ACE Report Cover
Dilatation combined with steroid injections equivalent to steroid in adhesive capsulitis
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Language
Download Download Download
Download
Cite this Report Cite this Report Cite this Report
Cite
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favorites
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Language
Download Download Download
Download
Cite this Report Cite this Report Cite this Report
Cite
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favorites
SHOULDER & ELBOW
Dilatation combined with steroid injections equivalent to steroid in adhesive capsulitis .

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2013;1(2):149 BMC Musculoskelet Disord. 2008 Apr 19;9:53.

76 patients diagnosed with adhesive capsulitis, having predominantly 1 shoulder pain for >3 months in the last 2 years, were randomized to undergo hydrodilatation with corticosteroid injection or just corticosteroid intra-articular injection. This study aimed to compare the clinical results between techniques. At 6 weeks, no major significant between-group differences in most of the outcome measures were recorded. There was a similar degree of improvement from baseline in both of the treatment groups, hence questioning the role of hydrodilation in management of adhesive capsulitis.


Publication Funding Details +
Funding:
Non-Industry funded
Sponsor:
Research Council of Norway, the University of Oslo and Ulleval University Hospital
Conflicts:
None disclosed

Risk of Bias

6/10

Reporting Criteria

17/21

Fragility Index

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Yes = 1

Uncertain = 0.5

Not Relevant = 0

No = 0

The Reporting Criteria Assessment evaluates the transparency with which authors report the methodological and trial characteristics of the trial within the publication. The assessment is divided into five categories which are presented below.

2/4

Randomization

2/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

Therapy Description

5/5

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

The Fragility Index is a tool that aids in the interpretation of significant findings, providing a measure of strength for a result. The Fragility Index represents the number of consecutive events that need to be added to a dichotomous outcome to make the finding no longer significant. A small number represents a weaker finding and a large number represents a stronger finding.

Why was this study needed now?

Evidence has suggested that the etiology of patients with adhesive capsulitis may result from the contractions of the shoulder and intraarticular adhesions. Hydrodilatation of the glenohumeral joint has thus been advocated for improvement of shoulder pain and range of motion in these patients. However, evidence remains inconclusive due to methodological issues. This study investigated the effect of hydrodilatation on the overall treatment effects of a combined dilatation and steroid injection procedure.

What was the principal research question?

Are there clinical differences between patients receiving dilatation (DIL) with a corticosteroid and patients receiving Injection (INJ) of a corticosteroid in the treatment of adhesive capsulitis?

Study Characteristics +
Population:
76 patients (18-70) with diagnosis of adhesive capsulitis, pain in one shoulder lasting >3 months, and limited passive movement in glenohumeral joint >30 degrees (versus opposite shoulder) in 2 of: forward flexion, abduction, external rotation.
Intervention:
Dilatation (DIL): Injection was comprised of: 4 ml of contrast dye, 2 ml triamcinolone acetonide, 4 ml local anesthetic and 10 ml physiological saline. Injection into the joint was performed slowly, and was paused upon resistance before continuing. This technique facilitated gradual joint distension and rupture. 3 injections were administered at two-week intervals (n=39; Mean age: 52+/-7; 26 females)
Comparison:
Injection (INJ): Following location of desired position (with fluoroscopy), 3-4 mL of contrast dye was injected, followed by 2 mL triamcinolone acetonide, and 3-4 mL of local anesthetic (bupivacaine, hydrochloride, Marcain 5mg/mL, Astra-Zeneca). Patients were administered 3 injections at two-week intervals. (n=37; Mean age: 51+/-6; 19 females)
Outcomes:
Outcomes included the Shoulder Pain and Disability Index (SPADI) and measurement of active and passive range of motion (AROM and PROM)in four directions: forward flexion, abduction from standing, external/internal rotation from 45 deg abduction (supine position).
Methods:
RCT: Prospective, Single-Center, Open trial
Time:
Patients were followed up 6 weeks after last injection.
What were the important findings?
  • Both groups had comparable clinical improvements in Shoulder Pain and Disability Index (SPADI), passive range of motion (PROM) and active range of motion (AROM) from baseline (p>0.05).
  • The mean difference in SPADI scores from baseline was 3 points (95% CI: -5 to 11) favouring the DIL group (p>0.05).
  • 13 and 9 patients in the INJ and DIL groups, respectively, reported flushing or disturbances with heat regulation. 20 and 14 patients, respectively, reported pain upon injection.
What should I remember most?

Similar improvements from baseline in Shoulder Pain and Disability Index (SPADI), passive range of motion (PROM) and active range of motion (AROM) were observed in both the hydrodilatation and control groups.

How will this affect the care of my patients?

The results indicated that hydrodilatation did not provide any additional clinical benefits in patients with adhesive capsulitis, but may have an important treatment effect in some selected cases. Therefore, there is a need for future trials investigating the long-term effects of hydrodilatation.

DISCLAIMER

This content found on this page is for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. If you require medical treatment, always seek the advice of your physician or go to your nearest emergency department. The opinions, beliefs, and viewpoints expressed by the individuals on the content found on this page do not reflect the opinions, beliefs, and viewpoints of OrthoEvidence.

0 of 4 monthly FREE articles unlocked
You've reached your limit of 4 free articles views this month

Access to OrthoEvidence for as little as $1.99 per week.

Stay connected with latest evidence. Cancel at any time.
  • Critical appraisals of the latest, high-impact randomized controlled trials and systematic reviews in orthopaedics
  • Access to OrthoEvidence podcast content, including collaborations with the Journal of Bone and Joint Surgery, interviews with internationally recognized surgeons, and roundtable discussions on orthopaedic news and topics
  • Subscription to The Pulse, a twice-weekly evidence-based newsletter designed to help you make better clinical decisions
Upgrade
Welcome Back!
Forgot Password?
Start your FREE trial today!

Your account will be affiliated with
and includes free access to OrthoEvidence


OR
Forgot Password?

OR
Please check your email

If an account exists with the provided email address, a password reset email will be sent to you. If you don't see an email, please check your spam or junk folder.

For further assistance, contact our support team.

Please login to enable this feature

To access this feature, you must be logged into an active OrthoEvidence account. Please log in or create a FREE trial account.

Translate ACE Report

OrthoEvidence utilizes a third-party translation service to make content accessible in multiple languages. Please note that while every effort is made to ensure accuracy, translations may not always be perfect.

How to cite this ACE Report

OrthoEvidence. Dilatation combined with steroid injections equivalent to steroid in adhesive capsulitis. OE Journal. 2013;1(2):149. Available from: https://myorthoevidence.com/AceReport/Show/dilatation-combined-with-steroid-injections-equivalent-to-steroid-in-adhesive-capsulitis

Copy Citation
Please login to enable this feature

To access this feature, you must be logged into an active OrthoEvidence account. Please log in or create a FREE trial account.

Premium Member Feature

To access this feature, you must be logged into a premium OrthoEvidence account.

Share this ACE Report