Lise Hestbæk

Prof. Lise Hestbæk

Nordisk Institut for Kiropraktik og Klinisk Biomekanik, Odense, Syddanmark, Denmark
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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1 April 2003 in European Spine Journal
Verified
Journal Article
Closed access
LHLise Hestbæk
Lise Hestbæk
CLCharlotte Leboeuf-Yde
Charlotte Leboeuf-Yde
CMClaus Manniche
Claus Manniche

1 February 2006 in Spine
Verified
Journal Article
Closed access
LHLise Hestbæk
Lise Hestbæk
CLCharlotte Leboeuf-Yde
Charlotte Leboeuf-Yde
KKKirsten Ohm Kyvik
Kirsten Ohm Kyvik
CMClaus Manniche
Claus Manniche
Prospective study with 8-year follow-up. To describe the evolution of low back pain from adolescence into adulthood. High prevalence rates of low back pain among children and adolescents have been demonstrated in several studies, and it has been theorized that low back pain in childhood may have important consequences for future low back pain. It is important to understand the nature of such a link if effective preventive programs are to be established. Almost 10,000 Danish twins born between 1972 and 1982 were surveyed by means of postal questionnaires in 1994 and again in 2002. The questionnaires dealt with various aspects of general health, including the prevalence of low back pain, classified according to number of days affected (0, 1-7, 8-30, >30). Low back pain in adolescence was found to be a significant risk factor for low back pain in adulthood with odds ratios as high as four. We also demonstrated a dose-response association: the more days with low back pain at baseline, the higher the risk of future low back pain. Twenty-six percent of those with low back pain for more than 30 days during the baseline year also had more than 30 days with low back pain during the follow-up year. This was true for only 9% of the rest of the sample. Our study clearly demonstrates correlations between low back pain in childhood/adolescence and low back pain in adulthood. This should lead to a change in focus from the adult to the young population in relation to research, prevention, and treatment.

1 June 2016 in Brazilian Journal of Physical Therapy
Verified
Journal Article
Open access
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SKSteve J. Kamper
Steve J. Kamper
NHNicholas Henschke
Nicholas Henschke
LHLise Hestbæk
Lise Hestbæk
KDKate M. Dunn
Kate M. Dunn
CWChristopher M. Williams
Christopher M. Williams
Key words: children; adolescents; musculoskeletal pain; burden; epidemiology

1 October 2013 in Best Practice & Research Clinical Rheumatology
Verified
Journal Article
Closed access
KDKate M. Dunn
Kate M. Dunn
LHLise Hestbæk
Lise Hestbæk
JCJ. David Cassidy
J. David Cassidy

1 July 2006 in Journal of Manipulative and Physiological Therapeutics
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Journal Article
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MSMette Jensen Stochkendahl
Mette Jensen Stochkendahl
HCHenrik Wulff Christensen
Henrik Wulff Christensen
JHJan Hartvigsen
Jan Hartvigsen
WVWerner Vach
Werner Vach
MHMitchell Haas
Mitchell Haas
GBGert Bronfort
Gert Bronfort
Poor reproducibility of spinal palpation has been reported in previously published literature, and authors of recent reviews have posted criticism on study quality. This article critically analyzes the literature pertaining to the inter- and intraobserver reproducibility of spinal palpation to investigate the consistency of study results and assess the level of evidence for reproducibility. Systematic review and meta-analysis were performed on relevant literature published from 1965 to 2005, identified using the electronic databases MEDLINE, MANTIS, and CINAHL and checking of reference lists. Descriptive data from included articles were extracted independently by 2 reviewers. A 6-point scale was constructed to assess the methodological quality of original studies. A meta-analysis was conducted among the high-quality studies to investigate the consistency of data, separately on motion palpation, static palpation, osseous pain, soft tissue pain, soft tissue changes, and global assessment. A standardized method was used to determine the level of evidence. The quality score of 48 included studies ranged from 0% to 100%. There was strong evidence that the interobserver reproducibility of osseous and soft tissue pain is clinically acceptable (kappa > or = 0.4) and that intraobserver reproducibility of soft tissue pain and global assessment are clinically acceptable. Other spinal procedures are either not reproducible or the evidence is conflicting or preliminary.

16 March 2006 in BMC Musculoskeletal Disorders
Verified
Journal Article
Open access
PDF file
LHLise Hestbæk
Lise Hestbæk
CLCharlotte Leboeuf-Yde
Charlotte Leboeuf-Yde
KKKirsten O Kyvik
Kirsten O Kyvik
Background: It has previously been shown that low back pain (LBP) often presents already in the teenage years and that previous LBP predicts future LBP. It is also well documented that there is a large degree of comorbidity associated with LBP, both in adolescents and adults. The objective of this study is to gain a deeper insight into the etiology of low back pain and to possibly develop a tool for early identification of high-risk groups. This is done by investigating whether different types of morbidity in adolescence are associated with LBP in adulthood. Methods: Almost 10,000 Danish twins born between 1972 and 1982 were surveyed by means of postal questionnaires in 1994 and again in 2002. The questionnaires dealt with various aspects of general health, including the prevalence of LBP, classified according to number of days affected during the previous year (0, 1–7, 8–30, >30). The predictor variables used in this study were LBP, headache, asthma and atopic disease at baseline; the outcome variable was persistent LBP (>30 days during the past year) at follow-up. Associations between morbidity in 1994 and LBP in 2002 were investigated. Results: LBP, headache and asthma in adolescence were positively associated with future LBP. There was no association between atopic disease and future LBP. Individuals with persistent LBP at baseline had an odds ratio of 3.5 (2.8–4.5) for future LBP, while the odds ratio for those with persistent LBP, persistent headache and asthma was 4.5 (2.5–8.1). There was a large degree of clustering of these disorders, but atopic disease was not part of this pattern. Conclusion: Young people from 12 to 22 years of age with persistent LBP during the previous year have an odds ratio of 3.5 persistent LBP eight years later. Both headache and asthma are also positively associated with future LBP and there is a large clustering of LBP, headache and asthma in adolescence.