Born P H, Thran S L
University of Connecticut, Department of Finance, Storrs 06269-2041, USA.
J Fam Pract. 1998 Apr;46(4):319-27.
The study objectives were to examine the influence of the Clinical Laboratory Improvement Amendments of 1988 (CLIA '88) on laboratory testing activities in physician offices, and to identify relationships between the characteristics of practices and their responses to the regulation.
The data come from a 1995 survey of physician office laboratories conducted by Mathematica Policy Research, and are supplemented by data from a 1991 laboratory survey. Primary care physician practices performing level I and level II tests in 1991 were resurveyed in 1995. Respondents were asked a series of questions pertaining to the types of laboratory tests performed in their offices, and whether CLIA '88 had any influence on the decision to change testing practices. We present descriptive statistics to examine differences across practices in response to CLIA '88. Significant determinants of the decision to drop or modify onsite testing activities are identified using multivariate analysis.
More than 64% of physicians surveyed cited CLIA '88 as a factor in their decision to reduce or eliminate in-office testing. The most striking effect of CLIA '88 appears to be on pediatric practices and practices in rural areas, of which more than 70% have reduced or eliminated onsite testing. Where the potential burden of compliance is smaller, as in large practices, CLIA '88 has had less impact.
CLIA '88 has had significant influence on access to laboratory testing services. According to the data from the 1995 survey, almost two thirds of physicians have eliminated some or all in-office tests. Of those physicians previously conducting in-office tests, 70% have chosen to send patients and specimens to outside facilities, resulting in greater inconvenience for patients and delays in diagnosis and treatment. These delays, and the potential for patient noncompliance stemming from the inconvenience of obtaining tests, have serious implications for the quality of medical care.
本研究的目的是考察1988年《临床实验室改进修正案》(CLIA '88)对医师办公室实验室检测活动的影响,并确定医疗机构特征与其对该法规的应对措施之间的关系。
数据来自1995年由Mathematica政策研究公司对医师办公室实验室进行的一项调查,并辅以1991年实验室调查的数据。对1991年进行一级和二级检测的初级保健医师诊所于1995年进行了重新调查。受访者被问及一系列有关其办公室所进行的实验室检测类型的问题,以及CLIA '88是否对改变检测做法的决定有任何影响。我们给出描述性统计数据以考察各医疗机构对CLIA '88的应对差异。使用多变量分析确定放弃或修改现场检测活动决定的显著决定因素。
超过64%的受访医师将CLIA '88列为其减少或取消办公室内检测决定的一个因素。CLIA '88最显著的影响似乎体现在儿科诊所和农村地区的诊所,其中超过70%已经减少或取消了现场检测。在合规潜在负担较小的地方,如大型诊所,CLIA '88的影响较小。
CLIA '88对实验室检测服务的可及性产生了重大影响。根据1995年调查的数据,近三分之二的医师已经取消了部分或全部办公室内检测。在那些之前进行办公室内检测的医师中,70%选择将患者和样本送到外部机构,给患者带来了更大不便,并导致诊断和治疗延迟。这些延迟以及因检测不便导致患者不依从的可能性,对医疗质量有严重影响。