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Serious adverse event rates and reoperation after arthroscopic shoulder surgery: population based cohort study

Abstract:

Objective To provide clinicians and patients with accurate risk estimates of serious adverse events after common elective shoulder arthroscopic procedures, including reoperation within one year.

Design Population based cohort study.

Setting Hospital Episode Statistics for NHS England, including civil registration mortality data from the Office for National Statistics.

Participants 288 250 arthroscopic shoulder procedures performed in 261 248 patients aged ≥16 years between 1 April 2009 and 31 March 2017. Elective procedures were grouped into subacromial decompression, rotator cuff repair, acromioclavicular joint excision, glenohumeral stabilisation, and frozen shoulder release.

Main outcome measures The primary outcomes were rates of serious adverse events (mortality, pulmonary embolism, pneumonia, myocardial infarction, acute kidney injury, stroke, and urinary tract infection) requiring inpatient care within 90 days post-surgery. Secondary outcomes were specific adverse event rates at 90 days, and reoperations (including for deep infection) within one year.

Results The overall rate of complications within 90 days after arthroscopic shoulder surgery (including reoperation) was low at 1.2% (95% confidence interval 1.2% to 1.3%), with one in 81 patients at risk, and varied according to type of procedure, from 0.6% (0.5% to 0.8%) for glenohumeral stabilisation to 1.7% (1.5% to 1.8%) for frozen shoulder release. After adjustment for age, comorbidities, and sex, no effect of procedure type was observed. Pneumonia was the most common adverse event (0.3%, 0.3% to 0.4%), with one in 303 patients at risk. Pulmonary embolic events were rare, at 0.1% (0.1% to 0.1%), with one in 1428 patients at risk. At one year, the overall rate for reoperation was 3.8% (3.8% to 3.9%), with one in 26 patients at risk, ranging from 2.7% (2.5% to 3.0%) for glenohumeral stabilisation to 5.7% (5.4% to 6.1%) for frozen shoulder release. The overall rate of further surgery for deep infection was low, at 0.1% (0.1% to 0.1%), with one in 1111 patients at risk, but was higher after rotator cuff repair (0.2%, 0.2% to 0.2%), with one in 526 patients at risk. Over the study period the number of arthroscopic shoulder procedures increased, except for subacromial decompression, which decreased.

Conclusions The findings of this study suggest that risks of serious adverse events associated with common shoulder arthroscopy procedures are low. Nevertheless, serious complications do occur, and include the risk of reoperation in one in 26 patients within one year.

Study registration Clinical.Trials.gov NCT03573765.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1136/bmj-2021-069901

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Botnar Research Centre
Research group:
NIHR Oxford Biomedical Research Centre
Oxford college:
Pembroke College
Role:
Author
ORCID:
0000-0003-1818-5800
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Research group:
NIHR Oxford Biomedical Research Centre
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Research group:
NIHR Oxford Biomedical Research Centre
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Research group:
NIHR Oxford Biomedical Research Centre
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Research group:
NIHR Oxford Biomedical Research Centre
Role:
Author


Publisher:
BMJ Publishing Group
Journal:
British Medical Journal (Clinical Research Ed.) More from this journal
Volume:
378
Article number:
e069901
Place of publication:
England
Publication date:
2022-07-06
Acceptance date:
2022-05-24
DOI:
EISSN:
0959-8138
ISSN:
1759-2151
Pmid:
35938625


Language:
English
Keywords:
Pubs id:
1267038
Local pid:
pubs:1267038
Deposit date:
2023-01-20
ARK identifier:

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