Berit Schiøttz-Christensen

Prof. Berit Schiøttz-Christensen

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

View All Publications
1 March 2003 in Acta Radiologica
Verified
Journal Article
Closed access
KPK. Bocker Puhakka
K. Bocker Puhakka
AJA. G. Jurik
A. G. Jurik
NEN. Egund
N. Egund
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
KSK. Stengaard-Pedersen
K. Stengaard-Pedersen
JCJ. VallO Christiansen
J. VallO Christiansen
International academic publisher with offices worldwide. Publishing more than 2,100 journals, over 4,000 new books each year, with a books backlist in excess of 60,000 specialist titles. We are one of the world’s leading publishers of scholarly journals, books, eBooks, textbooks and reference works

18 May 2017 in European Spine Journal
Verified
Journal Article
Closed access
PDF file
PKPer Kjaer
Per Kjaer
AKAlice Kongsted
Alice Kongsted
JHJan Hartvigsen
Jan Hartvigsen
AIAlexander Isenberg-Jørgensen
Alexander Isenberg-Jørgensen
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
TPTina Myung Povlsen
Tina Myung Povlsen

1 June 1999 in Family Practice
Verified
Journal Article
Open access
PDF file
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
GNGunnar Lauge Nielsen
Gunnar Lauge Nielsen
VHVivian Kjær Hansen
Vivian Kjær Hansen
TSTorben Schødt
Torben Schødt
Henrik Toft SørensenHenrik Toft Sørensen
Henrik Toft Sørensen
FOFrede Olesen
Frede Olesen
Objective. We aimed to examine the prognosis of acute low back pain (LBP) in patients in general practice and to identify prognostic factors associated with the long-term prognosis based on information immediately available to the GP. Method. We conducted a prospective cohort study in general practice in Denmark. The patients were those aged 18–60 years consulting their GP due to an episode of LBP lasting less than 2 weeks. The GPs collected data regarding 34 exposure variables, including their global assessment of the likelihood of chronic LBP. Outcome variables were collected from the patients after 1, 6 and 12 months. The outcome measures were days on sick leave, and functional or complete recovery from LBP. Results. In total, 503 (96%) patients were followed during the whole study period. Fifty per cent of the patients on sick leave returned to work within 8 days; after 1 year, only 2% remained on sick leave. At the 1-year follow-up, 45% of the patients continued to complain of LBP. Logistic regression analyses showed that the factors most significantly associated with poor long-term LBP outcome were (i) severity of LBP at inclusion, (ii) assessments by the GP of susceptibility to develop chronic LBP and (iii) a history of LBP having caused previous sick leave. Conclusions. LBP in general practice has a good prognosis with regard to sick leave, but a high proportion of patients continue to complain of LBP. We were not able to identify objective measures that strongly predict the prognosis of the individual LBP patient. The overall assessment by the GPs seems to be the most important predictor associated with the long-term outcome.

1 November 2017 in Clinical Epidemiology
Verified
Journal Article
Open access
PDF file
EIElse Helene Ibfelt
Else Helene Ibfelt
JSJan Sørensen
Jan Sørensen
DJDorte V. Jensen
Dorte V. Jensen
LDLene Dreyer
Lene Dreyer
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
MHMerete Lund Hetland
Merete Lund Hetland

Objectives:
In Denmark, patients with rheumatoid arthritis (RA) are registered in the nationwide clinical DANBIO quality register and the Danish National Patient Registry (DNPR). The aim was to study the validity of the RA diagnosis and to estimate the completeness of relevant RA cases in each registry. Study design and setting: Patients registered for the first time in 2011 with a diagnosis of RA were identified in DANBIO and DNPR in January 2013. For DNPR, filters were applied to reduce false-positive cases. The diagnosis was verified by a review of patient records. We calculated the positive predictive values (PPVs) of the RA diagnosis registrations in DANBIO and DNPR, and estimated the registry completeness of relevant RA cases for both DANBIO and DNPR. Updated data from 2011 to 2015 from DANBIO were retrieved to identify patients with delayed registration, and the registry completeness and PPV was recalculated. Results: We identified 1,678 unique patients in DANBIO or in DNPR. The PPV (2013 dataset) was 92% in DANBIO and 79% in DNPR. PPV for DANBIO on the 2015 update was 96%. The registry completeness of relevant RA cases was 43% in DANBIO, increasing to 91% in the 2015 update and 90% in DNPR. Conclusion: DANBIO held a high proportion of true RA cases (96%) and was found to be superior to the DNPR (79%) with regard to the validity of the diagnosis. Both registries were estimated to have a high completeness of RA cases treated in hospital care (~90%).

1 August 2015 in Clinical Epidemiology
Verified
Journal Article
Open access
PDF file
PKPeter Kent
Peter Kent
AKAlice Kongsted
Alice Kongsted
TJTue Secher Jensen
Tue Secher Jensen
HAHanne B Albert
Hanne B Albert
CMClaus Manniche
Claus Manniche
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
Background: Large-scale clinical registries are increasingly recognized as important resources for quality assurance and research to inform clinical decision-making and health policy. We established a clinical registry (SpineData) in a conservative care setting where more than 10,000 new cases of spinal pain are assessed each year. This paper describes the SpineData registry, summarizes the characteristics of its clinical population and data, and signals the availability of these data as a resource for collaborative research projects. Methods: The SpineData registry is an Internet-based system that captures patient data electronically at the point of clinical contact. The setting is the government-funded Medical Department of the Spine Centre of Southern Denmark, Hospital Lillebaelt, where patients receive a multidisciplinary assessment of their chronic spinal pain. Results: Started in 2011, the database by early 2015 contained information on more than 36,300 baseline episodes of patient care, plus the available 6-month and 12-month follow-up data for these episodes. The baseline questionnaire completion rate has been 93%; 79% of people were presenting with low back pain as their main complaint, 6% with mid-back pain, and 15% with neck pain. Collectively, across the body regions and measurement time points, there are approximately 1,980 patient-related variables in the database across a broad range of biopsychosocial factors. To date, 36 research projects have used data from the SpineData registry, including collaborations with researchers from Denmark, Australia, the United Kingdom, and Brazil. Conclusion: We described the aims, development, structure, and content of the SpineData registry, and what is known about any attrition bias and cluster effects in the data. For epidemiology research, these data can be linked, at an individual patient level, to the Danish population-based registries and the national spinal surgery registry. SpineData also has potential for the conduct of cohort multiple randomized controlled trials. Collaborations with other researchers are welcome.

16 September 2003 in Rheumatology
Verified
Journal Article
Open access
PDF file
KPK. B. Puhakka
K. B. Puhakka
AJA. G. Jurik
A. G. Jurik
BSBerit Schiøttz-Christensen
Berit Schiøttz-Christensen
GHG. V. O. Hansen
G. V. O. Hansen
NEN. Egund
N. Egund
KSK. Stengaard-Pedersen
K. Stengaard-Pedersen
Objective: To compare a new MRI scoring system of the sacroiliac joints (SIJs) in early spondylarthropathy (SpA) with clinical and laboratory parameters. Methods: Forty-one patients (24 males, 17 females) with a median age of 26 yr and a median duration of inflammatory low back pain of 19 months were included. They all fulfilled the ESSG-criteria for SpA. The patients were examined by MRI of the SIJs using a new scoring system. Clinical examinations, biochemical tests, functional score (BASFI), and pain score (BASDAI) were also performed. Results: 95% of the patients had inflammation and/or destructive bone changes of the SIJs at MRI. No correlation was found between MRI pathology and clinical findings. MRI demonstrated significantly greater severity of both inflammation and destruction of the SIJs in HLA B27 positive patients than in the HLA B27 negative patients. Conclusions: In patients with early SpA, MRI was able to detect inflammatory and destructive changes of the SIJs, but the changes were not associated to clinical findings. Our results suggest a role of MRI in the detection of early-stage sacroiliitis.