JORGE H. VILLAFAÑE, PT, PhD1 • JOSHUA A. CLELAND, PT, PhD2 • CÉSAR FERNÁNDEZ-DE-LAS-PEÑAS, PT, PhD3
T
placebo intervention in individuals with carpo-
receiving the placebo intervention at the end of the
metacarpal (CMC) joint osteoarthritis (OA).
intervention, as well as at 1 and 2 months after the he carpometacarpal
TTBACKGROUND: Recent studies have reported intervention (P<.001; all group differences greater
the outcomes of exercise, joint mobilization, and
(CMC) joint of the thumb
than 3.0 cm, which is greater than the minimal
neural mobilization interventions used in isolation clinically important difference of 2.0 cm). A signifi- plays a vital role in the
in patients with CMC joint OA. However, it is not cant group-by-time interaction (F = 3.19, P = .025) function of the hand.
known if using a combination of these interven- was found for pressure pain threshold over the
tions as a multimodal approach to treatment The first CMC joint is frequently
hamate bone immediately after the intervention;
would further improve outcomes in this patient however, the interaction was no longer significant affected by osteoarthritis (OA), a
population. at 1 and 2 months postintervention.
degenerative condition resulting in dete-
TTMETHODS: Sixty patients, 90% female (mean TTCONCLUSION: This clinical trial provides rioration of the joint surfaces and even-
SD age, 82 6 years), with CMC joint OA evidence that a combination of joint mobiliza-
were randomly assigned to receive a multimodal tual bone remodeling.2 The consequence
tion, neural mobilization, and exercise is more
manual treatment approach that included joint beneficial in treating pain than a sham interven-
of CMC joint OA is severe pain, leading
mobilization, neural mobilization, and exercise, or tion in patients with CMC joint OA. However, the to considerable limitations in function
a sham intervention, for 12 sessions over 4 weeks. treatment approach has limited value in improving and disability, and a substantial societal
The primary outcome measure was pain. Second- pressure pain thresholds, as well as pinch and grip burden.2,15,42,44 Patients with CMC joint
ary outcome measures included pressure pain strength. Future studies should include several OA represent the cohort of individu-
threshold over the first CMC joint, scaphoid, and therapists, a measure of function, and long-term
hamate, as well as pinch and strength measure- als with upper extremity arthritis most
outcomes. Trial registration: Current Controlled
ments. All outcome measures were collected at Trials ISRCTN37143779.
likely to undergo surgical intervention. 3
However, previous studies examining the
TTLEVEL OF EVIDENCE: Therapy, level 1b.
baseline, immediately following the intervention,
and at 1 and 2 months following the end of the in- effectiveness of surgical intervention have
J Orthop Sports Phys Ther 2013;43(4):204-213.
tervention. Mixed-model analyses of variance were reported varied levels of benefits in terms
Epub 13 March 2013. doi:10.2519/jospt.2013.4524
used to examine the effects of the interventions on
TTKEY WORDS: arthritis, CMC, joint mobilization,
of pain reduction and improved function,
each outcome, with group as the between-subject
variable and time as the within-subject variable. neural mobilization and have demonstrated an adverse event
rate of between 10% and 22%, depend-
1
Department of Physical Therapy. Residenza Sanitaria Assistenziale “A. Maritano,” Sangano, Italy; Private practice, Turin, Italy. 2Department of Physical Therapy, Franklin Pierce
University, Concord, NH; Rehabilitation Services, Concord Hospital, Concord, NH; Manual Therapy Fellowship Program, Regis University, Denver, CO. 3Department of Physical
Therapy, Occupational Therapy, Rehabilitation and Physical Medicine, Universidad Rey Juan Carlos, Alcorcón, Madrid, Spain; Esthesiology Laboratory, Universidad Rey Juan
Carlos, Alcorcón, Madrid, Spain. This work was supported by the personal funds of Jorge Hugo Villafañe. The authors certify that they have no affiliations with or financial
involvement in any organization or entity with a direct financial interest in the subject matter or materials discussed in the manuscript. The study protocol was approved by
the Local Ethical Committee in Azienda Sanitaria Locale 3, Collegno, Italy. Address correspondence to Dr Jorge Hugo Villafañe, Regione Generala 11/16, Piossasco, Italy 10045.
E-mail: mail@villafane.it t Copyright ©2013 Journal of Orthopaedic & Sports Physical Therapy
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to a placebo intervention demonstrated e conducted a double-blind,
greater improvements in PPT measured randomized controlled trial. In- Outcome Measures
over the first CMC joint and greater im- formed consent was obtained Current Pain The primary outcome mea-
provements in pinch strength in the in- from all participants, and the study pro- sure was pain intensity of the first CMC
tervention group. However, all these tocol was conducted according to the joint, which was assessed with a visual
studies investigated the effects of a single Declaration of Helsinki. The protocol analog scale (VAS). The VAS is a 10-cm
intervention approach, which does not (number 93571/c) was approved by the line, anchored with 0 at one end, repre-
represent typical clinical practice in the Local Ethical Committee in Azienda senting no pain, and 10 at the other end,
management of these patients. Joint mo- Sanitaria Locale 3, Collegno, Italy (nurs- representing the worst pain imaginable. 9
bilization techniques, traction, and glide ing home). The study was registered Pain was assessed by having the partici-
are often used in this population to stretch after completion at the Current Con- pant perform a key pinch between the
the joint capsule to improve physiological trolled Trials trial-registration website thumb and the index finger. The VAS was
accessory motions,34 to improve limited (ISRCTN37143779). selected as the primary outcome mea-
range of motion, and to reduce pain.28,36 sure, based on its ability to detect changes
Hand exercises for CMC joint OA are Participants (minimal clinically important difference,
aimed at maximizing pain-free range of Sixty participants, 65 to 90 years of age, 2.0 cm).18,19
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eventy (n = 70) consecutive indi-
viduals with CMC joint OA were
screened for eligibility criteria. Experimental Group Placebo Group
Sixty patients (mean SD age, 82 6 (n = 30) (n = 30) P Value
years; 90% female) satisfied all eligibility Age, y 82 2 83 1 .61
criteria, agreed to participate, and were Gender (female/male), n 27/3 24/6 .47
randomized to the control (n = 30) or Pain (visual analog scale, 0-10), cm 5.0 0.3 5.0 0.2 .89
sons for ineligibility were bilateral pain Lateral epicondyle, affected side 5.9 0.3 5.5 0.4 .45
symptoms (n = 5), no confirmation of the Lateral epicondyle, nonaffected side 5.1 0.3 5.1 0.4 .87
diagnosis with radiographs (n = 3), and Carpometacarpal joint, affected side 3.3 0.2 3.4 0.2 .64
the concurrent presence of De Quervain Carpometacarpal joint, nonaffected side 3.2 0.2 3.3 0.2 .91
tenosynovitis (n = 2). FIGURE 4 provides Hamate bone, affected side 5.5 0.4 5.5 0.3 .96
Hamate bone, nonaffected side 5.4 0.4 5.5 0.3 .78
a flow diagram of subject recruitment
Tip pinch and grip strength, kg
and retention through the study. All
Tip pinch, affected side 2.3 0.2 2.3 0.3 .99
subjects were right-hand dominant and
Tip pinch, nonaffected side 2.3 0.2 2.1 0.2 .56
were affected on the right side. Baseline
Grip strength, affected side 10.6 1.0 10.7 1.2 .97
features of both groups were similar for
Grip strength, nonaffected side 10.3 1.1 10.1 1.6 .91
all variables (TABLE 2). No adverse effects
were detected during or after the appli- Abbreviation: PPT, pressure pain threshold.
*Values are mean SD with the exception of gender.
cation of the treatment, and none of the
subjects started drug therapy during the
study. Pressure Pain Thresholds P = .15) or side (F = 1.21, P = .28).
The ICCs for intraexaminer reliability of For PPTs measured over the hamate
First CMC Joint Pain Intensity PPT measurements ranged from 0.84 to bone, the 2-by-2-by-4 ANOVA revealed
The 2-by-4 mixed-model ANOVA in- 0.92 for the affected side and from 0.84 no significant group-by-time-by-side (F
dicated a significant group-by-time in- to 0.92 for the unaffected side. The SEMs = 1.36, P = .25), side-by-time (F = 3.19,
teraction (F = 47.58, P<.001) for pain ranged from 0.51 to 0.65 kg/cm2 for both P = .02), or group-by-side (F = 0.32, P =
intensity. Post hoc analysis indicated sides. .57) interaction. There was a significant
that the patients with thumb CMC joint For PPTs measured over the lateral group-by-time interaction (F = 3.19, P
OA receiving the multimodal interven- epicondyle, there was no significant = .025), with the patients receiving the
tion experienced a significantly greater group-by-time-by-side (F = 0.75, P = .5), experimental protocol exhibiting greater
reduction in pain compared to those group-by-time (F = 1.46, P = .23), side- PPT over the hamate bone, as compared
receiving the placebo intervention im- by-time (F = 0.60, P = .62), or group-by- to those receiving the placebo interven-
mediately postintervention (experimen- side (F = 0.55, P = .82) interaction. There tion, immediately after the intervention
tal group mean, 3.7; 95% CI: 2.4, 3.8; was also no significant main effect for (P<.005) but not at the 1- and 2-month
placebo group mean, 0.3; 95% CI: 0.0, time (F = 1.81, P = .15). There was a sig- follow-ups (TABLE 3).
0.3; difference between groups, 3.4; 95% nificant main effect for side (F = 14.40,
CI: –4.6, –3.2), as well as at the 1-month P<.001), with higher PPT measured over Pinch and Grip Strength
follow-up (experimental group mean, the lateral epicondyle of the affected The ICCs for intraexaminer reliability
3.7; 95% CI: 2.8, 4.1; placebo group hand as compared to the nonaffected of measurements of tip pinch and grip
mean, 0.3; 95% CI: 0.2, 0.8; difference hand (TABLE 3). strength were 0.81 and 0.72 for the affect-
between groups, 3.4; 95% CI: –4.7, –3.3) For PPTs measured over the first CMC ed arm and 0.81 and 0.73 for the unaf-
and 2-month follow-up (experimental joint, the 2-by-2-by-4 ANOVA revealed fected side, respectively. For tip pinch and
group mean, 3.7; 95% CI: 2.9, 4.2; pla- no significant group-by-time-by-side grip strength, the SEMs were 0.75 kg and
cebo group mean, 0.3; 95% CI: 0.2, 0.9; (F = 0.44, P = .72), group-by-time (F = 4.02 kg in the affected arm, respectively,
difference between groups, 3.4; 95% CI: 1.1, P = .35), side-by-time (F = 1.10, P = and 0.51 kg and 4.47 kg in the unaffected
–4.8, –3.3) periods (all, P<.001) (TABLE 3). .35), or group-by-side (F = 0.21, P = .65) side, respectively.
Between-group effect sizes were large at interaction (TABLE 3). There was also no For tip pinch strength, the 2-by-2-by-4
all follow-up periods (d>1.5). significant main effect for time (F = 1.79, ANOVA revealed no significant group-
journal of orthopaedic & sports physical therapy | volume 43 | number 4 | april 2013 | 209
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= 0.80, P = .64) interaction. There were his randomized controlled tri- the reported minimal clinically impor-
also no significant main effects for time (F al examined the effects of joint mo- tant difference of 2.0 cm.18,19 We believe
= 0.8, P = .49) or side (F = 0.05, P = .81). bilization, neural mobilization, and that this provides evidence to support
For grip strength, the 2-by-2-by-4 exercise on a patient population with the use of this multimodal approach in
ANOVA revealed no significant group- CMC joint OA at short-term follow-up. patients with CMC joint OA.
by-time-by-side (F = 1.2, P = .31), group- The results demonstrated that patients In contrast to the differences between
by-time (F = 0.57, P = .64), side-by-time receiving a multimodal intervention of groups for pain, there was no difference
(F = 0.85, P = .47), or group-by-side (F = manual therapy and exercise exhibited between groups for PPT after the inter-
0.66, P = .58) interaction, and no main ef- significantly greater improvements in vention, except when measured over the
fects for time (F = 0.27, P = .85) and side pain compared to those who received a hamate immediately after treatment.
(F = 0.46, P = .5) (TABLE 4). placebo intervention. It is interesting to The current study was powered to detect
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changes in pain, as measured by the VAS, between sensory and motor outcomes are often included as an integral part of
and not PPT. A larger sample size might are expected in this population. Consid- the rehabilitation program.16,17
have detected significant changes in PPT ering the above, the current treatment Despite the fact that patients in the
between groups. Previous studies exam- approach provides little value in inducing experimental group performed exercises
ining the effects of either joint mobiliza- mechanical pain hypoalgesia associated to improve pinch and grip strength for 4
tion49-51 or nerve mobilization49,51 in this with an increase in PPT. Similarly, with- weeks, no changes were identified. These
same population have found a difference out the inclusion of a healthy group, we findings are consistent with the results of
between groups for PPT measurements. cannot determine whether PPTs found Rogers and Wilder,37 who used the same
However, in these studies, the differences in our sample of patients were normal. exercise program in this population. In
in PPT did not exceed the SEM and thus The presence of normal PPTs would also contrast, the authors of a recent review46
were within measurement error and likely explain the lack of effect, as no improve- concluded that the current literature
not clinically meaningful. Our findings are ment could have been made. Future stud- supports the use of orthoses, exercises,
similar to those of a study performed in ies are required to determine the presence application of heat, and joint protec-
individuals with carpal tunnel syndrome, of pressure pain sensitivity in this patient tion education combined with adaptive
in which patients who received neural population. It is possible that if the patient equipment to improve grip strength and
mobilization did not exhibit changes in had received manual therapy directed at function in patients with OA of the hand.
PPT different from those receiving a sham the cervical spine, a change in PPT might Discrepancies between exercise programs
intervention.6 However, as the authors re- have been produced. Numerous studies could be related to the fact that not all reg-
ported, this might have been the result of have shown that interventions directed imens are developed based on a clinical
differing patient expectations, which were to the cervical spine exert a mechanical and biomechanical analysis of the pathol-
not measured in the current study.6 hypoalgesic effect by increasing PPT.20,21,31 ogy.47 Future studies should investigate
We did not observe differences in PPT The increase in PPT over the hamate on which exercise regimens are the most ap-
values between hands. These findings are the affected side immediately postinter- propriate for reducing pain and improv-
in agreement with emerging evidence vention is consistent with the results of ing function in patients with CMC joint
suggesting that OA-related pain cannot Moss et al,33 who showed that joint mo- OA. It should be noted that in our popula-
be attributed exclusively to local joint bilization of the tibia or the femur for 9 tion, despite the pain related to the CMC
nociceptors (peripheral sensitization minutes in patients with knee OA had an joint, there were no apparent strength
processes), because central sensitization immediate, local hypoalgesic effect. These deficits based on the similar strength val-
is also present. Therefore, discrepancies techniques are frequently performed and ues between the affected and nonaffected
journal of orthopaedic & sports physical therapy | volume 43 | number 4 | april 2013 | 211
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the treatment of carpal tunnel syndrome. J Orthop
be stimulated by joint mobilization.5,56 his study provides evidence
Sports Phys Ther. 2009;39:709-723. http://dx.doi.
It has also been shown that with arthri- that a multimodal intervention con- org/10.2519/jospt.2009.3117
tis, mechanical loading of the involved sisting of joint mobilization, neural 7. Bialosky JE, Bishop MD, Robinson ME, Zeppieri G,
tissues resulted in smaller amounts of mobilization, and exercise is beneficial to Jr., George SZ. Spinal manipulative therapy has
an immediate effect on thermal pain sensitivity
substance P released from the dorsal reduce pain in patients with CMC joint
in people with low back pain: a randomized con-
root ganglia and spinal cord, at least OA. However, the treatment approach trolled trial. Phys Ther. 2009;89:1292-1303. http://
in the rat model.32 The reason patients’ did not produce change in PPTs or pinch dx.doi.org/10.2522/ptj.20090058
perception of pain was significantly bet- and grip strength. t 8. Bialosky JE, George SZ, Bishop MD. How spinal
manipulative therapy works: why ask why? J Or-
ter but the PPTs were not better requires
thop Sports Phys Ther. 2008;38:293-295. http://
further elaboration. As mentioned by KEY POINTS dx.doi.org/10.2519/jospt.2008.0118
Bialosky et al,6 this might be directly FINDINGS: The application of a multi- 9. Bijur PE, Silver W, Gallagher EJ. Reliability of the vi-
related to patient expectations, and the modal manual therapy intervention of sual analog scale for measurement of acute pain.
Acad Emerg Med. 2001;8:1153-1157.
treating therapist’s attitude could have joint mobilization, neural mobilization,
10. Bjordal JM, Ljunggren AE, Klovning A, Slørdal L.
impacted the outcomes.48 It is also pos- and exercise is beneficial to reduce Non-steroidal anti-inflammatory drugs, including
sible that psychosocial issues may be as- pain in patients with CMC joint OA. cyclo-oxygenase-2 inhibitors, in osteoarthritic knee
sociated with differing outcomes of pain No changes in PPT and motor function pain: meta-analysis of randomised placebo con-
trolled trials. BMJ. 2004;329:1317. http://dx.doi.
responses. A recent clinical trial involving were observed.
org/10.1136/bmj.38273.626655.63
patients with low back pain showed that IMPLICATIONS: Physical therapists should 11. Butler DS. The Neurodynamic Techniques. Ad-
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with the pain response.7 However, these the management of CMC joint OA–re- 12. Butler DS, Jones MA. Mobilisation of the Nervous
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13. Çelik D, Atalar AC, Şahinkaya S, Demirhan M. [The
rather than PPTs to report the pain re- CAUTION: We only assessed short-term value of intermittent ultrasound treatment in sub-
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delta fiber–mediated pain compared to ter function.
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