BILE-DUCT STENTS - IS THERE AN INCREASED RATE OF COMPLICATIONS IN PATIENTS RECEIVING CHEMOTHERAPY

Citation
Fj. Lofts et al., BILE-DUCT STENTS - IS THERE AN INCREASED RATE OF COMPLICATIONS IN PATIENTS RECEIVING CHEMOTHERAPY, European journal of cancer, 33(2), 1997, pp. 209-213
Citations number
17
Categorie Soggetti
Oncology
Journal title
ISSN journal
09598049
Volume
33
Issue
2
Year of publication
1997
Pages
209 - 213
Database
ISI
SICI code
0959-8049(1997)33:2<209:BS-ITA>2.0.ZU;2-4
Abstract
The aim of this study was to determine whether palliative chemotherapy accelerates the rate of biliary stent occlusion, in patients with a m alignant biliary obstruction. Such treatment can induce neutropenia an d increase the risk of bacterial sepsis. Overgrowth of bacteria within the bile of patients receiving chemotherapy could accelerate the rate of stent occlusion. Retrospective analysis of treatment records for 8 0 consecutive patients with a diagnosis of adenocarcinoma arising from the pancreas, bile ducts or gall bladder was conducted. Two groups we re identified, those with a biliary stent in situ (primary stent group : 47/80; 59%) at the time of referral and those without (no stent grou p: 33/80; 41%). The majority of patients went on to receive chemothera py, 64% and 70% in the primary stent group and no stent group, respect ively. The rate of febrile neutropenia was similar in the two groups ( 5% versus 7% of all chemotherapy cycles in the primary stent group and no stent group, respectively). The rate of stent occlusion was not si gnificantly different between those exposed to chemotherapy (37%; 95% CI 20-54%) and those unexposed (39%; 95% CI 19-59%). Similarly, the me an duration of patency was not shortened by chemotherapy (105 days in the chemotherapy group versus 119 days in the non-chemotherapy group; P = 0.97, Mann-Whitney U-test). We conclude that there is no evidence of increased rate of bile duct-related complications in patients recei ving chemotherapy. In particular, we find no indication for the use of prophylactic antibiotics. (C) 1997 Elsevier Science Ltd.