健康调查简表
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健康调查简表(SF-36)——概况
健康调查简表(Medical Outcomes Study Short Form 36,SF-36)是一种广泛使用的、通用的、患者自评测量工具,旨在评估普通人群的健康相关生活质量(health-related quality of life,HRQOL)。它是作为医学结局研究(Medical Outcomes Study,一项针对慢性病患者的两年研究)的一部分而开发的(Ware & Sherbourne, 1992)。如今,SF-36是用于测量生活质量的最常用通用工具(de Haan, 2002),适用于14岁及以上人群,施测约需10分钟。SF-36可用于但不限于脑卒中患者。该工具为评估工具,证据审核时间截至2008年8月19日之前。
健康调查简表(SF-36)——的目的
SF-36用于评估普通人群及各类疾病人群(包括脑卒中患者)的健康相关生活质量,可自评、计算机施测或由受过训练的访谈者施测。
健康调查简表(SF-36)——的测试项目与分量表
SF-36包含11个问题、共36个条目,分为8个维度:躯体功能(10个条目)、躯体问题导致的角色限制(4个条目)、身体疼痛(2个条目)、总体健康感知(5个条目)、社会功能(2个条目)、总体心理健康(5个条目)、情绪问题导致的角色限制(3个条目)、活力(4个条目)。前4个维度属躯体成分,后4个维度属心理成分。此外还有1个健康变化问题:受访者被要求将当前健康状况与一年前的健康状况进行比较,此问题独立于8个分量表,不参与评分。
回忆期:标准版为过去4周,急性版为过去1周。
健康调查简表(SF-36)——的施测规则
SF-36可自评、计算机施测或由受过训练的访谈者进行面对面或电话施测,也可通过邮寄问卷调查完成。适用于14岁及以上人群(Ware & Sherbourne, 1992)。可通过网络在线评分(付费,QualityMetric网站)。代理施测在脑卒中患者中不推荐,因为一致性差。
健康调查简表(SF-36)——的评分方法
SF-36不适合生成总体总分,推荐使用加权Likert评分系统。各子量表条目相加得到子量表总分,每个分量表的分数经线性转换为0分(负向健康)至100分(正向健康)。可导出躯体成分总分(PCS)和心理成分总分(MCS),但这些总分需谨慎解释:Hobart等(2002)发现这两个量表仅解释SF-36分数方差的60%。
健康调查简表(SF-36)——的测试时间
平均约10分钟完成(Andreson & Meyers, 2000)。
健康调查简表(SF-36)——需要培训吗?
不需要培训即可施测。
健康调查简表(SF-36)——需要什么样的设备?
仅需问卷和铅笔。
健康调查简表(SF-36)——适合哪些患者群体?
可用于:脑卒中患者,但其在脑卒中人群中的适用性存在争议。
不应用于:不能理解书面或口头语言的患者;严重受损的脑卒中幸存者(需要代理完成);失语症患者(应使用SAQOL-39);不应用于记录个体患者变化(仅适用于大群体比较)。
健康调查简表(SF-36)——的心理测量学特性
信度——内部一致性:10项研究中,5项报告优秀内部一致性(除3项研究中的社会功能和1项研究中的总体健康为充分);2项研究报告充分至优秀的内部一致性;3项研究报告差至优秀的内部一致性。详细数据:Brazier et al.(1992)报告大于0.85(优秀),除社会功能0.73;Jenkinson et al.(1993)报告大于0.80(优秀),除社会功能0.76;Jenkinson et al.(1994)报告0.76-0.90;Brazier et al.(1996)报告大于等于0.80,社会功能0.56、总体健康0.66;Essink-Bot et al.(1997)报告0.76-0.91,均值0.84;Weinberger et al.(1996)报告24个中有17个超过0.80;Hagen et al.(2003)在脑卒中患者中报告良好,除1月活力0.68和3月总体健康0.67;Dorman et al.(1998)在2253例脑卒中患者中报告0.81-0.96(优秀);McHorney et al.(1994)报告0.65-0.94,中位数0.85;Anderson et al.(1996)报告0.60-0.90。
重测信度:Brazier et al.(1992)报告0.60-0.81;Brazier et al.(1996)报告0.28-0.70(6个月重测期);Andresen et al.(1999)报告ICC 0.55-0.82;Weinberger et al.(1996)报告r=0.55-0.94;Dorman et al.(1998)在脑卒中患者中报告ICC 0.28-0.80。评分者间信度:无研究检验。
效度——预测效度:总体健康感知最能预测死亡(最低四分位数死亡率是最高四分位数的3倍);基线躯体功能、躯体角色限制和疼痛最能预测住院;疼痛、总体健康和活力最能预测医生就诊;心理健康子量表与抑郁严重程度强烈相关;术前PCS评分是冠状动脉旁路移植术(CABG)术后6个月死亡率的显著预测因子(OR=1.39)。
聚合效度:SF-36躯体健康子量表与日常生活活动指数充分相关;SF-36社会功能与Nottingham健康量表的社会隔离充分相关;SF-36总体健康与EuroQol总体HRQOL评分充分相关;SF-36躯体疼痛与所有EuroQol领域充分相关;角色功能-情绪与EuroQol心理领域充分相关;SF-36躯体健康与老年抑郁量表之间优秀相关;活力子量表与Nottingham健康量表能量子量表优秀相关;躯体疼痛与EuroQol疼痛领域优秀相关。
已知组效度:SF-36评分可区分慢性躯体疾病患者与健康年龄匹配对照、大于75岁与小于75岁个体、不同环境组别(全科对医院门诊)、偏头痛患者与对照、不同就诊频次组、脑卒中患者与年龄性别匹配对照。
地板/天花板效应:8项研究中,6项报告SF-36有显著地板和天花板效应,1项报告仅显著天花板效应,1项报告仅显著地板效应。详细数据:Lai et al.(2003)报告躯体功能地板效应37%-100%,社会功能天花板效应60%;Anderson et al.(1996)报告地板效应无超过7%者,天花板效应为躯体角色限制53%、身体疼痛43%、社会功能67%、情绪角色限制72%;Brazier et al.(1996)报告躯体角色限制和情绪角色限制地板效应大于25%;Hobart et al.(2002)报告躯体角色限制地板效应59.1%、情绪角色限制63.1%、社会功能29.9%、身体疼痛25.6%;O'Mahoney et al.(1998)报告地板效应为躯体角色限制54%、情绪角色限制35%、社会功能17%、躯体功能18%,天花板效应为躯体角色限制16%、情绪角色限制51%、社会功能18%、身体疼痛25%;Weinberger et al.(1996)报告地板效应为躯体角色限制43.8%-53.2%、情绪角色限制25.0%-34.0%,天花板效应为社会功能27.8%-31.5%、躯体角色限制14.6%-14.7%、情绪角色限制36.2%-52.8%;Walters et al.(2001)报告地板效应为躯体角色限制30.9%-60%、情绪角色限制25.6%-50.4%,天花板效应为躯体角色限制11.7%-38.6%、情绪角色限制32.2%-53.2%;Andresen et al.(1999)报告地板效应为躯体功能26.8%、躯体角色限制29.5%,天花板效应为社会功能36.1%、情绪角色限制49.5%、身体疼痛21.6%。
敏感度/变化检测能力:3项研究中,1项报告大变化检测能力,1项报告中等至大变化检测能力(除社会功能和心理健康维度效应量小),1项报告小到大变化检测能力。据知无研究检验SF-36在脑卒中患者中的变化检测能力。
健康调查简表(SF-36)——的版本
SF-36版本1.0(1992年,Ware & Sherbourne):原始版本。
SF-36版本2.0(1996年,SF-36v2):修正了原始版本中发现的缺陷,变更包括措辞修改(如将downhearted and blue改为downhearted and depressed),被认为是SF-36的国际版本(Andresen & Meyers, 2000);回应类别数量和格式标准化;角色功能条目现在有5个回应级别而非2个;早期测试报告为积极(Jenkinson et al., 1999)。
SF-12(Ware, Kosinski, & Keller, 1996):简化版,用于大规模调查,完成时间不超过5分钟,可自评、访谈、电话或计算机施测;SF-12v2与SF-36v2对应。
SF-8(QualityMetric, Inc.):8条目通用评估,每个SF-36维度用1个问题测量,完成时间约1-2分钟,已翻译验证用于30多个国家。
SF-6D(Brazier et al., 1998; 2002):基于偏好的评分系统,使用SF-36的6个子量表,允许从SF-36/SF-36v2计算效用值,将8个维度减至6个(省略总体健康感知,合并躯体和情绪角色限制)。
语言版本:SF-36有多种语言版本。IQOLA项目(1991年启动)有14个国家参与(澳大利亚、比利时、加拿大、丹麦、法国、德国、意大利、日本、荷兰、挪威、西班牙、瑞典、英国、美国),额外翻译用于40多个国家(包括中国、日本、韩国等),超过500篇使用SF-36翻译或英语改编版的出版物。
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