2008
DOI: 10.1097/sla.0b013e3181823485
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Successful Implementation of the Department of Veterans Affairs’ National Surgical Quality Improvement Program in the Private Sector: The Patient Safety in Surgery Study

Abstract: The VA NSQIP methods and risk models in general and vascular surgery were fully applicable to PS hospitals. Thirty-day postoperative morbidity in PS hospitals was reduced with the implementation of the NSQIP.

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Cited by 530 publications
(278 citation statements)
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“…The published incidence of adverse events among patients with gynaecological cancer varies from 26% to 54% (13,14) and some studies suggest that a significant portion of AEs are preventable (15)(16)(17).…”
Section: Discussionmentioning
confidence: 99%
“…The published incidence of adverse events among patients with gynaecological cancer varies from 26% to 54% (13,14) and some studies suggest that a significant portion of AEs are preventable (15)(16)(17).…”
Section: Discussionmentioning
confidence: 99%
“…Patient variables from more than 250 participating institutions nationwide are included in the ACS NSQIP 1 , and this database has been used to analyze trends and associations in orthopaedic surgery [15,17,28]. The method of data abstraction from the ACS NSQIP 1 participant files has been described [4,18]. Patients were identified through Current Procedural Terminology (CPT) codes and included patients undergoing TKA (CPT 27447), THA (CPT 27130), single-level posterior or posterolateral lumbar fusion (CPT 22612 with no CPT modifiers), multilevel posterior or posterolateral lumbar fusion (CPT 22612 with a CPT modifier of 22614), single-level anterior cervical discectomy and fusion (CPT 22551 with no CPT modifiers), multilevel anterior cervical discectomy and fusions (CPT 22612 with a CPT modifier of 22552), and total shoulder arthroplasty (CPT 23472).…”
Section: Methodsmentioning
confidence: 99%
“…These patients are prospectively identified and randomly sampled from eligible hospitals in a manner designed by the ACS-NSQIP 1 to minimize selection bias. Data collection occurs for each patient's entire 30-day postoperative period, regardless of the date of discharge after surgery [2,15].…”
Section: Study Design and Settingmentioning
confidence: 99%