RESUMO
BACKGROUND: The objective of this study was to determine the effects of using the Surgical Risk Preoperative Assessment System (SURPAS) on patient satisfaction and surgeon efficiency in the surgical informed consent process, as compared to surgeons' "usual" consent process. STUDY DESIGN: Patient perception of the consent process was assessed via survey in 2 cohorts: 10 surgeons in different specialties used their "usual" consent process for 10 patients; these surgeons were then taught to use SURPAS, and they used it during the informed consent process of 10 additional patients. The data were compared using Fisher's exact test and the Cochran-Mantel-Haenszel test. RESULTS: One hundred patients underwent the "usual" consent process (USUAL), and 93 underwent SURPAS-guided consent (SURPAS). Eighty-two percent of SURPAS were "very satisfied" and 18% were "satisfied" with risk discussion vs 16% and 72% of USUAL, respectively. Of those who used SURPAS, 75.3% reported the risk discussion made them "more comfortable" with surgery vs 19% of USUAL, and 90.3% of SURPAS users reported "somewhat" or "greatly decreased" anxiety vs 20% of USUAL. All p values were <0.0001. Among SURPAS patients, 97.9% reported "enough time spent discussing risks" vs 72.0% of USUAL patients. CONCLUSIONS: The SURPAS tool improved the informed consent process for patients compared with the "usual" consent process, in terms of patient satisfaction, ie making patients feel more comfortable and less anxious about their impending operations. Providers should consider integrating the SURPAS tool into their preoperative consent process.
Assuntos
Consentimento Livre e Esclarecido , Satisfação do Paciente , Complicações Pós-Operatórias/epidemiologia , Cuidados Pré-Operatórios , Adulto , Idoso , Estudos de Coortes , Tomada de Decisões , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Medição de Risco , Inquéritos e QuestionáriosRESUMO
BACKGROUND: With inpatient length of stay decreasing, discharge destination after surgery can serve as an important metric for quality of care. Additionally, patients desire information on possible discharge destination. Adequate planning requires a multidisciplinary approach, can reduce healthcare costs and ensure patient needs are met. The Surgical Risk Preoperative Assessment System (SURPAS) is a parsimonious risk assessment tool using 8 predictor variables developed from the American College of Surgeons (ACS) National Surgical Quality Improvement Program (NSQIP) dataset. SURPAS is applicable to more than 3,000 operations in adults in 9 surgical specialties, predicts important adverse outcomes, and is incorporated into our electronic health record. We sought to determine whether SURPAS can accurately predict discharge destination. STUDY DESIGN: A "full model" for risk of postoperative "discharge not to home" was developed from 28 nonlaboratory preoperative variables from ACS NSQIP 2012-2017 dataset using logistic regression. This was compared with the 8-variable SURPAS model using the C index as a measure of discrimination, the Hosmer-Lemeshow observed-to-expected plots testing calibration, and the Brier score, a combined metric of discrimination and calibration. RESULTS: Of 5,303,519 patients, 447,153 (8.67%) experienced a discharge not to home. The SURPAS model's C index, 0.914, was 99.24% of that of the full model's (0.921); the Hosmer-Lemeshow plots indicated good calibration and the Brier score was 0.0537 and 0.0514 for the SUPAS and full model, respectively. CONCLUSIONS: The 8-variable SURPAS model preoperatively predicts risk of postoperative discharge to a destination other than home as accurately as the 28 nonlaboratory variable ACS NSQIP full model. Therefore, discharge destination can be integrated into the existing SURPAS tool, providing accurate outcomes to guide decision-making and help prepare patients for their postoperative recovery.