Abstract
Background
The risk of gallstone disease necessitating cholecystectomy after ileal resection (IR) in Crohn’s disease (CD) patients is not well established. We studied the incidence, cumulative and relative risk of cholecystectomy after IR in CD patients, and associated risk factors.
Methods
CD patients with a first IR between 1991 and 2015 were identified in PALGA, a nationwide pathology database in the Netherlands. Details on subsequent cholecystectomy and IR were recorded. Yearly cholecystectomy rates from the general Dutch population were used as a reference.
Results
A cohort of 8302 (3466 (41.7%) males) CD patients after IR was identified. During the 11.9 (IQR 6.3–18.0) years median follow-up, the post-IR incidence rate of cholecystectomy was 5.2 (95% CI 3.5–6.4)/1000 persons/year. The cumulative incidence was 0.5% at 1 year, 2.4% at 5 years, 4.6% at 10 years, and 10.3% after 20 years. In multivariable analyses, female sex (HR 1.9, CI 1.5–2.3), a later calendar year of first IR (HR/5-year increase, HR 1.27, CI 1.18–1.35), and ileal re-resection (time-dependent HR 1.37, CI 1.06–1.77) were associated with cholecystectomy. In the last decade, cholecystectomy rates increased and were higher in our postoperative CD population than in the general population (relative incidence ratio 3.13 (CI 2.29–4.28; p < 0.0001) in 2015).
Conclusions
Although higher in females, increasing in recent years, and higher than in the general population, the overall risk of cholecystectomy in CD patients following IR is low and routine prophylactic measures seem unwarranted.
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Introduction
The annual incidence of newly diagnosed gallstones in Crohn’s disease (CD) patients is twice as high as compared to the general population.1 Ileal disease localization and previous ileal resection (IR) have both been identified as risk factors for developing gallstones in CD patients.1,2 The underlying pathophysiology for the increased risk of developing gallstones in CD patients with ileal disease or after IR is not fully understood. A disturbance of the enterohepatic cycle of bilirubin, due to bile salt malabsorption in the ileum, may increase bilirubin secretion into the bile and thereby increase formation of gallstones. Alternative hypotheses are supersaturation of cholesterol in the bile due to reduced bile salt absorption or reduced motility and emptying of the gallbladder.3,4,5,6,7
Data on the prevalence of gallstones diagnosed with abdominal ultrasound in CD patients are variable, probably due to the inclusion of pooled populations of both symptomatic and asymptomatic CD patients. The reported prevalence ranges from respectively 10.4 to 38.5% in females and 9.4 to 25% in males and is clearly higher as compared to the reported prevalence in the asymptomatic general population, respectively 10.5% in females and 6.5% in males.1,2,6,8,9,10 Available epidemiological data suggests an increased risk of symptomatic and/or complicated gallstone disease in CD patients.1,2,6,10 A case-control study in 429 CD patients showed that the incidence rate of gallstones on abdominal ultrasound was 14.35/1000 persons/year compared to 7.48/1000 persons/year in matched hospital controls.1 Additionally, this study suggested a significant proportion of patients with newly diagnosed gallstones would eventually require cholecystectomy for symptomatic gallstone disease ([9/41] 22%). A major limitation of this and other reports is the inclusion of small CD populations and lack of long-term follow-up data. In order to interpret the clinical relevance of the observed increased risk of gallstones in CD patients, studies assessing the risk of gallstone disease necessitating cholecystectomy are necessary. A high risk of cholecystectomy after IR justifies increased alertness in symptomatic CD patients and possibly even prophylactic measures at the time of IR, such as synchronous cholecystectomy. In this nationwide long-term follow-up study in the Netherlands, we aimed to assess the risk of—and identify risk factors for—cholecystectomy during long-term follow-up after IR in CD patients, including absolute annual and cumulative risk as well as the relative risk as compared to the general population.
Materials and Methods
Histopathology Database
In the Netherlands, all histopathology and cytopathology reports are collected in the nationwide network and registry of histopathology and cytopathology in the Netherlands (PALGA). Since 1991, this database has a nationwide coverage.11 Every individual patient within the database is identified with a unique code that allows follow-up of all consequent pathology reports, regardless of the institute the patient is being treated. Every record in the database contains an excerpt combined with diagnostic codes given by the pathologist who assessed the tissue. The codes used are similar to the Systematized Nomenclature of Medicine (SNOMED) classification of the College of American Pathologists.12 After a report has been coded, it is submitted online to the central database. The current study was based on data recorded in the PALGA database between 1991 and 2015. For each patient, the following characteristics were available: gender, date of birth, date of pathology review, summary text, and diagnostic code.
Patient Selection
All patients aged ≥ 18 years with an IR (ileal or ileocolonic resection) and simultaneous histological diagnosis CD in the period from 1991 to 2015 were identified in PALGA. Corresponding details on subsequent IR and cholecystectomy were identified using PALGA pathology codes (Appendix). Patients with a diagnosis of malignancy in the initial bowel resection specimen were excluded. Duplicate pathology reports (e.g., revision material) were excluded. Furthermore, patients with cholecystectomy prior to IR and patients of whom the first available excerpt in our database was an ileal re-resection were excluded. Patients with a cholecystectomy with gallbladder carcinoma, or gallbladder specimens resected in combination with other procedures such as hepatectomy or Whipple procedure, were excluded form analysis. Follow-up data were evaluated until December 2015. In addition, we obtained the yearly cholecystectomy rates for the general Dutch population aged ≥ 18 years from 1991 to 2015, using PALGA pathology codes, to create a reference study population (Appendix).
Statistical Analysis
Statistical analyses were performed with IBM SPS Statistics version 22.0 (IBM Corp. Released 2013, IBM Corp, Armon, NY) and R version 3.4.0 (2017-4-21, R Foundation for Statistical Computing, Vienna, Austria) with the packages survival and splines.13,14 Data are presented as median and interquartile range (IQR) for continuous variables. The PALGA database does not contain follow-up data on date of death unless an autopsy has been performed. Therefore, censoring for patient death was imputed from survival data of the general Dutch population from the Statistics Netherlands agency (CBS).15 For each patient, the imputed follow-up was based on life expectancy in his or her year of birth, assuming the survival of CD patients is similar to that of the general population.16,17 Interval between IR and cholecystectomy and cumulative incidence of cholecystectomies was evaluated using Kaplan-Meier survival analysis. Univariate and multivariate Cox-regression analysis was performed to identify factors associated with cholecystectomy.
The association of a second IR with a subsequent cholecystectomy was assessed by modeling the time until a second IR as a time-dependent covariate. Accompanying Kaplan-Meier estimations were made using a clock-reset approach.18 In this figure, a cumulative incidence curve was plotted for patients who only had one IR. Those who had a second resection during follow-up were censored and switched to a new cumulative incidence curve starting at time 0.
In addition, we assessed the yearly crude incidence rates of cholecystectomy in our CD population as well as in the general Dutch population. Cholecystectomy rates of the general Dutch population were obtained from PALGA. Data on total population numbers over calendar years were obtained from a Dutch registry (Statistics Netherlands, www.cbs.nl).19 Joinpoint Regression Program, version 4.5.0.1, was used to examine significant changes in incidence over calendar time between 1991 and 2015.20 Relative incidence ratios (relative risk) of cholecystectomy between our CD cohort and the general Dutch population were calculated at yearly intervals for the period 2001–2015 according to Altman.21
This study was conducted in accordance with the protocol and the principles of the Declaration of Helsinki. The protocol was approved by the Institutional Research Board of the corresponding center.
Results
Baseline Cohort Characteristics
A cohort of 8506 adult CD patients who underwent an ileal resection between 1991 and 2015 was retrieved. After applying exclusion criteria, 8302 patients were included for further analysis (Fig. 1). The majority of patients was female (4836; 58.3%) and the median (IQR) age at the first resection was 37.0 (27.0–51.0) years (Table 1). Median follow-up was 11.98 (IQR 6.31–18.05; range 0.0–25.0) years.
Cumulative Incidence of Cholecystectomy
At the end of the 25-year follow-up period, a total of 523 (6.3%) patients had undergone a cholecystectomy: 143 males (1.7% of total population and 4.5% of male study population) and 380 females (4.6% of total population and 7.9% of female study population). The median (IQR) age at cholecystectomy was 45.65 (37.36–56.62) years. The incidence rates of cholecystectomy at 1, 5, 10, and 20 years of follow-up were 0.5%, 2.4%, 4.6%, and 10.3%, respectively (Fig. 2). Female CD patients had higher incidence rates of cholecystectomy than male patients: 0.6% vs. 0.3%, 2.8% vs. 1.9%, 5.7% vs. 3.1%, and 12.7% vs. 6.7%, at 1, 5, 10, and 20 years, respectively (Fig. 2).
Factors Associated with Cholecystectomy
In univariable analysis, female patients had a significantly higher probability of cholecystectomy than male patients (HR 1.84 (95% confidence interval [CI] 1.52–2.23); p < 0.001; Fig. 2). Furthermore, a later calendar year of the first IR was associated with an increased probability of cholecystectomy (HR/5-year increase 1.25; CI 1.16–1.34; Fig. 3). Finally, ileal re-resection during follow-up was associated with a slightly increased probability of cholecystectomy (time-dependent HR 1.30; CI 1.01–1.68; p = 0.045; Fig. 4). All these variables remained significantly associated with a cholecystectomy in multivariable analysis (Table 2).
Yearly Cholecystectomy Rates in CD Patients and the General Population
During the median follow-up of 12 years, the incidence rate of cholecystectomy in our CD cohort was 5.2 (95% CI 3.5–6.4)/1000 persons/year. Females had a significantly higher rate than males (6.4 [95% CI 4.7–5.6] vs. 3.5 [95% CI 2.9–4.1]/1000 persons/year; p < 0.0001). Absolute cholecystectomy rates per calendar year were higher in our postoperative CD population (Fig. 5a) than in the general Dutch population (Fig. 5b) between 1991 and 2015. Over the last decade, the relative incidence ratio for our postoperative CD cohort, compared to the general population, varied between 1.28 (95% CI 1.28–2.81; p = 0.001) in 2002 and 3.13 (95% CI 2.29–4.28; p < 0.0001) in 2015. For males, these ratios were 2.16 (95% CI 1.028–4.52; p = 0.042) and 3.25 (95% CI 1.85–5.72; p < 0.0001) and for females 1.68 (95% CI 1.06–2.67; p = 0.027) and 2.90 (1.99–4.22; p < 0.0001), respectively (Supplementary table 1). In accordance with the observed increase in the probability of cholecystectomy after IR in our CD population over calendar time, there was an increase in the crude incidence rates of cholecystectomies within the study population (Fig. 5a), which was also observed in the general Dutch population with a significant increase over calendar time from 48/100,000 in 1991 to 185/100,000 in 2006, and remained relatively stable with a minimal decline after 2012 (Fig. 5b).
Discussion
It has been well established that CD patients are at an increased risk of gallstone development, especially those with ileal involvement. The clinical relevance of this observed increase has however remained unclear. This large nationwide long-term follow-up study is the first to assess the risk of gallstone disease necessitating an intervention following IR, namely cholecystectomy. Our results show that, although over the past years the incidence of cholecystectomy in post-IR CD patients has increased and is currently higher than that in the general population, the annual incidence of cholecystectomy after IR is low. With thorough analyses, we were able to identify patients more likely to require cholecystectomy following IR. Female patients, those undergoing ileal re-resection, and patients with a later calendar year of first IR have an increased probability of cholecystectomy.
The observed incidence rate of cholecystectomy in our CD population after IR of 5.2/1000 persons/year is evidently lower than the reported incidence rate of gallstones found by ultrasound examination in CD patients in general. A large case-control study in 429 CD patients reported an incidence rate of gallstones on abdominal ultrasound of 14.35/1000 persons/year, which was significantly higher than that in matched controls (7.75/1000 persons/year, p = 0.012).1 Additionally, it was shown that in a subgroup of CD patients with newly developed gallstones, about 22% of the patients (9/41) eventually required cholecystectomy for symptomatic stones. Our nationwide study substantially adds to these data by describing the clinical consequences of gallstones in a large long-term follow-up cohort of CD patients. Our study shows that in a potentially high-risk population for gallstone disease, only a minority of patients of approximately 10.5% during 20 years will eventually require a cholecystectomy.
The observed cumulative incidence of cholecystectomy of 4.6% within 15 years of follow-up in our study is evidently higher than that observed in the general population. A recent large population-based cohort study of over 65,000 individuals found a cumulative incidence of cholecystectomy for gallstone disease of 1.8% within 15 years of follow-up.22 To date, the only published study on gallstone disease necessitating cholecystectomy in CD patients was a case-control study including 134 CD patients with ileitis.10 This study demonstrated that the incidence of cholecystectomy was not significantly different from an age- and sex-matched control group. The nationwide data in the current study significantly adds to previous reports by quantifying the rate of cholecystectomy in absolute and relative risk, annual cholecystectomy risk, and cumulative cholecystectomy risk during long-term follow-up.
Female sex is an important risk factor for cholecystectomy after IR in our study. This finding is in agreement with data from the general population, in which female sex has been identified as an important risk factor for gallstone development.9,23 Especially women in fertile years are more likely to form gallstones as compared to men. This difference narrows after menopause.24,25 However, previous data on the prevalence of gallstones in CD patients indicate there are no gender differences. A study in 251 CD patients showed no gender differences in the prevalence of gallstones (27% in females vs. 29% in males).2 In accord, a more recent study in 330 CD patients reported similar results with a prevalence of 25% in females vs. 25% in males as found by ultrasound examination.6 A possible explanation for the observed difference in our cohort may be the long-term follow-up and the larger number of included CD patients. Alternatively, the difference may be explained by our cohort’s relatively young median age of 37 years.
In line with expectations, ileal re-resection was associated with cholecystectomy. Previous studies have shown that the prevalence of gallstones is associated with the number of bowel resections and is significantly increased in patients in whom more than 10 cm of the ileum was resected.2,26 In the current study, we assessed re-resection as a surrogate for the length of intestine removed by surgery and/or CD severity, and this was associated with an increased risk of cholecystectomy.
To our knowledge, this is the first study to report on an increase in gallstone disease necessitating cholecystectomy after IR in CD patients over calendar time. Our findings may well reflect the global trend of increasing gallstone prevalence observed in necroptic27 and ultrasound studies.24,28 In addition, cholecystectomy rates have increased, especially in the first decade after 1990.29,30,31 This increase may be attributed to the introduction of laparoscopic cholecystectomy in 1990, which may have lowered the threshold for a surgical procedure in cases of uncomplicated gallstones.32,33 Still, the cholecystectomy rates may vary greatly between different countries. A recent nationwide study from Sweden, which assessed a total of 130,800 laparoscopic and 47,641 open cholecystectomies performed between 1998 and 2013, showed the annual rates of cholecystectomies remained stable.34 In contrast, our data covering all cholecystectomies performed within the Netherlands between 1991 and 2015 indicates annual rates have increased between 1991 and 2007 and remained relatively stable with a minimal decline after 2012. This corresponds with the observed increase in probability of cholecystectomy after IR in our study population.
One of the strengths of our study is the selection of a large nationwide cohort with long-term follow-up data, with stringent inclusion criteria of a histology-proven CD and the use of the general Dutch population as a reference population. These data allowed a thorough assessment of gallstone disease necessitating cholecystectomy including risk factors, absolute, relative, and cumulative risk. In addition, due to the nationwide coverage of PALGA, there was a long-term follow-up for each individual patient after IR and full-scale cholecystectomy detection. However, some limitations need to be considered. Firstly, our inclusion criteria for a biopsy-proven CD (SNOMED D62160) might have been too stringent as some pathology reports only include SNOMED codes for ulcer, granuloma, or inflammation. Secondly, the PALGA database provides limited data on patient characteristics, making further subgroup analysis impossible. No data on initial diagnosis of CD and thus duration and/or severity of disease, length of the resected segment, ileal involvement earlier in the disease course, or other known risk factors (e.g., BMI, bariatric surgery) are provided. It would be highly interesting to assess these factors in such a large cohort. In addition, the PALGA database does not contain a date of CD diagnosis, thereby limiting the possibilities for time-to-event and risk factor analysis in a cohort of CD patients without IR. Further studies could focus on the comparison of the risk of cholecystectomy in CD patients without IR and those with IR. This would provide further evidence for the hypothesized role of IR in the development of gallstones in CD patients. Finally, data on the indication of cholecystectomy are lacking. Cholecystectomy rates in CD patients might be higher due to frequent contact with health care professionals and consequently a lower threshold for performing an abdominal ultrasound and a higher diagnosis rate of incidental gallstones. Furthermore, cholecystectomy may have been performed for indications other than complications of chole(cysto)lithiasis, e.g., polyp, tumor-like lesions, acalculous cholecystitis, and unexplained abdominal pain. However, in general, only a small proportion of patients undergo cholecystectomy for these indications.34
In conclusion, this large nationwide study shows that annual incidence of cholecystectomy in CD patients after IR is 0.5% and increases almost linearly during follow-up to 10.5% after 20 years. Female sex, re-resection, and a later year of IR are associated with cholecystectomy. The incidence of cholecystectomy after IR in CD patients is currently three times higher than that in the general population. Nonetheless, overall, the risk of cholecystectomy is low. While this risk may justify increased alertness of gallstone disease and a lower threshold for abdominal ultrasound in symptomatic CD patients following ileal resection, it does not seem to warrant prophylactic synchronous cholecystectomy during IR in all CD patients.
Abbreviations
- CD:
-
Crohn’s disease
- IR:
-
Ileal resection
- HR:
-
Hazard ratio
- RR:
-
Relative incidence ratio
- CI:
-
Confidence interval
References
Parente F, Pastore L, Bargiggia S, Cucino C, Greco S, Molteni M, Ardizzone S, et al. Incidence and risk factors for gallstones in patients with inflammatory bowel disease: A large case-control study. Hepatology 2007;45:1267–1274.
Fraquelli M, Losco A, Visentin S, Cesana BM, Pometta R, Colli A, Conte D. Gallstone disease and related risk factors in patients with Crohn disease: analysis of 330 consecutive cases. Arch Intern Med 2001;161:2201–2204.
Lapidus A, Akerlund JE, Einarsson C. Gallbladder bile composition in patients with Crohn’s disease. World J Gastroenterol 2006;12:70–74.
Brink MA, Slors JFM, Keulemans YCA, Mok KS, De Waart DR, Carey MC, Groen AK, et al. Enterohepatic cycling of bilirubin: A putative mechanism for pigment gallstone formation in ileal Crohn’s disease. Gastroenterology 1999;116:1420–1427.
Pereira SP, Bain IM, Kumar D, Dowling RH. Bile composition in inflammatory bowel disease: ileal disease and colectomy, but not colitis, induce lithogenic bile. Aliment Pharmacol Ther 2003;17:923–933.
Hutchinson R, Tyrrell PN, Kumar D, Dunn JA, Li JK, Allan RN. Pathogenesis of gall stones in Crohn’s disease: an alternative explanation. Gut 1994;35:94–97.
Vu MK, Gielkens HA, van Hogezand RA, van Oostayen JA, Lamers CB, Masclee AA. Gallbladder motility in Crohn disease: influence of disease localization and bowel resection. Scand J Gastroenterol 2000;35:1157–1162.
Lapidus A, Bangstad M, Astrom M, Muhrbeck O. The prevalence of gallstone disease in a defined cohort of patients with Crohn’s disease. Am J Gastroenterol 1999;94:1261–1266.
Attili AF, Carulli N, Roda E, Barbara B, Capocaccia L, Menotti A, Okoliksanyi L, et al. Epidemiology of gallstone disease in Italy: prevalence data of the Multicenter Italian Study on Cholelithiasis (M.I.COL.). Am J Epidemiol 1995;141:158–165.
Chew SS, Ngo TQ, Douglas PR, Newstead GL, Selby W, Solomon MJ. Cholecystectomy in patients with Crohn’s ileitis. Dis Colon Rectum 2003;46:1484–1488.
Casparie M, Tiebosch AT, Burger G, Blauwgeers H, van de Pol A, van Krieken JH, Meijer GA. Pathology databanking and biobanking in The Netherlands, a central role for PALGA, the nationwide histopathology and cytopathology data network and archive. Cell Oncol 2007;29:19–24.
Cote RA, Robboy S. Progress in medical information management. Systematized nomenclature of medicine (SNOMED). Jama 1980;243:756–762.
Team. RC. R Foundation for Statistical Computing, Vienna, Austria, 2017a. URL https://www.R-project.org/. R: A Language and Environment for Statistical Computing.
Therneau. TM. A Package for Survival Analysis in S. URL https://CRAN.R-project.org/package=survival. version 2.38. 2015.
Gezonde levensverwachting; vanaf 1981 In: Centraal Bureau voor de Statistiek (CBS); 2015.
Hovde O, Kempski-Monstad I, Smastuen MC, Solberg IC, Henriksen M, Jahnsen J, Stray N, et al. Mortality and causes of death in Crohn’s disease: results from 20 years of follow-up in the IBSEN study. Gut 2014;63:771–775.
van den Heuvel TRA, Jeuring SFG, Zeegers MP, van Dongen DHE, Wolters A, Masclee AAM, Hameeteman WH, et al. A 20 year temporal change analysis in incidence, presenting phenotype and mortality in the Dutch IBDSL cohort - Can diagnostic factors explain the increase in IBD incidence? J Crohns Colitis 2017.
Putter H, Fiocco M, Geskus RB. Tutorial in biostatistics: competing risks and multi-state models. Stat Med 2007;26:2389–2430.
Bevolking kerncijfers, gezonde levensverwachting, vanaf 1991. In: Statline; Centraal Bureau voor de Statistiek; 2017.
Kim HJ, Fay MP, Feuer EJ, Midthune DN. Permutation tests for joinpoint regression with applications to cancer rates. Stat Med 2000;19:335–351.
Altman DG. Practical Statistics for Medical Research. London: Chapman and Hall. , 1991.
Talseth A, Ness-Jensen E, Edna TH, Hveem K. Risk factors for requiring cholecystectomy for gallstone disease in a prospective population-based cohort study. Br J Surg 2016.
Everhart JE, Khare M, Hill M, Maurer KR. Prevalence and ethnic differences in gallbladder disease in the United States. Gastroenterology 1999;117:632–639.
Stinton LM, Shaffer EA. Epidemiology of gallbladder disease: cholelithiasis and cancer. Gut Liver 2012;6:172–187.
Shaffer EA. Gallstone disease: Epidemiology of gallbladder stone disease. Best Pract Res Clin Gastroenterol 2006;20:981–996.
Hill GL, Mair WS, Goligher JC. Gallstones after ileostomy and ileal resection. Gut 1975;16:932–936.
Acalovschi M, Dumitrascu D, Caluser I, Ban A. Comparative prevalence of gallstone disease at 100-year interval in a large Romanian town, a necropsy study. Dig Dis Sci 1987;32:354–357.
Aerts R, Penninckx F. The burden of gallstone disease in Europe. Aliment Pharmacol Ther 2003;18 Suppl 3:49–53.
Lam CM, Murray FE, Cuschieri A. Increased cholecystectomy rate after the introduction of laparoscopic cholecystectomy in Scotland. Gut 1996;38:282–284.
McMahon AJ, Fischbacher CM, Frame SH, MacLeod MC. Impact of laparoscopic cholecystectomy: a population-based study. Lancet 2000;356:1632–1637.
Attili AF, De Santis A, Capri R, Repice AM, Maselli S. The natural history of gallstones: the GREPCO experience. The GREPCO Group. Hepatology 1995;21:655–660.
Steinle EW, VanderMolen RL, Silbergleit A, Cohen MM. Impact of laparoscopic cholecystectomy on indications for surgical treatment of gallstones. Surg Endosc 1997;11:933–935.
Mallon P, White J, McMenamin M, Das N, Hughes D, Gilliland R. Increased cholecystectomy rate in the laparoscopic era: a study of the potential causative factors. Surg Endosc 2006;20:883–886.
Noel R, Arnelo U, Enochsson L, Lundell L, Nilsson M, Sandblom G. Regional variations in cholecystectomy rates in Sweden: impact on complications of gallstone disease. Scand J Gastroenterol 2016;51:465–471.
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Authors and Affiliations
Contributions
Jorn C. Goet: Acquisition of data, analysis and interpretation of data, statistical analysis, drafting the manuscript
Evelien M. J. Beelen: Acquisition of data, analysis and interpretation of data, statistical analysis, drafting the manuscript
Katharina E. Biermann: Analysis and interpretation of data
Annette H. Gijsbers: Acquisition of data
W. Rudolph Schouten: Analysis and interpretation of data
C. Janneke van der Woude: Study concept and design, analysis and interpretation of data
Annemarie C. de Vries: Study concept and design, acquisition of data, analysis and interpretation of data
All authors critically revised the manuscript, and approved its final version to be published. All authors agree to be held accountable for all aspects of the work.
Corresponding author
Ethics declarations
This study was conducted in accordance with the protocol and the principles of the Declaration of Helsinki. The protocol was approved by the Institutional Research Board of the corresponding center.
Conflict of Interest
The authors declare that they have no conflict of interest.
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Appendix
Appendix
PALGA diagnosis codes used in the analysis of our CD cohort
Crohn’s disease: D62160
Ileum or ileocecal: T65200, T65500T67000, T65500, M81406
Resection: P11100, P11200, P11101
Gallbladder: T57000
Adenocarcinoma M81403
Metastasis, adenocarcinoma M81406
Metastasis, carcinoma M80106
Intramucosal carcinoma M80105
PALGA codes used to extract cholecystectomy rates in general Dutch population
Cholecystectomy: T57000111000
Gallbladder and excision: T57___ AND *54*
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Goet, J.C., Beelen, E.M.J., Biermann, K.E. et al. Cholecystectomy Risk in Crohn’s Disease Patients After Ileal Resection: a Long-term Nationwide Cohort Study. J Gastrointest Surg 23, 1840–1847 (2019). https://doi.org/10.1007/s11605-018-4028-y
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DOI: https://doi.org/10.1007/s11605-018-4028-y