Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]

<p>Abstract</p> <p>Background</p> <p>The design of a randomized multicenter trial is presented on the effectiveness of a prolonged conservative treatment strategy compared with surgery in patients with persisting intense sciatica (lumbosacral radicular syndrome).</p&...

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Main Authors: Tans Joseph, Eekhof Just AH, Brand Ronald, van der Hout Wilbert B, van Houwelingen Hans C, Peul Wilco C, Thomeer Ralph TWM, Koes Bart W
Format: Article
Language:English
Published: BMC 2005-02-01
Series:BMC Musculoskeletal Disorders
Online Access:http://www.biomedcentral.com/1471-2474/6/8
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spelling doaj-94a7ba54459d4f5cb32958c3875e68a72020-11-25T01:41:36ZengBMCBMC Musculoskeletal Disorders1471-24742005-02-0161810.1186/1471-2474-6-8Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]Tans JosephEekhof Just AHBrand Ronaldvan der Hout Wilbert Bvan Houwelingen Hans CPeul Wilco CThomeer Ralph TWMKoes Bart W<p>Abstract</p> <p>Background</p> <p>The design of a randomized multicenter trial is presented on the effectiveness of a prolonged conservative treatment strategy compared with surgery in patients with persisting intense sciatica (lumbosacral radicular syndrome).</p> <p>Methods/design</p> <p>Patients presenting themselves to their general practitioner with disabling sciatica lasting less than twelve weeks are referred to the neurology outpatient department of one of the participating hospitals. After confirmation of the diagnosis and surgical indication MRI scanning is performed. If a distinct disc herniation is discerned which in addition covers the clinically expected site the patient is eligible for randomization. Depending on the outcome of the randomization scheme the patient will either be submitted to prolonged conservative care or surgery. Surgery will be carried out according to the guidelines and between six and twelve weeks after onset of complaints. The experimental therapy consists of a prolonged conservative treatment under supervision of the general practitioner, which may be followed by surgical intervention in case of persisting or progressive disability. The main primary outcome measure is the disease specific disability of daily functioning. Other primary outcome measures are perceived recovery and intensity of legpain. Secondary outcome measures encompass severity of complaints, quality of life, medical consumption, absenteeism, costs and preference. The main research question will be answered at 12 months after randomization. The total follow-up period covers two years.</p> <p>Discussion</p> <p>Evidence is lacking concerning the optimal treatment of lumbar disc induced sciatica. This pragmatic randomized trial, focusses on the 'timing' of intervention, and will contribute to the decision of the general practictioner and neurologist, regarding referral of patients for surgery.</p> http://www.biomedcentral.com/1471-2474/6/8
collection DOAJ
language English
format Article
sources DOAJ
author Tans Joseph
Eekhof Just AH
Brand Ronald
van der Hout Wilbert B
van Houwelingen Hans C
Peul Wilco C
Thomeer Ralph TWM
Koes Bart W
spellingShingle Tans Joseph
Eekhof Just AH
Brand Ronald
van der Hout Wilbert B
van Houwelingen Hans C
Peul Wilco C
Thomeer Ralph TWM
Koes Bart W
Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
BMC Musculoskeletal Disorders
author_facet Tans Joseph
Eekhof Just AH
Brand Ronald
van der Hout Wilbert B
van Houwelingen Hans C
Peul Wilco C
Thomeer Ralph TWM
Koes Bart W
author_sort Tans Joseph
title Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
title_short Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
title_full Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
title_fullStr Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
title_full_unstemmed Prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [ISRCT 26872154]
title_sort prolonged conservative treatment or 'early' surgery in sciatica caused by a lumbar disc herniation: rationale and design of a randomized trial [isrct 26872154]
publisher BMC
series BMC Musculoskeletal Disorders
issn 1471-2474
publishDate 2005-02-01
description <p>Abstract</p> <p>Background</p> <p>The design of a randomized multicenter trial is presented on the effectiveness of a prolonged conservative treatment strategy compared with surgery in patients with persisting intense sciatica (lumbosacral radicular syndrome).</p> <p>Methods/design</p> <p>Patients presenting themselves to their general practitioner with disabling sciatica lasting less than twelve weeks are referred to the neurology outpatient department of one of the participating hospitals. After confirmation of the diagnosis and surgical indication MRI scanning is performed. If a distinct disc herniation is discerned which in addition covers the clinically expected site the patient is eligible for randomization. Depending on the outcome of the randomization scheme the patient will either be submitted to prolonged conservative care or surgery. Surgery will be carried out according to the guidelines and between six and twelve weeks after onset of complaints. The experimental therapy consists of a prolonged conservative treatment under supervision of the general practitioner, which may be followed by surgical intervention in case of persisting or progressive disability. The main primary outcome measure is the disease specific disability of daily functioning. Other primary outcome measures are perceived recovery and intensity of legpain. Secondary outcome measures encompass severity of complaints, quality of life, medical consumption, absenteeism, costs and preference. The main research question will be answered at 12 months after randomization. The total follow-up period covers two years.</p> <p>Discussion</p> <p>Evidence is lacking concerning the optimal treatment of lumbar disc induced sciatica. This pragmatic randomized trial, focusses on the 'timing' of intervention, and will contribute to the decision of the general practictioner and neurologist, regarding referral of patients for surgery.</p>
url http://www.biomedcentral.com/1471-2474/6/8
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