Scharfe Julia, Pfisterer-Heise Stefanie, Pachanov Alexander, Kugler Charlotte Mareike, Mathes Tim, Zhang Zhentian, Morche Johannes, Pieper Dawid
Institute for Health Services and Health Systems Research, Center for Health Services Research Brandenburg, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany.
Institute for Health Services and Health Systems Research, Center for Health Services Research Brandenburg, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany
BMJ Open. 2025 May 6;15(5):e090152. doi: 10.1136/bmjopen-2024-090152.
The relationship between the volume of medical procedures conducted in hospitals and the resulting health outcomes has been described for various surgical and non-surgical medical interventions. As a policy response to this, several countries have implemented minimum volume standards. However, there is currently a lack of systematically compiled evidence assessing their impact. To close this research gap, we conducted a systematic review on the effects of minimum volume standards in hospitals.
Systematic review using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach.
MEDLINE, PubMed Central and Bookshelf (PubMed), EMBASE (Elsevier), CENTRAL (Cochrane Library), CINHAL (EBSCO), EconLIT (EBSCO), PDQ-Evidence for Informed Health Policymaking, Health Systems Evidence and three trial registries were searched until June 2023. Additionally, manual searches were conducted.
For inclusion in this review, studies must investigate the effects of minimum volume standards. We accepted all categories of outcomes. Following the Cochrane Effective Practice and Organisation of Care (EPOC) criteria, only a strict set of study designs, namely randomised controlled trials, non-randomised controlled trials, controlled before-after studies and interrupted time series studies, were included. No restrictions were placed on language, publication date or publication status.
Two reviewers independently screened titles and abstracts for eligibility, reviewed the full texts and performed data extraction of the included articles. Risk of bias was assessed using the 'Risk Of Bias In Non-Randomised Studies-of Interventions' (ROBINS-I) tool. Certainty of evidence was rated using the GRADE approach. For data synthesis and statistical analyses, we adhered to the EPOC guidance.
We included nine studies into our systematic review. Overall, the outcomes reported in the studies are heterogeneous, which did not allow for a meta-analysis, resulting in a narrative analysis of the found evidence. While travel distance increased and length of stay decreased, other reported outcomes such as complications or reoperations were not affected by the introduction of minimum volume standards. Overall, the risk of bias was considered serious for results on outcomes of seven out of the nine included studies and moderate for the remaining two. The certainty of evidence was rated low for complications, reoperations, length of stay and travel distance and very low for mortality (in-hospital; 30 days).
This systematic review does not provide conclusive evidence on the effects of minimum volume standards in hospitals regarding any outcomes. The certainty of evidence for mortality (in-hospital; 30 days) is very low and low for complications, reoperations and travel distance. The results are based on a relatively small number of studies for most outcomes. There is a need for studies researching the effects of minimum volume standards based on a robust study design.
CRD42022318883.
对于各种外科和非外科医疗干预措施,已阐述了医院所实施医疗程序的量与由此产生的健康结果之间的关系。作为对此的一项政策回应,若干国家已实施了最低量标准。然而,目前缺乏系统汇编的证据来评估其影响。为填补这一研究空白,我们针对医院最低量标准的影响进行了一项系统评价。
采用推荐分级、评估、制定与评价(GRADE)方法进行系统评价。
检索了MEDLINE、PubMed Central和Bookshelf(PubMed)、EMBASE(爱思唯尔)、CENTRAL(考克兰图书馆)、CINHAL(EBSCO)、EconLIT(EBSCO)、用于 informed Health Policymaking的PDQ-Evidence、Health Systems Evidence以及三个试验注册库,检索截至2023年6月。此外,还进行了手工检索。
为纳入本评价,研究必须调查最低量标准的影响。我们接受所有类别的结果。按照考克兰有效实践与护理组织(EPOC)标准,仅纳入一组严格的研究设计,即随机对照试验、非随机对照试验、前后对照研究和中断时间序列研究。对语言、出版日期或出版状态未作限制。
两名评价员独立筛选标题和摘要以确定是否符合纳入标准,审阅全文并对纳入文章进行数据提取。使用“非随机干预研究中的偏倚风险”(ROBINS-I)工具评估偏倚风险。使用GRADE方法对证据的确定性进行评级。对于数据合成和统计分析,我们遵循EPOC指南。
我们将9项研究纳入系统评价。总体而言,各研究报告的结果具有异质性,无法进行Meta分析,因此对所获证据进行叙述性分析。虽然旅行距离增加且住院时间缩短,但其他报告的结果,如并发症或再次手术,并未受到最低量标准引入的影响。总体而言,纳入的9项研究中有7项研究结果的偏倚风险被认为严重,其余2项为中度。并发症、再次手术、住院时间和旅行距离方面证据的确定性被评为低,死亡率(住院期间;30天)方面证据的确定性被评为极低。
本系统评价未提供关于医院最低量标准对任何结果影响的确凿证据。死亡率(住院期间;30天)证据的确定性极低,并发症、再次手术和旅行距离方面证据的确定性为低。大多数结果的结果基于相对较少的研究。需要基于稳健的研究设计开展研究以探究最低量标准的影响。
PROSPERO注册号:CRD42022318883。