Patient Safety in Surgery
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ResearchProspective monitoring improves outcomes of primary total hip replacement: a cohort studyPhilipp N Streubel1,2 , Marcela Pachón1 , Carlos A Kerguelén3 , José Navas1,2 , Julio Portocarrero3 , Rodrigo F Pesantez1 , Gamal Zayed1 , Germán Carrillo1 and Adolfo M Llinás1,2  1
Departamento de Ortopedia y Traumatología, Fundación Santa Fe de Bogotá/Universidad de los Andes, Calle 119 No 9-33, Bogotá, Colombia 2
División de Investigación, Banco de Huesos y Tejidos, Fundación Cosme y Damián, Calle 119A No 7-91, Bogotá, Colombia 3
Centro de Gestión Hospitalaria, Carrera 11A No 94-76, Of. 201, Bogotá, Colombia author email corresponding author email
Patient Safety in Surgery 2009,
3:7doi:10.1186/1754-9493-3-7 Abstract
Background
Over the past decade several studies have questioned current standards of patient safety in health care delivery. In response, our institution started a clinical pathway for total hip replacement in 1996. Prospective monitoring with regular feedback sessions to the individuals involved in patient care did however not start until 2003. The present study evaluates the effect of prospective monitoring on outcomes of total hip replacement.
Methods
Clinical records of patients undergoing primary elective total hip replacement between 1997 and 2004 were reviewed. Data on adverse events as well as adherence to protocols for venous thromboembolism prophylaxis were extracted retrospectively for the period 1997 to 2001 and prospectively from 2003 to 2004. Results were compared and analyzed in order to establish possible improvement in outcomes. Data was analyzed with Chi-square or Fisher's Exact test for categorical variables and Student's t-test for continuous variables. Alpha was set as less than 5% and analysis was performed with Stata 9.0 for Macintosh.
Results
Two-hundred and eighty-three patients were included from 1997 to 2001, and 62 from 2003 to 2004. Mean age, male to female ratio and initial diagnosis were similar in both groups. At least one adverse event occurred in 45% of patients in 1997–2001 and in 21% in 2003–2004 (p < 0.001). In-hospital hip dislocations occurred in 6% and 0% (p = 0.05), oliguria in 19% and 5% (p = 0.007), SSI and VTE in 3% and 0% (p = 0.37), adverse drug reactions in 11% and 13% (p = 0.66) and non-adherence to VTE prophylaxis protocols in 15% and 2% of cases respectively (p = 0.002).
Conclusion
Overall rate of adverse events as well as in-hospital hip dislocations, oliguria and non-adherence to VTE prophylaxis protocols were significantly reduced during the second period. We conclude that clinical pathways alone are insufficient to improve patient safety and require prospective monitoring and continuous feedback to health care providers in order to achieve the desired effect. |