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Chronic pain and fatigue in patients with multiple osteochondroma and Ollier disease: A systematic review 

Project leader

Dr. Ariane Kwiet, MD, PhD

Abstract

Multiple osteochondromas (MO) and Ollier disease (OD) are to rare diseases that feature benign tumors in the skeletal bones. Common complications are bone deformity, restricted joint motion, interference with skeletal growth and risk for malign transformation. A large part of the literature focuses on genetics or surgical interventions. Recently, however, some studies suggested that chronic pain and fatigue is a problem in these diseases.

This systematic review has three main goals: a) present existing research on chronic pain and fatigue in MO and OD patients, b) make clinicians aware of current knowledge on fatigue and chronic pain c) identify gaps and topics for future research.   

We conducted a systematic search in the following databases: MEDLINE (Ovid), Embase (Ovid), APA PsycInfo (Ovid), CINAHL (EBSCO), Science Citation Index Expanded (Web of Science). We included studies examining children and/ or adults with either MO or OD and where chronic pain and/ or fatigue is part of the assessment. From the included studies, we will extract information on study background, patients, pain and fatigue (prevalence, type, intensity, duration, treatment and assessment tools). We will also assess study quality and focus on future research targets.  

Results of this review can be used in treatment guidelines and shall be used as a basis for a future study about chronic pain and fatigue in these diagnoses.

Projectleader

Ariane Kwiet 

Senior Consultant / ph.d., Sunnaas Rehabilitation Hospital

Project employees

Trine Bathen, Occupational Therapy Specialist, Sunnaas Rehabilitation Hospital
 
Brede Damann, Social worker, Sunnaas Rehabilitation Hospital

Hilde Strømme, Academic Librarian, Library of Medicine and Science at University of Oslo.

Ethical approvals

Not applicable

Funding

No extern founding.

Time period

Desember 2022 – July 2024 

Hva er TRS?

TRS er et nasjonalt kompetansesenter for sjeldne, medfødte skjelett- og bindevevstilstander, ryggmargsbrokk og dysmeli. Målgruppene er de som har en av diagnosene, pårørende, helsepersonell og andre aktuelle fagpersoner. Senteret er en del av Nasjonal kompetansetjeneste for sjeldne diagnoser og ligger på Sunnaas sykehus på Nesodden utenfor Oslo.
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Last updated 11/28/2023