Unknown

Dataset Information

0

Effects of surgery start time on postoperative cortisol, inflammatory cytokines, and postoperative hospital day in hip surgery: Randomized controlled trial.


ABSTRACT: BACKGROUND:The aim of this study was to compare morning surgery (Group A), characterized by high cortisol levels, with afternoon surgery (Group B), characterized by low cortisol levels, with respect to cortisol, inflammatory cytokines (interleukin [IL]-6, IL-8), and postoperative hospital days (POHD) after hip surgery. METHODS:The study was conducted in a single center, prospective, randomized (1:1) parallel group trial. Patients undergoing total hip replacement or hemiarthroplasty were randomly divided into two groups according to the surgery start time: 8 AM (Group A) or 1-2 PM (Group B). Cortisol and cytokine levels were measured at 7:30 AM on the day of surgery, before induction of anesthesia, and at 6, 12, 24, and 48?hours (h) after surgery. Visual analogue scale (VAS) and POHD were used to evaluate the clinical effect of surgery start time. VAS was measured at 6, 12, 24, and 48?h postoperatively, and POHD was measured at discharge. RESULTS:In total, 44 patients completed the trial. The postoperative cortisol level was significantly different between the two groups. (24?h, P?

SUBMITTER: Kwon YS 

PROVIDER: S-EPMC6587638 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Effects of surgery start time on postoperative cortisol, inflammatory cytokines, and postoperative hospital day in hip surgery: Randomized controlled trial.

Kwon Young Suk YS   Jang Ji Su JS   Hwang Sung Mi SM   Tark Hyunjin H   Kim Jong Ho JH   Lee Jae Jun JJ  

Medicine 20190601 24


<h4>Background</h4>The aim of this study was to compare morning surgery (Group A), characterized by high cortisol levels, with afternoon surgery (Group B), characterized by low cortisol levels, with respect to cortisol, inflammatory cytokines (interleukin [IL]-6, IL-8), and postoperative hospital days (POHD) after hip surgery.<h4>Methods</h4>The study was conducted in a single center, prospective, randomized (1:1) parallel group trial. Patients undergoing total hip replacement or hemiarthroplast  ...[more]

Similar Datasets

| S-EPMC7886122 | biostudies-literature
| S-EPMC5820694 | biostudies-literature
| S-EPMC5859856 | biostudies-literature
| S-EPMC7248057 | biostudies-literature
| S-EPMC7502573 | biostudies-literature
| S-EPMC4817082 | biostudies-other
| S-EPMC6991278 | biostudies-literature
| S-EPMC6197795 | biostudies-literature
| S-EPMC6419853 | biostudies-literature
| S-EPMC3403973 | biostudies-literature