Koen Van Herck

Dr. Koen Van Herck

Belgian Cancer Registry (BCR), Brussels, Brussels-Capital Region, Belgium
orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2007 in The Lancet
Verified
Journal Article
Closed access
SMSurbhi Malhotra-Kumar
Surbhi Malhotra-Kumar
CLChristine Lammens
Christine Lammens
Samuel CoenenSamuel Coenen
Samuel Coenen
KHKoen Van Herck
Koen Van Herck
HGHerman Goossens
Herman Goossens

1 January 2004 in Journal of Travel Medicine
Verified
Journal Article
Open access
PDF file
KHKoen Van Herck
Koen Van Herck
Francesco CastelliFrancesco Castelli
Francesco Castelli
JZJane Zuckerman
Jane Zuckerman
HNHans Nothdurft
Hans Nothdurft
PDPierre Van Damme
Pierre Van Damme
RSRobert Steffen
Robert Steffen
Background. The European Travel Health Advisory Board conducted a cross-sectional pilot survey to evaluate current travel health knowledge, attitudes a

1 September 2003 in The Lancet
Verified
Journal Article
Closed access
PDPierre Van Damme
Pierre Van Damme
JBJ Banatvala
J Banatvala
OFO Fay
O Fay
SIS Iwarson
S Iwarson
BMB McMahon
B McMahon
FSF Von Sonnenburg
F Von Sonnenburg

1 December 2009 in Gynecologic Oncology
Verified
Journal Article
Closed access
MDMarie-Pierre David
Marie-Pierre David
KHKoen Van Herck
Koen Van Herck
KHKarin Hardt
Karin Hardt
FTFabian Tibaldi
Fabian Tibaldi
GDGary Dubin
Gary Dubin
PDPierre Van Damme
Pierre Van Damme

8 August 2012 in BMJ
Verified
Journal Article
Open access
PDF file
TBTessa Braeckman
Tessa Braeckman
KHKoen Van Herck
Koen Van Herck
NMNadia Meyer
Nadia Meyer
JPJean-Yves Pirçon
Jean-Yves Pirçon
MSMontse Soriano-Gabarró
Montse Soriano-Gabarró
OGon behalf of the RotaBel Study Group
on behalf of the RotaBel Study Group
Objective To evaluate the effectiveness of rotavirus vaccination among young children in Belgium. Design Prospective case-control study. Setting Random sample of 39 Belgian hospitals, February 2008 to June 2010. Participants 215 children admitted to hospital with rotavirus gastroenteritis confirmed by polymerase chain reaction and 276 age and hospital matched controls. All children were of an eligible age to have received rotavirus vaccination (that is, born after 1 October 2006 and aged ≥14 weeks). Main outcome measure Vaccination status of children admitted to hospital with rotavirus gastroenteritis and matched controls. Results 99 children (48%) admitted with rotavirus gastroenteritis and 244 (91%) controls had received at least one dose of any rotavirus vaccine (P<0.001). The monovalent rotavirus vaccine accounted for 92% (n=594) of all rotavirus vaccine doses. With hospital admission as the outcome, the unadjusted effectiveness of two doses of the monovalent rotavirus vaccine was 90% (95% confidence interval 81% to 95%) overall, 91% (75% to 97%) in children aged 3-11 months, and 90% (76% to 96%) in those aged ≥12 months. The G2P[4] genotype accounted for 52% of cases confirmed by polymerase chain reaction with eligible matched controls. Vaccine effectiveness was 85% (64% to 94%) against G2P[4] and 95% (78% to 99%) against G1P[8]. In 25% of cases confirmed by polymerase chain reaction with eligible matched controls, there was reported co-infection with adenovirus, astrovirus and/or norovirus. Vaccine effectiveness against co-infected cases was 86% (52% to 96%). Effectiveness of at least one dose of any rotavirus vaccine (intention to vaccinate analysis) was 91% (82% to 95%). Conclusions Rotavirus vaccination is effective for the prevention of admission to hospital for rotavirus gastroenteritis among young children in Belgium, despite the high prevalence of G2P[4] and viral co-infection.

10 April 2018 in Helicobacter
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Journal Article
Closed access
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KVKimberly Venneman
Kimberly Venneman
Inge HuybrechtsInge Huybrechts
Inge Huybrechts
MGMarc J. Gunter
Marc J. Gunter
LVLieve Vandendaele
Lieve Vandendaele
RHRolando Herrero
Rolando Herrero
KHKoen Van Herck
Koen Van Herck