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August 7, 2019European Heart Journal - Quality of Care and Clinical Outcomes8 citations

Acute coronary syndrome registry enrolment status: differences in patient characteristics and outcomes and implications for registry data use (ANZACS-QI 36)

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NENikki EarleAKAndrew KerrMLMalcolm E. Legget

Key Result

First-time ACS patients not captured in the ANZACS-QI registry were more than twice as likely to experience death or non-fatal cardiovascular readmission within 12 months as captured patients.

Study Design

Type

Observational (n=16,569)

Multicenter

Yes

Structured PICO

Are there differences in clinical characteristics and outcomes between first-time ACS patients captured in a clinical registry versus those not captured?

P
Population
16,569 patients admitted with first-time acute coronary syndrome in New Zealand, followed for 12 months to compare outcomes based on registry capture status.
E
Exposure
Captured in the All New Zealand Acute Coronary Syndrome Quality Improvement (ANZACS-QI) registry (n=9,918).
C
Comparator
Not captured in the ANZACS-QI registry.
O
Outcome
Time to 12-month clinical outcomes (death, non-fatal cardiovascular readmission, or composite of death or readmission).hard clinical

First-time ACS patients captured in a national registry have significantly different clinical characteristics and better outcomes than those not captured, highlighting potential selection bias in registry-derived data.

Limitations

  • Cardiovascular registry-derived data are dependent on registry design and may not be representative of the wider patient population

Abstract

AIMS: Clinical registry-derived data are widely used to represent patient populations. In New Zealand (NZ), a national registry-the All New Zealand Acute Coronary Syndrome Quality Improvement (ANZACS-QI) registry-aims to include all patients undergoing coronary angiography; other acute coronary syndrome (ACS) patients are also registered but without complete capture. This study compares national hospitalization data of all first-time ACS admissions in NZ with patients in the ANZACS-QI registry, to investigate the use of clinical registry-derived data in research and in assessing clinical care. METHODS AND RESULTS: Patients admitted with first-time ACS in the NZ National Hospitalisation Dataset between 1 January 2015 and 31 December 2016 were included. Clinical characteristics and time to 12-month clinical outcomes were compared between patients captured and not-captured in the registry. A total of 16 569 patients were admitted with first-time ACS, median age 69 years, 61% male; 60% (n = 9918) were enrolled in ANZACS-QI. Registry-captured patients were younger, more often male, and with a lower comorbidity burden than non-captured patients. Overall, 16% patients died within 12 months, 15% experienced a non-fatal cardiovascular (CV) readmission, and 28% either died or were readmitted. Patients not captured in the registry were more than twice as likely to have experienced death or a non-fatal CV readmission within 12 months as captured patients. CONCLUSIONS: First-time ACS patients captured in the ANZACS-QI registry had very different clinical characteristics and outcomes than those not captured. Cardiovascular registry-derived data are dependent on registry design and may not be representative of the wider patient population; this must be considered when using registry-derived data.

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Cite This Study

Earle et al. (2019) conducted an observational in First-time Acute Coronary Syndrome (n=16,569). ANZACS-QI registry capture vs. Not captured in the registry was evaluated on Death or non-fatal cardiovascular readmission. First-time ACS patients not captured in the ANZACS-QI registry were more than twice as likely to experience death or non-fatal cardiovascular readmission within 12 months as captured patients.

synapsesocial.com/papers/6a22328c1451ae9ed3e246fehttps://doi.org/10.1093/ehjqcco/qcz046
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