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Dive into the research topics where J Vanwalleghem is active.

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Featured researches published by J Vanwalleghem.


Transplantation | 1999

Differences in gastric motor activity in renal transplant recipients treated with FK-506 versus cyclosporine

Bart Maes; J Vanwalleghem; Dirk Kuypers; Yvo Ghoos; Paul Rutgeerts; Yves Vanrenterghem

BACKGROUND Little is known concerning gastric motility after renal transplantation and on the impact of immunosuppressants on gastric emptying. METHODS Gastric emptying was measured in renal transplant recipients, taking different immunosuppressive therapy (steroids and cyclosporine/azathioprine/FK-506), and compared with normal volunteers. RESULTS After renal transplantation, gastric emptying of liquids was normal, irrespective of the type of immunosuppression. However, solid gastric emptying was significantly faster in FK-506-treated patients compared with patients taking cyclosporine for all measured emptying parameters. Compared with normal volunteers solid gastric emptying was slower in patients taking cyclosporine, comparable in azathioprine treated patients, and characterized by an unusual short lag phase in patients taking FK-506. CONCLUSIONS In stable renal transplant recipients gastric emptying of solids was significantly faster in patients on FK-506 compared with patients taking cyclosporine. Therefore, FK-506 may be the immunosuppressant of choice after solid organ transplantation in patients with problems related to gastroparesis.


American Journal of Kidney Diseases | 2009

Immunogenicity of a Standard Trivalent Influenza Vaccine in Patients on Long-term Hemodialysis: An Open-Label Trial

Johan Scharpé; Willy Peetermans; J Vanwalleghem; Bart Maes; Bert Bammens; Kathleen Claes; André D. Osterhaus; Yves Vanrenterghem; Pieter Evenepoel

BACKGROUND Disturbances in acquired immunity are considered to be responsible, at least in part, for the high infection rate and inadequate response to vaccinations observed in hemodialysis (HD) patients. The present prospective trial aimed to: (1) evaluate the immunogenicity of a standard influenza vaccine in HD patients, and (2) identify determinants of the immune response. STUDY DESIGN Prospective interventional open-label study. SETTING & PARTICIPANTS 201 long-term HD patients and 41 healthy volunteers. INTERVENTION Vaccination with a standard trivalent inactivated influenza vaccine. OUTCOMES The primary outcome was seroprotection rate, defined as percentage of participants with an antibody titer of 40 or greater 1 month after vaccination. MEASUREMENTS All antibody titers were determined in duplicate by using the hemagglutination inhibition assay. Regression analyses were performed to investigate the association between demographics, uremic retention solutes (including p-cresol), inflammation, nutrition, iron status, trace elements, and immune response in HD patients. RESULTS More than 80% of HD patients showed seroprotection after vaccination. The immune response of HD patients was similar to that of healthy volunteers. Booster vaccination did not improve the immune response. High serum ferritin level was the only parameter independently associated with a better vaccination-induced antibody response in HD patients. LIMITATIONS A high seroprotection rate at baseline undermined the power to identify clinical determinants of the immune response. CONCLUSIONS Influenza vaccination is as efficacious in HD patients as in healthy volunteers. With the exception of serum ferritin, none of the investigated parameters of nutrition, inflammation, and dialysis adequacy had a significant impact on the immune response. Our data support annual vaccination of HD patients and question the clinical relevance of disturbances in acquired immunity in contemporary HD patients.


Transplantation | 1998

Inferior outcome of cadaveric kidneys preserved for more than 24 hr in histidine-tryptophan-ketoglutarate solution. Leuven Collaborative Group for Transplantation.

L Roels; Willy Coosemans; J Donck; Bart Maes; J Peeters; J Vanwalleghem; Jacques Pirenne; Yves Vanrenterghem

BACKGROUND During recent years, an increasing number of transplant centers within the Eurotransplant organization have used histidine-tryptophan-ketoglutarate (HTK) solution instead of University of Wisconsin (UW) solution as their preferred cold storage solution for abdominal organ preservation. We report on our single-center experience on the outcome of imported kidneys preserved with either HTK or UW solution in relation to the duration of cold ischemia time (CIT). METHODS Between July 1989 and July 1997, 323 cadaveric kidneys preserved with UW or HTK and imported as a result of an exchange within the Eurotransplant organization were transplanted at our institution. CIT was <24 hr in 216 kidneys (UW: n=174, HTK: n=42) and > or =24 hr in 107 kidneys (UW: n=67, HTK: n=40). Renal functional outcome was evaluated by comparing delayed graft function and initial non-function rates, daily urinary output, the evolution of serum creatinine, and creatinine clearance at 1, 3, 5, 7, and 14 days and at 1, 3, 6 and 12 months, and graft survival at 1 year after transplantation in relation to the type of cold storage solution and CIT < or > or =24 hr. RESULTS Whereas the incidence of delayed graft function did not differ significantly between kidneys preserved for less than 24 hr in UW (18.6%) or HTK (26.2%), this rate increased to 50% in HTK kidneys compared to 23.9% in UW kidneys when CIT exceeded 24 hr (P=0.006). Mean serum creatinine and creatinine clearance values were better at 1 and 5 days postoperatively in kidneys preserved <24 hr with UW as compared to HTK (P<0.05). After 24 hr of CIT, HTK-preserved kidneys showed an impaired renal function, not only in the immediate postoperative phase but also at 1, 3, 6, and 12 months after transplantation (P<0.05). Graft survival at 1 year was 92.9% in UW vs. 87.5% in HTK kidneys preserved for <24 hr (NS), and 91% vs. 77.4% when CIT exceeded 24 hr (P=0.059). CONCLUSIONS From these single-center findings, it can be concluded that UW is superior to HTK in kidney preservation, particularly when CIT exceeds 24 hr.


American Journal of Kidney Diseases | 1999

IgA antiglomerular basement membrane disease associated with bronchial carcinoma and monoclonal gammopathy

Bart Maes; J Vanwalleghem; Dirk Kuypers; Boudewijn Van Damme; Marc Waer; Yves Vanrenterghem

Antiglomerular basement membrane (anti-GBM) disease is characterized by a linear deposition of immunoglobulins along the glomerular basement membrane. A 67-year-old man with a recently discovered monoclonal gammopathy of unknown significance (MGUS) presented with microscopic hematuria, nephrotic-range proteinuria, and rapidly deteriorating renal function after a pneumonia. Renal histology showed a crescentic glomerulonephritis; immunohistology showed intense linear staining of the GBM with immunoglobulin A (IgA) and moderate linear staining with kappa and lambda light chains. Screening for systemic disease, including diabetes mellitus, lupus erythematodes disseminatus, cryoglobulinemia, was negative. Serological tests for detection of anti-GBM antibodies were positive for IgA class and negative for IgG. Further examination indicated a bronchial carcinoma T2N2M0. This clinical report adds new information to the spectrum of anti-GBM disease and suggests that neoplasia may be associated with unusual exposure of and/or immune response to epitopes in the GBM.


Ndt Plus | 2018

Haemodynamic or metabolic stimulation tests to reveal the renal functional response: requiem or revival?

Bart De Moor; J Vanwalleghem; Quirine Swennen; Koen Stas; Björn Meijers

ABSTRACT Renal stimulation tests document the dynamic response of the glomerular filtration rate (GFR) after a single or a combination of stimuli, such as an intravenous infusion of dopamine or amino acids or an oral protein meal. The increment of the GFR above the unstimulated state has formerly been called the renal functional reserve (RFR). Although the concept of a renal reserve capacity has not withstood scientific scrutiny, the literature documenting renal stimulation merits renewed interest. An absent or a blunted response of the GFR after a stimulus indicates lost or diseased nephrons. This information is valuable in preventing, diagnosing and prognosticating acute kidney injury and pregnancy-related renal events as well as chronic kidney disease. However, before renal function testing is universally practiced, some shortcomings must be addressed. First, a common nomenclature should be decided upon. The expression of RFR should be replaced by renal functional response. Second, a simple protocol must be developed and propagated. Third, we suggest designing prospective studies linking a defective stimulatory response to emergence of renal injury biomarkers, to histological or morphological renal abnormalities and to adverse renal outcomes in different renal syndromes.


Kidney International | 2004

Mycophenolate mofetil in IgA nephropathy: Results of a 3-year prospective placebo-controlled randomized study

Bart Maes; Raymond Oyen; Kathleen Claes; Pieter Evenepoel; Dirk Kuypers; J Vanwalleghem; Boudewijn Van Damme; Yves Vanrenterghem


Nephrology Dialysis Transplantation | 2004

The value of tuberculin skin testing in haemodialysis patients

Anne Wauters; Willy Peetermans; Paul Van den Brande; Bart De Moor; Pieter Evenepoel; Hilde Keuleers; Dirk Kuypers; Koen Stas; J Vanwalleghem; Yves Vanrenterghem; Bart Maes


American Journal of Kidney Diseases | 2002

Regional citrate anticoagulation for hemodialysis using a conventional calcium-containing dialysate

Pieter Evenepoel; Bart Maes; J Vanwalleghem; Dirk Kuypers; T Messiaen; Yves Vanrenterghem


Nephrology Dialysis Transplantation | 2001

Trisodium citrate 30% vs heparin 5% as catheter lock in the interdialytic period in twin‐ or double‐lumen dialysis catheters for intermittent haemodialysis

Koenraad J. F. Stas; J Vanwalleghem; Bart De Moor; Hilde Keuleers


Transplantation Proceedings | 1999

Impact of early vesico ureteral reflux on the transplanted kidney.

Willy Coosemans; Filip Rega; L Roels; J Peeters; J Donck; J Vanwalleghem; Bart Maes; Yves Vanrenterghem; Jacques Pirenne

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Yves Vanrenterghem

Katholieke Universiteit Leuven

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Bart Maes

Katholieke Universiteit Leuven

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Dirk Kuypers

Katholieke Universiteit Leuven

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Willy Coosemans

Katholieke Universiteit Leuven

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Jacques Pirenne

Katholieke Universiteit Leuven

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Pieter Evenepoel

Katholieke Universiteit Leuven

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J Peeters

Katholieke Universiteit Leuven

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J Donck

Katholieke Universiteit Leuven

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Willy Peetermans

Katholieke Universiteit Leuven

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