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Dive into the research topics where Olivier R. Busch is active.

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Featured researches published by Olivier R. Busch.


The New England Journal of Medicine | 2011

Pneumatic dilation versus laparoscopic Heller's myotomy for idiopathic achalasia.

Guy E. Boeckxstaens; Vito Annese; Stanislas Bruley des Varannes; Stanislas Chaussade; Mario Costantini; Antonello Cuttitta; J. Ignasi Elizalde; Uberto Fumagalli; Marianne Gaudric; Wout O. Rohof; André Smout; Jan Tack; Aeilko H. Zwinderman; Giovanni Zaninotto; Olivier R. Busch

BACKGROUNDnMany experts consider laparoscopic Hellers myotomy (LHM) to be superior to pneumatic dilation for the treatment of achalasia, and LHM is increasingly considered to be the treatment of choice for this disorder.nnnMETHODSnWe randomly assigned patients with newly diagnosed achalasia to pneumatic dilation or LHM with Dors fundoplication. Symptoms, including weight loss, dysphagia, retrosternal pain, and regurgitation, were assessed with the use of the Eckardt score (which ranges from 0 to 12, with higher scores indicating more pronounced symptoms). The primary outcome was therapeutic success (a drop in the Eckardt score to ≤3) at the yearly follow-up assessment. The secondary outcomes included the need for retreatment, pressure at the lower esophageal sphincter, esophageal emptying on a timed barium esophagogram, quality of life, and the rate of complications.nnnRESULTSnA total of 201 patients were randomly assigned to pneumatic dilation (95 patients) or LHM (106). The mean follow-up time was 43 months (95% confidence interval [CI], 40 to 47). In an intention-to-treat analysis, there was no significant difference between the two groups in the primary outcome; the rate of therapeutic success with pneumatic dilation was 90% after 1 year of follow-up and 86% after 2 years, as compared with a rate with LHM of 93% after 1 year and 90% after 2 years (P=0.46). After 2 years of follow-up, there was no significant between-group difference in the pressure at the lower esophageal sphincter (LHM, 10 mm Hg [95% CI, 8.7 to 12]; pneumatic dilation, 12 mm Hg [95% CI, 9.7 to 14]; P=0.27); esophageal emptying, as assessed by the height of barium-contrast column (LHM, 1.9 cm [95% CI, 0 to 6.8]; pneumatic dilation, 3.7 cm [95% CI, 0 to 8.8]; P=0.21); or quality of life. Similar results were obtained in the per-protocol analysis. Perforation of the esophagus occurred in 4% of the patients during pneumatic dilation, whereas mucosal tears occurred in 12% during LHM. Abnormal exposure to esophageal acid was observed in 15% and 23% of the patients in the pneumatic-dilation and LHM groups, respectively (P=0.28).nnnCONCLUSIONSnAfter 2 years of follow-up, LHM, as compared with pneumatic dilation, was not associated with superior rates of therapeutic success. (European Achalasia Trial Netherlands Trial Register number, NTR37, and Current Controlled Trials number, ISRCTN56304564.).


Journal of Gastrointestinal Surgery | 2010

Endoscopic and Percutaneous Preoperative Biliary Drainage in Patients with Suspected Hilar Cholangiocarcinoma

Jaap J. Kloek; Niels A. van der Gaag; Yalda Aziz; Erik A. J. Rauws; Otto M. van Delden; Johan S. Laméris; Olivier R. Busch; Dirk J. Gouma; Thomas M. van Gulik

IntroductionControversy exists over the preferred technique of preoperative biliary drainage (PBD) in patients with hilar cholangiocarcinoma (HCCA) requiring major liver resection. The current study compared outcomes of endoscopic biliary drainage (EBD) and percutaneous transhepatic biliary drainage (PTBD) in patients with resectable HCCA.MethodsOne hundred fifteen consecutive patients were explored for HCCA between 2001 and July 2008 and assigned by initial PBD procedure to either EBD or PTBD.ResultsOf these patients, 101 (88%) underwent PBD; 90 patients underwent EBD as primary procedure, and 11 PTBD. The technical success rate of initial drainage was 81% in the EBD versus 100% in the PTBD group (Pu2009=u20090.20). Stent dislocation was similar in the EBD and PTBD groups (23% vs. 20%, Pu2009=u20090.70). Infectious complications were significantly more common in the endoscopic group (48% vs. 9%, Pu2009<u20090.05). Patients in the EBD group underwent more drainage procedures (2.8 vs. 1.4, Pu2009<u20090.01) and had a significantly longer drainage period until laparotomy (mean 15xa0weeks vs. 11xa0weeks in the PTBD group; Pu2009<u20090.05). In 30 patients, EBD was converted to PTBD due to failure of the endoscopic approach.ConclusionsPreoperative percutaneous drainage could outperform endoscopic stent placement in patients with resectable HCCA, showing fewer infectious complications, using less procedures.


Annals of Surgery | 2011

Fluorodeoxyglucose Positron Emission Tomography for Evaluating Early Response During Neoadjuvant Chemoradiotherapy in Patients With Potentially Curable Esophageal Cancer

Mark van Heijl; Jikke M. T. Omloo; Mark I. van Berge Henegouwen; Otto S. Hoekstra; Ronald Boellaard; Patrick M. Bossuyt; Olivier R. Busch; Hugo W. Tilanus; Maarten C. C. M. Hulshof; Ate van der Gaast; G.A.P. Nieuwenhuijzen; Han J. Bonenkamp; John Plukker; Miguel A. Cuesta; Fiebo J. ten Kate; Jan Pruim; Herman van Dekken; Jacques J. Bergman; Gerrit W. Sloof; J. Jan B. van Lanschot

Background:Neoadjuvant chemoradiotherapy before surgery can improve survival in patients with potentially curable esophageal cancer, but not all patients respond. Fluorodeoxyglucose positron emission tomography (FDG-PET) has been proposed to identify nonresponders early during neoadjuvant chemoradiotherapy. The aim of the present study was to determine whether FDG-PET could differentiate between responding and nonresponding esophageal tumors early in the course of neoadjuvant chemoradiotherapy. Methods:This clinical trial comprised serial FDG-PET before and 14 days after start of chemoradiotherapy in patients with potentially curable esophageal carcinoma. Histopathologic responders were defined as patients with no or less than 10% viable tumor cells (Mandard score on resection specimen). PET response was measured using the standardized uptake value (SUV). Receiver operating characteristic analysis was used to evaluate the ability of SUV in distinguishing between histopathologic responders and nonresponders. Results:In 100 included patients, 64 were histopathologic responders. The median SUV decrease 14 days after the start of therapy was 30.9% for histopathologic responders and 1.7% for nonresponders (P = 0.001). In receiver operating characteristic analysis, the area under the curve was 0.71 (95% CI = 0.60–0.82). Using a 0% SUV decrease cutoff value, PET correctly identified 58 of 64 responders (sensitivity 91%) and 18 of 36 nonresponders (specificity 50%). The corresponding positive and negative predictive values were 76% and 75%, respectively. Conclusions:SUV decrease 14 days after the start of chemoradiotherapy was significantly associated with histopathologic tumor response, but its accuracy in detecting nonresponders was too low to justify the clinical use of FDG-PET for early discontinuation of neoadjuvant chemoradiotherapy in patients with potentially curable esophageal cancer.


British Journal of Surgery | 2014

Impact of centralization of pancreatic cancer surgery on resection rates and survival

G.A. Gooiker; Valery Lemmens; Marc G. Besselink; Olivier R. Busch; Bert A. Bonsing; I.Q. Molenaar; R.A.E.M. Tollenaar; I. H. J. T. de Hingh; Michel W.J.M. Wouters

Centralization of pancreatic surgery has been shown to reduce postoperative mortality. It is unknown whether resection rates and survival have also improved. The aim of this study was to analyse the impact of nationwide centralization of pancreatic surgery on resection rates and long‐term survival.


Gastrointestinal Endoscopy | 2011

Do we still need EUS in the workup of patients with early esophageal neoplasia? A retrospective analysis of 131 cases

Roos E. Pouw; Noor Heldoorn; Lorenza Alvarez Herrero; Fiebo J. ten Kate; Mike Visser; Olivier R. Busch; Mark I. van Berge Henegouwen; Kausilia K. Krishnadath; Bas L. Weusten; Paul Fockens; Jacques J. Bergman

BACKGROUNDnEUS is often used for locoregional staging of early esophageal neoplasia. However, its value compared with that of endoscopic examination and diagnostic endoscopic resection (ER) may be questioned because diagnostic ER allows histological assessment of submucosal invasion and other risk factors for lymph node metastasis, eg, poor differentiation/lymphovascular invasion.nnnOBJECTIVEnTo evaluate how often patients were excluded from endoscopic treatment of esophageal neoplasia based on EUS findings.nnnDESIGNnRetrospective cohort study.nnnSETTINGnTertiary care institution.nnnPATIENTSnPatients with early esophageal neoplasia.nnnINTERVENTIONSnEUS, diagnostic ER.nnnMAIN OUTCOME MEASUREMENTSnNumber of patients excluded from endoscopic treatment based on EUS results.nnnRESULTSnA total of 131 patients were included (98 men, 33 women; age 66 ± 13 years). In 105 of 131 patients (80%), EUS findings were unremarkable. In 25 of 105 patients (24%), diagnostic ER showed submucosal invasion (n = 17), deep resection margins positive for cancer (n = 2, confirmed at surgery), or poor differentiation/lymphovascular invasion (n = 6). In 26 of 131 patients (20%), EUS findings raised the suspicion of submucosal invasion and/or lymph node metastasis. In the 14 of 26 patients (54%) with abnormal EUS findings, endoscopy results were unremarkable. Diagnostic ER showed submucosal invasion in 7 of 14 (50%) patients, whereas no lymph node metastasis risk factors were found in 7 of 14 patients (50%), who subsequently underwent curative endoscopic treatment. In 12 of 26 patients (46%) with abnormal EUS, endoscopy also raised doubts on whether curative endoscopic treatment could be achieved. After diagnostic ER, no risk factors for lymph node metastasis were found in 3 of 12 patients (25%).nnnLIMITATIONnRetrospective study.nnnCONCLUSIONSnThis study shows that EUS has virtually no clinical impact on the workup of early esophageal neoplasia and strengthens the role of diagnostic ER as a final diagnostic step.


The Annals of Thoracic Surgery | 2008

Preoperative Prediction of the Occurrence and Severity of Complications After Esophagectomy for Cancer With Use of a Nomogram

Sjoerd M. Lagarde; Johannes B. Reitsma; Anna-Karin D. Maris; Mark I. van Berge Henegouwen; Olivier R. Busch; Hugo Obertop; Aelko H. Zwinderman; J. Jan B. van Lanschot

BACKGROUNDnPredicting the severity of complications after esophagectomy may supply important information for both patient and surgeon. The aim of the present study was to develop a nomogram based on preoperative risk factors to predict the severity of complications in patients who undergo esophagectomy for cancer.nnnMETHODSnA consecutive series of 663 patients who underwent esophagectomy between January 1993 and August 2005 was used to develop a prognostic model. The model was validated in a second group of patients who were operated between August 2005 and November 2006. Ordinal logistic regression analysis was performed to predict the severity of complications. Diverse simple and conventional preoperative risk factors were evaluated. A nomogram was developed to enhance clinical applicability.nnnRESULTSnPatients were divided into three complication categories: those who suffered from no complications (n = 197); minor complications (n = 354); and major complications (n = 112). The following predictors remained in the model after multivariate analysis: higher age (p = 0.014); cerebrovascular accident/transient ischemic attack (CVA/TIA) (p = 0.009) or myocardial infarction in the medical history (p = 0.066); lower forced expiratory volume in the first second of expiration (FEV(1)) (p = 0.030); presence of electrocardiogram-changes (p = 0.008); and more extensive surgery (p < 0.001). A nomogram based on these variables was constructed. Overall agreement between the predicted probabilities and the observed frequencies was good in the development and the validation set.nnnCONCLUSIONSnThe nomogram predicts the severity of complications for individual patients and may help in informing the patient before undergoing esophagectomy for cancer and in choosing the optimal extent of surgery. When externally validated, the nomogram may play a role in risk-adjusted audit of morbidity after esophagectomy.


Liver International | 2006

Management of spontaneous haemorrhage and rupture of hepatocellular adenomas. A single centre experience

Deha Erdogan; Olivier R. Busch; Otto M. van Delden; Fiebo J. ten Kate; Dirk J. Gouma; Thomas M. van Gulik

Abstract: Background: Hepatocellular adenomas (HCA) may present with spontaneous haemorrhage and rupture. The aim of this study was to assess management in 22 patients treated for haemorrhage and/or rupture of HCA.


Surgical Endoscopy and Other Interventional Techniques | 2004

Robot-assisted laparoscopic cholecystectomy versus conventional laparoscopic cholecystectomy: a comparative study

D. Nio; W. A. Bemelman; Olivier R. Busch; B. C. Vrouenraets; D. J. Gouma

Background: The efficacy of conventional laparoscopic cholecystectomy (CLC) was compared with robot-assisted laparoscopic cholecystectomy (RLC). Surgical trainees performed the LC to avoid the surgeon’s experience bias. Methods: Two surgical trainees performed 10 CLCs and 10 RLCs at random with a Zeus-Aesop Surgical Robotic System. The primary efficacy parameters were the total time and the number of actions involved in the procedure. The secondary parameters were setup and dissection times, and the number of grasping and dissection actions. Surgical complications were evaluated. Results: For CLC and RLC, respectively, the total times were 95.4 ± 28 min and 123.5 ± 33.3 min and the total actions were 420 ± 176.3 and 363.5 ± 158.2. For CLC, the times required for setup (21 ± 10.4 min) and dissection (50.2 ± 17.7 min) were less than for RLC (33.8 ± 11.3 min and 72 ± 24.3 min, respectively). The numbers of grasping and dissection actions were not significantly different: 41.4 ± 26.5 and 378 ± 173.7, respectively, for CLC versus 48.9 ± 27 and 314.6 ± 141.9, respectively, for RLC. Conclusion: Although feasible, RLC requires significantly more time than CLC because of slower performed actions.


Archives of Surgery | 2012

Clinical outcome in relation to timing of surgery in chronic pancreatitis: a nomogram to predict pain relief

Usama Ahmed Ali; Vincent B. Nieuwenhuijs; Casper H.J. van Eijck; Hein G. Gooszen; Ronald M. van Dam; Olivier R. Busch; Marcel G. W. Dijkgraaf; Femke A. Mauritz; Sjoerd Jens; Jay Mast; Harry van Goor; Marja A. Boermeester

OBJECTIVEnTo evaluate the effect of timing of surgery on the long-term clinical outcome of surgery in chronic pancreatitis (CP).nnnDESIGNnCohort study with long-term follow-up.nnnSETTINGnFive specialized academic centers.nnnPATIENTSnPatients with CP treated surgically for pain.nnnINTERVENTIONSnPancreatic resection and drainage procedures for pain relief.nnnMAIN OUTCOME MEASURESnPain relief (pain visual analogue score ≤4), pancreatic function, and quality of life.nnnRESULTSnWe included 266 patients with median follow-up of 62 months (interquartile range, 31-112). Results were presented as odds ratios (ORs)with 95% confidence intervals after correction for bias using bootstrap-corrected analysis. Pain relief was achieved in 149 patients (58%). Surgery within 3 years of symptoms was independently associated with more pain relief (OR, 1.8; 95% CI, 1.0-3.4; P = .03) and less endocrine pancreatic insufficiency (OR, 0.57; 95% CI, 0.33-0.96; P = .04). More pain relief was also observed in patients not taking opioids preoperatively (OR, 2.1; 95% CI, 1.2-4.0; P = .006) and who had 5 or fewer endoscopic treatments prior to surgery (OR, 2.5; 95% CI, 1.1-6.3; P = .04). The probability of achieving pain relief varied between 23% and 75%, depending on these risk factors.nnnCONCLUSIONSnThe timing of surgery is an important risk factor for clinical outcome in CP. Surgery may need to be considered at an earlier phase than it is now, preferably within 3 years of symptomatic CP. Likelihood of postoperative pain relief can be calculated on an individual basis using the presented nomogram.


Diseases of The Colon & Rectum | 2003

Feasibility of early closure of loop ileostomies: a pilot study.

Roel Bakx; Olivier R. Busch; Dirk van Geldere; Willem A. Bemelman; J. Frederik M. Slors; J. Jan B. van Lanschot

PurposeA loop ileostomy is constructed to protect a distal anastomosis, and closure is usually performed not earlier than after two to three months. Earlier closure might reduce stoma-related morbidity, improve quality of life, and still effectively protect the distal anastomosis. This pilot study was designed to investigate the feasibility of early closure of loop ileostomies, i.e., during the same hospital admission as the initial operation. METHODS: Twenty-seven consecutive patients with a protective loop ileostomy were included. If patient’s recovery was uneventful, water-soluble contrast enema examination was performed, preferably after seven to eight days. If no radiologie signs of leakage were detected, the ileostomy was closed during the same hospital admission. RESULTS: Twenty-seven patients (8 females; mean age, 60 years) were analyzed. Eighteen patients had early ileostomy closure on average 11 (range, 7-21) days after the initial procedure. In nine patients the procedure was postponed because of leakage of the anastomosis (n = 3), delayed recovery (n = 1), small bowel obstruction (n = 1), gastroparesis (n = 1), logistic reasons (n = 2), or irradical cancer resection followed by radiotherapy (n = 1). There was no mortality and four mild complications occurred after early closure: superficial wound infection (n = 2), intravenous-catheter sepsis (n = 1), small bowel obstruction (n = 1). CONCLUSION: Closure of a loop ileostomy early after the initial operation was feasible in 18 of 27 patients and was associated with low morbidity and no mortality.

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Bas Groot Koerkamp

Erasmus University Rotterdam

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