Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Patients with a non-ST-segment elevation acute coronary syndrome (NSTE-ACS) are currently transported and admitted to the nearest emergency department (ED) for risk stratification, diagnostic workup, and treatment. Recently, several prospective studies have been performed on the diagnostic performance of point-of-care (POC)-troponin and combined risk scores (CRS) for pre-hospital risk assessment and triage of NSTE-ACS patients. Also the first intervention trials on triage decisions based on POC troponin and CRS have been performed. Initial results are indicating that prehospital triage based on these diagnostic tools is feasible and safe, although sample sizes were relatively small and underpowered to detect differences in major adverse cardiac events (MACE). The objective of this individual patient data meta-analysis is to determine the diagnostic performance of POC troponin and combined risk scores for prehospital risk assessment and triage in suspected NSTE-ACS patients.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Usual care | Other | Patients who receive usual care by EMS protocols |
|
| point-of-care troponin | Other | Patients in who risk-stratification was performed by the use of a point-of-care troponin in the EMS setting |
|
| Combined risk scores | Other | Patients in who risk-stratification was performed by the use of a combined risk score in the EMS setting |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Combined risk score | Device | Prehospital risk stratification by the use of a combined clinical risk score including POC-troponin |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with the diagnosis NSTE-ACS | Diagnosis of NSTE-ACS (NSTEMI or unstable AP) during index hospitalization (as assessed by the treating physician) | During index hospitalization, up to 1 day in the ED |
| MACE | All cause death, myocardial infarction, revascularization | Within 30 days |
| Measure | Description | Time Frame |
|---|---|---|
| MACE | All cause death, myocardial infarction, revascularization | 1 week |
| All cause death | Within 30 days and 1 year follow-up | |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Pieter-Jan Vlaar, MD, PhD | Catharina Ziekenhuis Eindhoven | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Catharina hospital Eindhoven | Eindhoven | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35383078 | Background | Demandt JPA, Zelis JM, Koks A, Smits GHJM, van der Harst P, Tonino PAL, Dekker LRC, van Het Veer M, Vlaar PJ. Prehospital risk assessment in patients suspected of non-ST-segment elevation acute coronary syndrome: a systematic review and meta-analysis. BMJ Open. 2022 Apr 5;12(4):e057305. doi: 10.1136/bmjopen-2021-057305. | |
| 34373266 |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Usual care | Other | Prehospital risk stratification by EMS protocols |
|
| point-of-care troponin | Device | Prehospital risk stratification by the use of a POC-troponin |
|
| The number of participants undergoing invasive coronary angiography |
| During or after index hospitalisation, up to 30 days |
| The number of participants undergoing coronary revascularisation | percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) | During or after index hospitalisation, up to 30 days |
| Alternative diagnoses other than NSTE-ACS | If no NSTE-ACS is diagnosed, what is the alternative diagnosis (such as pulmonary embolism, aortic dissection, pneumothorax) | during 30 day follow-up after inclusion |
| Safety endpoints concerning intracoronary angiography and/or PCI | Bleeding complications | during 30 day follow-up after intracoronary angiography and/or PCI |
| Safety endpoints concerning intracoronary angiography and/or PCI | Contrast-induced nephropathy Possible or definite stent thrombosis Ischemic stroke Death | during 30 day follow-up after intracoronary angiography and/or PCI |
| Safety endpoints concerning intracoronary angiography and/or PCI | Possible or definite stent thrombosis | during 30 day follow-up after intracoronary angiography and/or PCI |
| Safety endpoints concerning intracoronary angiography and/or PCI | Ischemic stroke | during 30 day follow-up after intracoronary angiography and/or PCI |
| Safety endpoints concerning intracoronary angiography and/or PCI | Death | during 30 day follow-up after intracoronary angiography and/or PCI |
| Health care utilization | Number of ambulance transfers | Within 30 days after inclusion |
| Health care utilization | Duration of hospitalisation (days) | Up to 30 days after inclusion |
| Health care utilization | Number of double invasive coronary angiography procedures | Within 30 days after inclusion |
| Total health care costs | At 30 days |
| Sagel D, Vlaar PJ, van Roosmalen R, Waardenburg I, Nieuwland W, Lettinga R, van Barneveld R, Jorna E, Kijlstra R, van Well C, Oomen A, Bartels L, Anthonio R, Hagens V, Hofma S, Gu Y, Drenth D, Addink R, van Asselt T, van der Meer P, Lipsic E, Juarez Orozco L, van der Harst P. Prehospital risk stratification in patients with chest pain. Emerg Med J. 2021 Nov;38(11):814-819. doi: 10.1136/emermed-2020-210212. Epub 2021 Aug 9. |
| 36755110 | Background | Camaro C, Aarts GWA, Adang EMM, van Hout R, Brok G, Hoare A, Rodwell L, de Pooter F, de Wit W, Cramer GE, van Kimmenade RRJ, Damman P, Ouwendijk E, Rutten M, Zegers E, van Geuns RM, Gomes MER, van Royen N. Rule-out of non-ST-segment elevation acute coronary syndrome by a single, pre-hospital troponin measurement: a randomized trial. Eur Heart J. 2023 May 14;44(19):1705-1714. doi: 10.1093/eurheartj/ehad056. |
| 34849660 | Background | Tolsma RT, Fokkert MJ, van Dongen DN, Badings EA, van der Sluis A, Slingerland RJ, van 't Riet E, Ottervanger JP, van 't Hof AWJ. Referral decisions based on a pre-hospital HEART score in suspected non-ST-elevation acute coronary syndrome: final results of the FamouS Triage study. Eur Heart J Acute Cardiovasc Care. 2022 Feb 8;11(2):160-169. doi: 10.1093/ehjacc/zuab109. |
| 35863696 | Background | Demandt JPA, Koks A, Haest R, Heijmen E, Thijssen E, Otterspoor LC, van Veghel D, El Farissi M, Eerdekens R, Vervaat F, Pijls NHJ, Veer MVT, Tonino PAL, Dekker LRC, Vlaar PJ. Prehospital triage of patients with suspected non-ST-segment elevation acute coronary syndrome: Rationale and design of the TRIAGE-ACS study. Contemp Clin Trials. 2022 Aug;119:106854. doi: 10.1016/j.cct.2022.106854. Epub 2022 Jul 18. |
| ID | Term |
|---|---|
| D054058 | Acute Coronary Syndrome |
| ID | Term |
|---|---|
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D014652 | Vascular Diseases |
Not provided
Not provided