Subacromial decompression as a primary/isolated intervention to treat subacromial pain
Magdalena Moshi , Virginie Gaget , Ross McLeod, Thomas Vreugdenburg
Record ID 32018001208
English
Authors' objectives:
The objective of this report was to evaluate the clinical and economic effectiveness of subacromial
decompression as a primary intervention to treat subacromial pain compared to conservative
management, no treatment and placebo, and to consider legal, social, ethical and organisational
issues associated with limiting access to the procedure.
Authors' results and conclusions:
Clinical evaluation
An existing Cochrane review by Karjalainen was included and critiqued. The meta-analyses
performed in the Cochrane review were replicated, and analyses that could not be replicated were
produced independently using novel data inputs. The clinical evaluation of efficacy outcomes was
informed by 8 randomised controlled trials (RCTs); the clinical evaluation of safety outcomes was
informed by 2 RCTs, 7 non-randomised trials and 12 single-arm trials. Effects reported in this
executive summary are summarised at 12 months using new analyses replicated from the
Cochrane review for pain, function and health-related quality of life (HRQoL), and reported in the
Cochrane review for return to work, return to leisure activities and further progression of
subacromial pain.
Subacromial decompression versus conservative treatment
Six RCTs compared subacromial decompression to conservative treatment (n=614). At 12 months
there were no statistically significant differences reported for pain (low certainty evidence), function
(very low certainty evidence), health-related quality of life (HRQoL) (low certainty evidence), return
to work (very low certainty evidence), return to leisure activities (very low certainty evidence),
progression of subacromial pain (very low certainty evidence). The main reason the evidence was
downgraded was due to the risk of detection and performance bias, as participants were not blinded
to their treatment allocations.
Subacromial decompression versus placebo (sham surgery)
Three RCTs compared subacromial decompression to placebo (n=406). At 12 months there were
no statistically significant differences reported for pain (high certainty evidence), function (high
certainty evidence), HRQoL (high certainty evidence), return to work (moderate certainty evidence),
return to leisure activities (moderate certainty evidence). Progression of subacromial pain was not
reported. The analyses in this section were at a low risk of bias, with some outcomes scored down
due to imprecision.
Subacromial decompression versus no treatment
One RCT compared subacromial decompression to no treatment (n=210). At 12 months, there was
a statistically significant difference in pain (MD=-1.2, 95% CI -2.04, -0.36, moderate certainty
evidence), and a clinically important difference in function (MD=9.5, 95% CI: 2.66, 16.34, moderate
certainty evidence) favouring decompression, but no difference for HRQoL (moderate certainty
evidence), further progression of subacromial pain (moderate certainty evidence). Other outcomes
were not reported. The outcomes in this section were scored down due to risk of detection bias, as
participants were not blinded to their treatment allocation.
Safety
There were no statistically significant differences in the number of adverse events recorded for
subacromial decompression and non-operative treatments (moderate certainty evidence). Serious
adverse events were not reported in the selected RCTs (moderate certainty evidence).
Costs and cost-effectiveness
As the clinical evaluation found no clinically significant improvement in short-term HRQoL for
subacromial decompression compared to placebo and conservative management, a cost
comparison was conducted. The inpatient cost of subacromial decompression surgery of CHF8,633
was higher than the estimated conservative management cost of CHF1,350 (15 physiotherapy
sessions at CHF90 per session). The outpatient delivery of subacromial decompression had a cost
of CHF3,972, comprising CHF1,161 for TARMED 24.0710 arthroscopy and 24.0750
decompression; anaesthesia CHF750; and medicines, consumables and overheads CHF2,061.
This cost was also higher than the cost of conservative management. Subacromial decompression
has no clinical benefit, but has a higher cost, compared to the designated comparator (conservative
management), so offers no economic advantage.
A decision analytic model was developed to quantify the cost-effectiveness of subacromial
decompression for inpatient-delivered rotator cuff disease compared to no treatment using
incremental quality-adjusted life years (QALY). An incremental cost-effectiveness ratio (ICER) of
CHF98,102 per QALY gained was estimated at 12 months for surgery compared to no treatment
using results of the Can Shoulder Arthroscopy Work (CSAW) trial when no adjustment was made
to uneven baseline utilities. With adjustment to these values, the ICER was estimated to be
CHF107,913 per QALY gained. Probabilistic sensitivity analyses (PSA) determined with 49%
probability that subacromial decompression was more cost-effective compared to no treatment
using a hypothetical willingness-to-pay threshold of CHF100,000 per QALY gained. Univariate sensitivity analyses indicated the ICERs were most impacted by high and low QALY gained
estimates, diagnosis-related group (DRG) cost variations and inclusion of costs for the intervention
from the tariff system for outpatient medical services.
A budget impact analysis using four substitution scenarios (in which subacromial decompression
was substituted with no treatment and physiotherapy at different rates) was used to determine the
financial implications of delisting the procedure for the payer. If subacromial decompression is
delisted and half of all patients substitute to physiotherapy, then a net cost saving of CHF10.0 million
would occur in 2020. This saving decreased to CHF9.6 million if 75% of subacromial decompression
patients substituted to physiotherapy in this year, and CHF9.1 million when all patients substitute
to physiotherapy. The saving from subacromial decompression delisting decreases as more
patients are assumed to substitute to alternate treatments.
Social, legal, ethical, organisational issues
Limiting the use of subacromial decompression as a primary intervention to treat subacromial pain
could impact workflow and utilisation of services, due to a likely increase in demand for
physiotherapy services. Additionally, issues are related to how depression and anxiety could impact
patient recovery, as well as how health communication affects a patient’s approach to undergoing
physiotherapy. The final issue related to the possible limitation of subacromial decompression as a
primary intervention, was ensuring that patients from specific population groups (e.g. the elderly)
could access physiotherapy.
Conclusion
The evidence base provides limited to no evidence of clinically important benefits in support of the
use of subacromial decompression as a primary or isolated intervention to treat subacromial pain
compared to conservative treatment, placebo (sham surgery) or no treatment. Delisting the
procedure would result in net cost savings – with the impact sensitive to the proportion of patients
who would substitute to other treatments (physiotherapy) or resort to no treatment.
Details
Project Status:
Completed
Year Published:
2021
URL for published report:
https://www.bag.admin.ch/dam/bag/en/dokumente/kuv-leistungen/leistungen-und-tarife/hta/berichte/h0031impg-hta-report.pdf.download.pdf/h0031impg-hta-report.pdf
URL for additional information:
https://www.bag.admin.ch/bag/en/home/versicherungen/krankenversicherung/krankenversicherung-leistungen-tarife/hta/hta-programm.html
English language abstract:
An English language summary is available
Publication Type:
Full HTA
Country:
Switzerland
MeSH Terms
- Shoulder Impingement Syndrome
- Shoulder Injuries
- Shoulder Pain
- Rotator Cuff
- Rotator Cuff Injuries
- Microvascular Decompression Surgery
Keywords
- subacromial decompression
- subacromial pain
- acriomoplasty
- bursectomy
- shoulder
- shoulder pain
- surgical procedure
- PROMs
- efficacy
- effectiveness
- safety
- costs
- economics
- cost-effectiveness
- budget impact
- legal
- social
- ethical
- organisational
Contact
Organisation Name:
Swiss Federal Office of Public Health (FOPH)
Contact Address:
Federal Office of Public Health, Schwarzenburgstrasse 157, CH-3003 Berne, Switzerland
Contact Name:
Stephanie Vollenweider
Contact Email:
hta@bag.admin.ch
Copyright:
Swiss Federal Office of Public Health
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.