Ata Murat Kaynar, Nicole Zharichenko, Ajay D Wasan, Jacques E Chelly
{"title":"基于远程医疗的数字认知行为干预治疗全膝关节置换术围手术期焦虑和抑郁。","authors":"Ata Murat Kaynar, Nicole Zharichenko, Ajay D Wasan, Jacques E Chelly","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Preoperative anxiety and depression have been shown to increase postoperative pain and opioid consumption by up to 50% in patients undergoing primary unilateral Total Knee Arthroplasty (TKA). We hypothesized that the use of a telemedicine-based digital Cognitive Behavioral Intervention program (RxWell<sup>®</sup>) started one month prior to surgery would control anxiety and depression prior to surgery.</p><p><strong>Materials and methods: </strong>This was a randomized, controlled trial that enrolled patients undergoing primary unilateral TKA. At least a month prior to surgery, patients who gave consent to participate were asked to complete PROMIS<sup>®</sup> (Patient-Reported Outcomes Measurement Information System) emotional anxiety short form 8a and PROMIS<sup>®</sup> emotional depression short form-8a questionnaires. Patients with T-scores of ≥ 57 were randomized to either a no intervention (control group) or a RxWell<sup>®</sup> program (treatment group) for a month prior to surgery. The primary outcome of this proof-of-concept study was the ability of the RxWell<sup>®</sup> to normalize patients' PROMIS anxiety T scores.</p><p><strong>Results: </strong>T scores for anxiety and depression among patients randomized to the RxWell<sup>®</sup> group significantly decreased from 64.3 ± 3.0 at the time of randomization to 58.5 ± 2.6 prior to surgery (n=5, p=0.006), whereas no changes in T scores were recorded in the control group (59.4 ± 4.2 at the time of randomization <i>vs</i>. 57.7 ± 6.2; n=6, p=0.559).</p><p><strong>Conclusion: </strong>These preliminary data suggest that the use of a RxWell<sup>®</sup> program represents an effective approach to control anxiety and depression prior to surgery. In contrast, it seems that in the absence of treatment, anxiety level remains similar over a month prior to surgery.</p>","PeriodicalId":90614,"journal":{"name":"Journal of pain & relief","volume":"12 9","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601399/pdf/","citationCount":"0","resultStr":"{\"title\":\"Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.\",\"authors\":\"Ata Murat Kaynar, Nicole Zharichenko, Ajay D Wasan, Jacques E Chelly\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Preoperative anxiety and depression have been shown to increase postoperative pain and opioid consumption by up to 50% in patients undergoing primary unilateral Total Knee Arthroplasty (TKA). We hypothesized that the use of a telemedicine-based digital Cognitive Behavioral Intervention program (RxWell<sup>®</sup>) started one month prior to surgery would control anxiety and depression prior to surgery.</p><p><strong>Materials and methods: </strong>This was a randomized, controlled trial that enrolled patients undergoing primary unilateral TKA. At least a month prior to surgery, patients who gave consent to participate were asked to complete PROMIS<sup>®</sup> (Patient-Reported Outcomes Measurement Information System) emotional anxiety short form 8a and PROMIS<sup>®</sup> emotional depression short form-8a questionnaires. Patients with T-scores of ≥ 57 were randomized to either a no intervention (control group) or a RxWell<sup>®</sup> program (treatment group) for a month prior to surgery. The primary outcome of this proof-of-concept study was the ability of the RxWell<sup>®</sup> to normalize patients' PROMIS anxiety T scores.</p><p><strong>Results: </strong>T scores for anxiety and depression among patients randomized to the RxWell<sup>®</sup> group significantly decreased from 64.3 ± 3.0 at the time of randomization to 58.5 ± 2.6 prior to surgery (n=5, p=0.006), whereas no changes in T scores were recorded in the control group (59.4 ± 4.2 at the time of randomization <i>vs</i>. 57.7 ± 6.2; n=6, p=0.559).</p><p><strong>Conclusion: </strong>These preliminary data suggest that the use of a RxWell<sup>®</sup> program represents an effective approach to control anxiety and depression prior to surgery. In contrast, it seems that in the absence of treatment, anxiety level remains similar over a month prior to surgery.</p>\",\"PeriodicalId\":90614,\"journal\":{\"name\":\"Journal of pain & relief\",\"volume\":\"12 9\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601399/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pain & relief\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/9/27 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pain & relief","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/9/27 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Telemedicine-Based Digital Cognitive Behavioral Intervention for Perioperative Anxiety and Depression for Total Knee Arthroplasty.
Introduction: Preoperative anxiety and depression have been shown to increase postoperative pain and opioid consumption by up to 50% in patients undergoing primary unilateral Total Knee Arthroplasty (TKA). We hypothesized that the use of a telemedicine-based digital Cognitive Behavioral Intervention program (RxWell®) started one month prior to surgery would control anxiety and depression prior to surgery.
Materials and methods: This was a randomized, controlled trial that enrolled patients undergoing primary unilateral TKA. At least a month prior to surgery, patients who gave consent to participate were asked to complete PROMIS® (Patient-Reported Outcomes Measurement Information System) emotional anxiety short form 8a and PROMIS® emotional depression short form-8a questionnaires. Patients with T-scores of ≥ 57 were randomized to either a no intervention (control group) or a RxWell® program (treatment group) for a month prior to surgery. The primary outcome of this proof-of-concept study was the ability of the RxWell® to normalize patients' PROMIS anxiety T scores.
Results: T scores for anxiety and depression among patients randomized to the RxWell® group significantly decreased from 64.3 ± 3.0 at the time of randomization to 58.5 ± 2.6 prior to surgery (n=5, p=0.006), whereas no changes in T scores were recorded in the control group (59.4 ± 4.2 at the time of randomization vs. 57.7 ± 6.2; n=6, p=0.559).
Conclusion: These preliminary data suggest that the use of a RxWell® program represents an effective approach to control anxiety and depression prior to surgery. In contrast, it seems that in the absence of treatment, anxiety level remains similar over a month prior to surgery.