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Dive into the research topics where I. S. Bakker is active.

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Featured researches published by I. S. Bakker.


British Journal of Surgery | 2014

Risk factors for anastomotic leakage and leak-related mortality after colonic cancer surgery in a nationwide audit

I. S. Bakker; Irene Grossmann; D. Henneman; Klaas Havenga; Theo Wiggers

Surgical resection with restoration of bowel continuity is the cornerstone of treatment for patients with colonic cancer. The aim of this study was to identify risk factors for anastomotic leakage (AL) and subsequent death after colonic cancer surgery.


Colorectal Disease | 2016

High mortality rates after nonelective colon cancer resection: results of a national audit.

I. S. Bakker; H.S. Snijders; I. Grossmann; T. M. Karsten; Klaas Havenga; Theo Wiggers

Colon cancer resection in a nonelective setting is associated with high rates of morbidity and mortality. The aim of this retrospective study is to identify risk factors for overall mortality after colon cancer resection with a special focus on nonelective resection.


BMC Surgery | 2012

The C-seal trial: colorectal anastomosis protected by a biodegradable drain fixed to the anastomosis by a circular stapler, a multi-center randomized controlled trial

I. S. Bakker; A. N. Morks; Henk O. ten Cate Hoedemaker; Johannes G. M. Burgerhof; Henri G. D. Leuvenink; Rutger J. Ploeg; Klaas Havenga

BackgroundAnastomotic leakage is a major complication in colorectal surgery and with an incidence of 11% the most common cause of morbidity and mortality. In order to reduce the incidence of anastomotic leakage the C-seal is developed. This intraluminal biodegradable drain is stapled to the anastomosis with a circular stapler and prevents extravasation of intracolonic content in case of an anastomotic dehiscence.The aim of this study is to evaluate the efficacy of the C-seal in reducing anastomotic leakage in stapled colorectal anastomoses, as assessed by anastomotic leakage leading to invasive treatment within 30 days postoperative.MethodsThe C-seal trial is a prospective multi-center randomized controlled trial with primary endpoint, anastomotic leakage leading to re-intervention within 30 days after operation. In this trial 616 patients will be randomized to the C-seal or control group (1:1), stratified by center, anastomotic height (proximal or distal of peritoneal reflection) and the intention to create a temporary deviating ostomy. Interim analyses are planned after 50% and 75% of patient inclusion. Eligible patients are at least 18 years of age, have any colorectal disease requiring a colorectal anastomosis to be made with a circular stapler in an elective setting, with an ASA-classification < 4. Oral mechanical bowel preparation is mandatory and patients with signs of peritonitis are excluded. The C-seal student team will perform the randomization procedure, supports the operating surgeon during the C-seal application and achieves the monitoring of the trial. Patients are followed for one year after randomization en will be analyzed on an intention to treat basis.DiscussionThis Randomized Clinical trial is designed to evaluate the effectiveness of the C-seal in preventing clinical anastomotic leakage.Trial registrationNTR3080


British Journal of Surgery | 2017

Randomized clinical trial of biodegradeable intraluminal sheath to prevent anastomotic leak after stapled colorectal anastomosis

I. S. Bakker; A. N. Morks; H. O. ten Cate Hoedemaker; Johannes G. M. Burgerhof; Henri G. D. Leuvenink; J. B. van Praagh; Rutger J. Ploeg; Klaas Havenga

Anastomotic leakage is a potential major complication after colorectal surgery. The C‐seal was developed to help reduce the clinical leakage rate. It is an intraluminal sheath that is stapled proximal to a colorectal anastomosis, covering it intraluminally and thus preventing intestinal leakage in case of anastomotic dehiscence. The C‐seal trial was initiated to evaluate the efficacy of the C‐seal in reducing anastomotic leakage in stapled colorectal anastomoses.


International Journal of Surgery Case Reports | 2013

A very late recurrence of a formerly misdiagnosed low grade endometrial stromal sarcoma metastasized to the colon

I. S. Bakker; Miriam L. Hoven-Gondrie; Freek C.P. Moll; Harm H. de Haan

INTRODUCTION Endometrial stromal sarcomas are rare mesenchymal neoplasms of the uterus with an indolent clinical course but a high risk of recurrence. PRESENTATION OF CASE We report a case of a 78 year old woman who presented with rectal bleeding and recurrent urinary tract infections, caused by a very late recurrence of a formerly misdiagnosed low grade endometrial stromal sarcoma, metastasized to the colon. DISCUSSION Endometrial stromal sarcomas are difficult to diagnose, both due to the rarity of the tumor and because of the close resemblance of the tumor to normal stromal tissue. These tumors are known for a high tendency of recurrence, therefore long term follow up is required in patients with endometrial stromal sarcoma. CONCLUSION In patients with a history known for endometrial stromal sarcoma recurrence should always be considered.


Annals of Surgery | 2018

Mucus Microbiome of Anastomotic Tissue During Surgery Has Predictive Value for Colorectal Anastomotic Leakage.

Jasper van Praagh; Marcus C. de Goffau; I. S. Bakker; Harry van Goor; Hermie J. M. Harmsen; Peter Olinga; Klaas Havenga

Objective: The aim of the present study is to investigate the association of gut microbiota, depending on treatment method, with the development of colorectal anastomotic leakage (AL). Background: AL is a major cause for morbidity and mortality after colorectal surgery, but the mechanism behind this complication still is not fully understood. Methods: Bacterial DNA was isolated from 123 “donuts” of patients where a stapled colorectal anastomosis was made and was analyzed using 16S MiSeq sequencing. In 63 patients, this anastomosis was covered with a C-seal, a bioresorbable sheath stapled to the anastomosis. Results: In non-C-seal patients, AL development was associated with low microbial diversity (P = 0.002) and correspondingly with a high abundance of the dominant Bacteroidaceae and Lachnospiraceae families (P = 0.008 and 0.010, respectively). In C-seal samples, where AL rates were slightly higher (25% vs 17%), an association with the gut microbiota composition was almost undetectable. Only a few opportunistic pathogenic groups of low abundance were associated with AL in C-seal patients, in particular Prevotella oralis (P = 0.007). Conclusions: AL in patients without a C-seal can be linked to the intestinal microbiota, in particular with a low microbial diversity and a higher abundance of especially mucin-degrading members of the Bacteroidaceae and Lachnospiraceae families. In C-seal patients, however, it seems that any potential protective benefits or harmful consequences of the gut microbiota composition in regard to wound healing are negated, as progression to AL is independent of the initially dominant bacterial composition.


International Journal of Colorectal Disease | 2018

Stercoral perforation proximal to the stapled anastomosis after low anterior resection with an intraluminal device

J. B. van Praagh; I. S. Bakker; Klaas Havenga

Stercoral perforation of the colon is a rare phenomenon and a potential life-threatening condition requiring acute intervention. A little more than 200 cases have been described to date. The mechanism is not completely understood. In this short communication, we present three patients with a colon perforation proximal to the anastomosis, similar to a stercoral perforation, following colorectal cancer resection with application of an intraluminal device, the C-seal.


Gastroenterology | 2016

Sa2007 Intestinal Microbiota and Anastomotic Leakage of Stapled Colorectal Anastomoses

Jasper van Praagh; Marcus C. de Goffau; I. S. Bakker; Hermie J. M. Harmsen; Peter Olinga; Klaas Havenga

Background Anastomotic leakage (AL) after colorectal surgery is a severe complication, resulting in morbidity, reinterventions, prolonged hospital stay and, in some cases, death. Some technical and patient-related aetiological factors of AL are well established. In many cases, however, none of these factors seem to explain the occurrence of AL. Recent studies suggest that the intestinal microbiome plays a role in wound healing, diabetes and Crohn’s disease. The aim of this study was to compare the intestinal microbiota of patients who developed AL with matched patients with healed colorectal anastomoses. Methods We investigated the microbiome in the doughnuts collected from 16 patients participating in the C-seal trial. We selected eight patients who developed AL requiring reintervention and eight matched controls without AL. We analysed the bacterial 16S rDNA of both groups with MiSeq sequencing. Results The abundance of Lachnospiraceae is statistically higher (P = 0.001) in patient group who did develop AL, while microbial diversity levels were higher in the group who did not develop AL (P = 0.037). Body mass index (BMI) was also positively associated with the abundance of the Lachnospiraceae family (P = 0.022). Conclusion A correlation between the bacterial family Lachnospiraceae, low microbial diversity and anastomotic leakage, possibly in association with the BMI, was found. The relative abundance of the Lachnospiraceae family is possibly explained by the higher abundance of mucin-degrading Ruminococci within that family in AL cases (P = 0.011) as is similarly the case in IBD.


Surgical Endoscopy and Other Interventional Techniques | 2016

Intestinal microbiota and anastomotic leakage of stapled colorectal anastomoses: a pilot study

Jasper van Praagh; Marcus C. de Goffau; I. S. Bakker; Hermie J. M. Harmsen; Peter Olinga; Klaas Havenga


Ejso | 2016

100. Prevention of anastomotic leakage in stapled colorectal anastomoses: Results of the multi-center randomized controlled C-seal trial

I. S. Bakker; A. N. Morks; H.O. ten Cate Hoedemaker; Johannes G. M. Burgerhof; Henri G. D. Leuvenink; J. B. van Praagh; Rutger J. Ploeg; Klaas Havenga

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Klaas Havenga

University Medical Center Groningen

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A. N. Morks

University Medical Center Groningen

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Henri G. D. Leuvenink

University Medical Center Groningen

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Hermie J. M. Harmsen

University Medical Center Groningen

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J. B. van Praagh

University Medical Center Groningen

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Johannes G. M. Burgerhof

University Medical Center Groningen

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Marcus C. de Goffau

University Medical Center Groningen

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Peter Olinga

University of Groningen

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