Endosc Int Open 2016; 04(10): E1096-E1100
DOI: 10.1055/s-0042-114982
Original article
© Georg Thieme Verlag KG Stuttgart · New York

Endoscopic sphincterotomy and risk of cholangiocarcinoma: a population-based cohort study in Finland and Sweden

Cecilia Strömberg
1   Division of Surgery, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden
2   Centre for Digestive Diseases, Karolinska University Hospital, Stockholm, Sweden
,
Camilla Böckelman
3   Department of Surgery, Vaasa Central Hospital, Vaasa, Finland
,
Huan Song
4   Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden
,
Weimin Ye
4   Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden
,
Eero Pukkala
5   Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland
6   School of Health Sciences, University of Tampere, Tampere, Finland
,
Caj Haglund
7   Department of Surgery, University of Helsinki and Helsinki University Hospital, Finland
,
Magnus Nilsson
1   Division of Surgery, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden
2   Centre for Digestive Diseases, Karolinska University Hospital, Stockholm, Sweden
› Author Affiliations
Further Information

Publication History

submitted30 March 2016

accepted after revision29 July 2016

Publication Date:
14 September 2016 (online)

Background and study aims: Elevated long-term risk of cholangiocarcinoma is reported after endoscopic sphincterotomy (ES), but in a previous study we found a trend towards a decreased risk. The aim of this study was to evaluate the association in a larger cohort with a longer follow-up.

Patients and methods: Data concerning all patients having had an inpatient endoscopic retrograde cholangiopancreatography (ERCP) were collected from the hospital discharge registries of Finland and Sweden. Incident cases of malignancy were identified through linkage to the nationwide Cancer Registries. Patients with a diagnosis of malignancy, before or within 2 years of the ERCP, were excluded. The cohorts were followed until a diagnosis of malignancy, death or emigration, or end of follow-up (end of 2010). The relative risk of malignancy was calculated as standardized incidence ratio (SIR) compared with the general population, inherently adjusting for age, gender, and calendar year of follow-up.

Results: A total of 69 925 patients undergoing ERCP from 1976 through 2008 were included in the pooled cohort. ES was performed in 40 193 subjects. The risk of malignancy was elevated in the total cohort (SIR = 2.3; 95 % confidence interval [CI] 2.1 – 2.5) irrespective of whether ES was performed or not. The SIRs diminished with duration of follow-up.

Conclusions: We found an elevated risk of malignancy both in the bile ducts alone and in the bile ducts, liver or pancreas together, after ERCP. The risk was the same, regardless of whether ES had been performed or not, so ES was unlikely to be the cause, and a common carcinogenic exposure previous to the ERCP procedure, possibly ductal gallstone disease, was more likely.

 
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