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Course of disability reduction during a pain rehabilitation
program: a prospective clinical study
Franka P.C. Waterschoot
a
, Pieter U. Dijkstra
a,b
, Jan H.B. Geertzen
a
and
Michiel F. Reneman
a
The aim of this study was to analyze the course of reduction
of disability during a pain rehabilitation program (PRP) and
factors influencing this course. A prospective cohort study
was carried out. All patients with chronic musculoskeletal
pain treated in a PRP between March 2010 and December
2010 were eligible for this study. All patients were treated at
a University-based rehabilitation center and received an
outpatient multidisciplinary PRP. Main outcome measures,
Pain Disability Index (PDI), and average pain measured with
a numeric rating scale were measured every 2 weeks during
the PRP. To analyze the course of disability, a linear mixed-
effect model was applied. One hundred and twenty-eight
patients participated in the study, of whom 20% dropped out
during the PRP. Initial PDI (β = 0.8), treatment week
(β = - 0.2), treatment week squared (β = 0.03), average pain
(β = 2.3), and interaction between initial PDI and treatment
week (β = - 0.02) influenced the course of disability during
PRP. Disability reduces during the PRP. Initial PDI, treatment
week, average pain, and interaction between initial PDI and
treatment week influence the course of disability reduction
during the PRP. These results could aid in predicting the
required duration of a PRP at the start. International Journal
of Rehabilitation Research 00:000–000 © 2014
Wolters Kluwer Health | Lippincott Williams & Wilkins.
International Journal of Rehabilitation Research 2014, 00:000–000
Keywords: chronic pain, disability, Pain Disability Index, patient care team,
rehabilitation
a
Department of Rehabilitation Medicine, Centre for Rehabilitation and
b
Department of Oral and Maxillofacial Surgery, University Medical Centre
Groningen, University of Groningen, Groningen, The Netherlands
Correspondence to Franka P.C. Waterschoot, BSH, Department of Rehabilitation
Medicine, Center for Rehabilitation, University Medical Center Groningen,
University of Groningen, PO Box 30002, 9750 RA Haren, Groningen,
The Netherlands
Tel: + 31 505 338 444; fax: + 31 505 338 570;
e-mail: f.p.c.waterschoot@umcg.nl
Received 21 February 2014 Accepted 26 August 2014
Introduction
On the basis of pre and post measurements, it is known
that pain rehabilitation programs (PRPs) are effective in
disability reduction in patients with chronic musculoske-
letal pain (CMP) (Guzman et al., 2001; Jensen et al., 2001;
McCracken and Turk, 2002; Skouen et al., 2002; Gatchel
and Okifuji, 2006; Smeets et al., 2006; Scascighini et al.,
2008). However, the course of disability reduction is
unknown. Understanding the course of disability reduc-
tion could aid in determining the optimum duration of
PRPs. This understanding would benefit patients, clin-
icians, insurance companies, and healthcare providers
because it prevents overtreatment or undertreatment and
contributes toward better use of (public) recourses.
A wide diversity of content, composition, and duration of
PRPs exist (Guzman et al., 2001; Scascighini et al., 2008).
In one systematic review, differences in duration were
unrelated to differences in outcomes (Scascighini et al.,
2008). However, in another review it was reported that
multidisciplinary PRP of more than 100 h was superior to
monodisciplinary treatment, and that multidisciplinary
PRP of less than 30 h was not superior to mono-
disciplinary treatment. Although the authors focused on
the content of different PRPs and the review was
designed to assess the effect of PRP, they concluded
that PRPs of more than 100 h were more effective.
The conclusions of these reviews were used to establish
guidelines and clinical practice (Airaksinen et al., 2006;
Van Hooff et al., 2010). However, these conclusions were
based only on pre–post assessments. To our knowledge,
no studies have analyzed the course of disability reduc-
tion during the programs to establish the optimum
duration of a PRP. In addition, it is unknown whether the
improvements gained with intensive PRPs are worth the
expenses (Guzman et al., 2001). Theoretically, if 90% of
the improvements are observed in the first half of the
PRP, it may be debated whether these 100 h or more, as
proposed by Guzman et al. (2001), are needed.
Because no previous research is available into this spe-
cific aspect of PRPs, we hypothesized that there would
be several possible courses of reduction of disability
(Fig. 1). Line A assumes that the course of disability has a
steeper slope at the end of the PRP. This implies that
disability decreases most in the last part of the PRP. In
contrast, line B assumes a steeper slope at the first half of
the PRP. This implies that disability decreases most in
the first part of the PRP. Line C implies a linear decrease
of disability, and an alternating pattern of decrease and
increase during the PRP is hypothesized in line D.
The aim of this study was to analyze the course of
reduction of disability during PRP and to analyze factors
influencing this course.
Original article 1
0342-5282 © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins DOI: 10.1097/MRR.0000000000000087