Cardinality matching versus propensity score matching for addressing cluster-level residual confounding in implantable medical device and surgical epidemiology: a parametric and plasmode simulation study.

IF 3.9 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES BMC Medical Research Methodology Pub Date : 2024-11-22 DOI:10.1186/s12874-024-02406-z
Mike Du, Stephen Johnston, Paul M Coplan, Victoria Y Strauss, Sara Khalid, Daniel Prieto-Alhambra
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Abstract

Background: Rapid innovation and new regulations lead to an increased need for post-marketing surveillance of implantable devices. However, complex multi-level confounding related not only to patient-level but also to surgeon or hospital covariates hampers observational studies of risks and benefits. We conducted parametric and plasmode simulations to compare the performance of cardinality matching (CM) vs propensity score matching (PSM) to reduce confounding bias in the presence of cluster-level confounding.

Methods: Two Monte Carlo simulation studies were carried out: 1) Parametric simulations (1,000 iterations) with patients nested in clusters (ratio 10:1, 50:1, 100:1, 200:1, 500:1) and sample size n = 10,000 were conducted with patient and cluster level confounders; 2) Plasmode simulations generated from a cohort of 9981 patients admitted for pancreatectomy between 2015 to 2019 from a US hospital database. CM with 0.1 standardised mean different constraint threshold (SMD) for confounders and PSM were used to balance the confounders for within-cluster and cross-cluster matching. Treatment effects were then estimated using logistic regression as the outcome model on the obtained matched sample.

Results: CM yielded higher sample retention but more bias than PSM for cross-cluster matching in most scenarios. For instance, with ratio of 100:1, sample retention and relative bias were 97.1% and 26.5% for CM, compared to 82.5% and 12.2% for PSM. The results for plasmode simulation were similar.

Conclusions: CM offered better sample retention but higher bias in most scenarios compared to PSM. More research is needed to guide the use of CM particularly in constraint setting for confounders for medical device and surgical epidemiology.

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在处理植入式医疗器械和手术流行病学中的群集级残余混杂问题时,卡片匹配与倾向得分匹配的比较:一项参数和质点模拟研究。
背景:快速的创新和新的法规导致对植入式设备上市后监测的需求增加。然而,复杂的多层次混杂因素不仅与患者水平有关,还与外科医生或医院的协变量有关,这阻碍了对风险和收益的观察研究。我们进行了参数和质谱模拟,比较了心因匹配(CM)与倾向得分匹配(PSM)的性能,以减少存在群组级混杂情况下的混杂偏差:方法:进行了两项蒙特卡罗模拟研究:1)参数模拟(1000 次迭代),患者嵌套在组群中(比例为 10:1、50:1、100:1、200:1、500:1),样本量 n = 10,000 例,患者和组群水平混杂因素;2)质谱模拟,从美国医院数据库中选取 2015 年至 2019 年期间入院接受胰腺切除术的 9981 例患者进行模拟。CM采用0.1的混杂因素标准化均值差异约束阈值(SMD),PSM用于平衡群组内和跨群组匹配的混杂因素。然后使用逻辑回归作为结果模型,对获得的匹配样本进行治疗效果估算:在大多数情况下,与 PSM 相比,CM 的样本保留率更高,但跨群组匹配的偏差更大。例如,在比例为 100:1 时,CM 的样本保留率和相对偏差分别为 97.1%和 26.5%,而 PSM 的样本保留率和相对偏差分别为 82.5%和 12.2%。等离子体模拟的结果与此类似:结论:与 PSM 相比,CM 能更好地保留样本,但在大多数情况下偏差较大。需要更多的研究来指导 CM 的使用,特别是在医疗设备和手术流行病学的混杂因素限制设置中。
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来源期刊
BMC Medical Research Methodology
BMC Medical Research Methodology 医学-卫生保健
CiteScore
6.50
自引率
2.50%
发文量
298
审稿时长
3-8 weeks
期刊介绍: BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.
期刊最新文献
The role of the estimand framework in the analysis of patient-reported outcomes in single-arm trials: a case study in oncology. Cardinality matching versus propensity score matching for addressing cluster-level residual confounding in implantable medical device and surgical epidemiology: a parametric and plasmode simulation study. Establishing a machine learning dementia progression prediction model with multiple integrated data. Correction: Forced randomization: the what, why, and how. Three new methodologies for calculating the effective sample size when performing population adjustment.
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