride/0.05 mg atropine sulfate; G.D. Searle and Company, a division of Pfizer), prior to PET/CT scanning would reduce physiologic uptake of FDG by the small bowel and colon (lower gastrointestinal [GI] tract).
Procedures
Patients undergoing PET/CT scans for lymphoma were enrolled in a prospective, randomized, double-blinded study and received either 10 mL water (control group) or 10 mL Lomotil (experimental group) orally 30–60 min prior to scanning. Scans were reviewed independently by two blinded experienced readers and scored for the degree of FDG activity in the lower GI tract relative to liver activity.
Results
The administration of Lomotil prior to PET/CT scanning did not reduce physiologic FDG activity in the small bowel and colon. In contrast, increased radiotracer uptake by the lower GI tract was observed in the Lomotil group compared to the control group.
Conclusions
Pretreatment with Lomotil prior to PET/CT scanning confers no benefit toward the reduction of physiologic FDG uptake by the small bowel and colon.
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References
Spieth ME, Kasner DL (2002) A tabulated summary of the FDG PET literature. J Nucl Med 43(3):441
Juweid ME, Cheson BD (2006) Positron-emission tomography and assessment of cancer therapy. N Engl J Med 354(5):496–507
Rohren EM, Turkington TG, Coleman RE (2004) Clinical applications of PET in oncology. Radiology 231(2):305–332
Bogsrud TV, Lowe VJ (2006) Normal variants and pitfalls in whole-body PET imaging with 18F FDG. Appl Radiol 35(6):16–30
Sureshbabu W, Mawlawi O (2005) PET/CT imaging artifacts. J Nucl Med Technol 33(3):156–161, (quiz 163–164)
Ghassan E-H et al (2004) Normal variants in [18F]-fluorodeoxyglucose PET imaging. Radiol Clin North Am 42:1063–1081
Kostakoglu L et al (2004) PET-CT fusion imaging in differentiating physiologic from pathologic FDG uptake. Radiographics 24(5):1411–1431
Shreve PD, Anzai Y, Wahl RL (1999) Pitfalls in oncologic diagnosis with FDG PET imaging: physiologic and benign variants. Radiographics 19(1):61–77, (quiz 150–151)
von Schulthess GK, Steinert HC, Hany TF (2006) Integrated PET/CT: current applications and future directions. Radiology 238(2):405–422
de Groot M et al (2005) Influence of blood glucose level, age and fasting period on non-pathological FDG uptake in heart and gut. Eur J Nucl Med Mol Imaging 32(1):98–101
Zhuang H et al (2002) Incidental detection of colon cancer by FDG positron emission tomography in patients examined for pulmonary nodules. Clin Nucl Med 27(9):628–632
Kim S et al (1999) Relationship between gastrointestinal F-18-fluorodeoxyglucose accumulation and gastrointestinal symptoms in whole-body PET. Clin Positron Imaging 2(5):273–279
Kamel EM et al (2004) Significance of incidental 18F-FDG accumulations in the gastrointestinal tract in PET/CT: correlation with endoscopic and histopathologic results. J Nucl Med 45(11):1804–1810
Pandit-Taskar N et al (2004) Clinical significance of unexplained abnormal focal FDG uptake in the abdomen during whole-body PET. AJR Am J Roentgenol 183(4):1143–1147
Tatlidil R et al (2002) Incidental colonic fluorodeoxyglucose uptake: correlation with colonoscopic and histopathologic findings. Radiology 224(3):783–787
Yasuda S et al (2001) 18F-FDG PET detection of colonic adenomas. J Nucl Med 42(7):989–992
Stahl A et al (2000) Effect of N-butylscopolamine on intestinal uptake of fluorine-18-fluorodeoxyglucose in PET imaging of the abdomen. Nuklearmedizin 39(8):241–245
SAS Institute (1999) SAS OnlineDoc®. SAS Institute, Cary, NC
Freeman GH, Halton JH (1951) Note on an exact treatment of contingency, goodness of fit and other problems of significance. Biometrika 38(1–2):141–149
Hannah A et al (1996) Abnormal colonic accumulation of fluorine-18-FDG in pseudomembranous colitis. J Nucl Med 37(10):1683–1685
Steadman CJ et al (1992) Control of muscle tone in the human colon. Gut 33(4):541–546
Jadvar H, Schambye RB, Segall GM (1999) Effect of atropine and sincalide on the intestinal uptake of F-18 fluorodeoxyglucose. Clin Nucl Med 24(12):965–967
DRUGDEX. Diphenoxylate hydrochloride/atropine sulfate. In: DRUGDEX® system (internet database). Periodic (cited 2008)
Karim A et al (1972) Pharmacokinetics and metabolism of diphenoxylate in man. Clin Pharmacol Ther 13(3):407–419
Acknowledgments
We would like to thank our study coordinator, Terry L. Brinkman, for her extensive assistance. Statistical services were provided by W.S. Harmsen and R.A. Meverden in the Division of Biostatistics. This work was supported by the Mayo Foundation.
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Murphy, R., Doerger, K.M., Nathan, M.A. et al. Pretreatment with Diphenoxylate Hydrochloride/Atropine Sulfate (Lomotil) does not Decrease Physiologic Bowel FDG Activity on PET/CT Scans of the Abdomen and Pelvis. Mol Imaging Biol 11, 114–117 (2009). https://doi.org/10.1007/s11307-008-0178-8
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DOI: https://doi.org/10.1007/s11307-008-0178-8