{"title":"Controversies surrounding reflex sympathetic dystrophy: a review article.","authors":"R P Pawl","doi":"10.1007/s11916-000-0102-7","DOIUrl":null,"url":null,"abstract":"<p><p>The topic of reflex sympathetic dystrophy (RSD) has generated an increasingly significant volume of medical literature and controversy over the last decade. A search of PubMed, the online site of the National Library of Medicine, for papers on RSD reveals nearly 2200 articles on the topic (using algodystrophy as the search word, wherein RSD references are also included, and more older and European articles are also listed). From 1991 through 1998 inclusive there is an average of nearly 100 articles per year on the topic, which represents more than a third of all the articles referenced since 1965. In the decade of the 1980s, there is an average of 64 articles per year, 74 per year in the last half of the decade and 54 per year in the first half. Prior to the decade of the 1980s, one finds an average of 40 articles per year back to the mid-1960s. The controversy surrounding the disorder centers around the nature of the problem and whether it is a primary organic disorder or a primary psychogenic disorder associated with the accomplishment of some secondary gain. If it is the former, then clearly research should continue to determine the nature and etiology of the malfunctioning organ(s). If, on the other hand, RSD is a psychogenic disorder, then the medical community does well to focus mainly on the peripheral manifestations of the problem. In that instance, therapy should be primarily psychological and cognitive with regard to the secondary gain, and persistent organic treatments are unlikely to improve the condition in general and worsen individual cases.</p>","PeriodicalId":80271,"journal":{"name":"Current review of pain","volume":"4 4","pages":"259-67"},"PeriodicalIF":0.0000,"publicationDate":"2000-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s11916-000-0102-7","citationCount":"34","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current review of pain","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s11916-000-0102-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 34
Abstract
The topic of reflex sympathetic dystrophy (RSD) has generated an increasingly significant volume of medical literature and controversy over the last decade. A search of PubMed, the online site of the National Library of Medicine, for papers on RSD reveals nearly 2200 articles on the topic (using algodystrophy as the search word, wherein RSD references are also included, and more older and European articles are also listed). From 1991 through 1998 inclusive there is an average of nearly 100 articles per year on the topic, which represents more than a third of all the articles referenced since 1965. In the decade of the 1980s, there is an average of 64 articles per year, 74 per year in the last half of the decade and 54 per year in the first half. Prior to the decade of the 1980s, one finds an average of 40 articles per year back to the mid-1960s. The controversy surrounding the disorder centers around the nature of the problem and whether it is a primary organic disorder or a primary psychogenic disorder associated with the accomplishment of some secondary gain. If it is the former, then clearly research should continue to determine the nature and etiology of the malfunctioning organ(s). If, on the other hand, RSD is a psychogenic disorder, then the medical community does well to focus mainly on the peripheral manifestations of the problem. In that instance, therapy should be primarily psychological and cognitive with regard to the secondary gain, and persistent organic treatments are unlikely to improve the condition in general and worsen individual cases.
反射性交感神经营养不良(RSD)的话题在过去十年中产生了越来越多的医学文献和争议。在国家医学图书馆(National Library of Medicine)的在线网站PubMed上搜索有关RSD的论文,发现了近2200篇有关该主题的文章(使用algodystrophy作为搜索词,其中也包括RSD参考文献,以及更多更早的和欧洲的文章)。从1991年到1998年,每年平均有近100篇关于这个主题的文章,占1965年以来所有被引用文章的三分之一以上。在1980年代的十年中,平均每年有64篇文章,该十年的后半年每年74篇,前半年每年54篇。在20世纪80年代之前,人们发现平均每年有40篇文章追溯到20世纪60年代中期。围绕这种障碍的争论集中在问题的本质上,以及它是一种原发性器质性障碍还是一种与某些次要收益相关的原发性心因性障碍。如果是前者,那么显然研究应该继续确定器官功能障碍的性质和病因。另一方面,如果RSD是一种心因性障碍,那么医学界应该把重点放在问题的外围表现上。在这种情况下,治疗应该主要是心理和认知方面的继发性增益,持续的有机治疗不太可能改善一般情况,并使个别病例恶化。