Abstract
RESUMOObjetivo:validar instrumento para vigilância pós-alta por contato telefônico de cirurgias vídeo-assistidas.Método:estudo multi-métodos com elaboração, validação e aplicação de instrumento. A validação foi realizada por peritos considerando pertinência, clareza e abrangência do conteúdo, sob cálculo do índice de validade de conteúdo, sendo válidas as questões com 80% de concordância. Para aplicação do instrumento, a amostra foi composta por 68 mulheres submetidas à cirurgia vídeo-assistidas sendo realizada análise descritiva.Resultados:houve discordância entre peritos na primeira avaliação e o instrumento foi reformulado obtendo-se concordância na segunda avaliação. A taxa de resposta ao contato telefônico foi de 88,2% (60/68). Queixas de dor abdominal, sangramento e edema incisional foram mais frequentes. Nenhuma apresentou infecção.Conclusão:o instrumento foi validado, aplicado e encontra-se disponível para utilização.
Highlights
Surgical site infection (SSI) is an important public health issue among the infections related to health care based on its high incidence and associated repercussions[1,2]
First stage The content validity index (CVI) or percentage of agreement adopted in this study was 80%
Items with a CVI less than 80% on relevance or clarity or both were reformulated or deleted as suggested by the experts, and the instrument was resubmitted for evaluation
Summary
Surgical site infection (SSI) is an important public health issue among the infections related to health care based on its high incidence and associated repercussions[1,2]. The SSIs are those involving tissue, organ or cavities manipulated during surgery[2], and approximately 60% are preventable[3]. Invasive surgery requiring a short hospital stay and the choice of outpatient surgeries have increased. According to the Centers for Disease Control and Prevention (CDC) [5], the occurrence of SSI should be monitored during hospitalization and after discharge for a period of 30 days or up to one year in the case of implants. New definitions of SSI criteria, adopted by the CDC[6] and the Epidemiological Surveillance Center of São Paulo[7], suggest a post discharge surveillance of 30-90 days for deep incisional SSI or body or space for some procedures, including laparoscopic procedures[7]
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