Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Karagoumis et al, 1990 | N = 71 Patients with cardiac sounding chest pain, transported by EMS | PRCT | On scene times | ECG – 16.4+/- 9.7 min No ECG – 16.1 +/- 7 mins | Small numbers No power study |
Transport time | ECG 18.2 mins No ECG 17.6 mins | ||||
Time to thrombolysis | ECG 48+/- 12 mins No ECG 68+/- 29 mins | ||||
Kareiakaes et al, 1992, USA | N = 132 Patients with cardiac chest pain in Emergency Department Or calling for 911 transport | Prospective Cohort | In hospital time delay from arrival to treatment (25th – 75th centile) | Walk In = 64 minutes (46-87 mins) Other ambulance = 55 mins (45-68) EMS – no ECG = 50 mins (38-81 mins) EMS with ECG = 30 mins (27-35 mins) | V small numbers actually randomized Randomization method not clear Lack of power in study therefore unable to demonstrate statistically significant differences |
Aufderheide et al, 1994, USA | N = 680 All patients with chest pain (cardiac sounding) | Prospective Cohort | On scene times by Paramedics | Study 29 +/- 7 mins Control 25 +/- 6 mins | One third of eligible patients excluded High rate of failed transmissions (22%) Retrospective control group from 6 months before |
Time savings – from potential pre-hospital treatment | 101 +/- 81 mins | ||||
Melville et al, 1998, UK | N = 100 Consecutive patients with chest pain suggestive of AMI over 3 month period | Prospective Cohort | Median door to needle time savings | Study – 22 mins Controls – 28 mins (6 minutes saved) | 100 ECG's ?Convenient numbers Used historic control over 3 years previously Time saved not directly attributable to ECG's since bypassing A&E reduced time (DTN) |
Canto et al, 1997, USA | Voluntary data base of patients with AMI – from participating hospitals2 year period N = 275,046 | Retrospective Cohort | Pain to 1st ECG | ECG – 120 mins No ECG – 108 mins | Non consecutive patient enrolment group Pre-hospital ECG group included variable sources GP office to EMS Not all hospitals included in register Possible bias from rural/urban differences Small percent (5%) with pre-hospital ECG's. Groups significantly different |
Median door to PTCA time | ECG – 92 mins No ECG – 115 mins | ||||
Median door to thrombolysis time | ECG – 30 mins No ECG – 40 mins | ||||
Hospital morbidity & mortality | No significant difference | ||||
Brown and Galloway, 2000, Australia | Patients with suspected acute MI where studies looked at pre-hospital ECG usage | Systematic review | Door to needle times | Consistently improved | Only looked at Medline (single database) Conclusion not consistent with results No report on authors assessing validity of studies |
Pre-hospital delays associated with 12-lead acquisition | Minimal delays 1-3 mins | ||||
Ioannidis JP et al, 2001, Boston | Chest pain patients requiring an ECG | Meta-analysis | Clinical effect of pre-hospital thrombolysis coupled with pre-hospital ECG | Time reduction approx 50 mins Mortality not affected Left ventricular ejection fraction - not affected | Wide variety of methodology and different end points Heterogeneity in study results not fully explored |
Foster DB et al, 1994, USA | N = 155 Consecutive patients who had cardiac sounding chest pain over14 months | Prospective Cohort | Door to needle times | ECG 22 +/- 13.8 mins Controls 51 +/- 50 mins | Historical controls Small numbers |
On scene times | ECG 14 +/- 5.1 mins Controls 11.5 +/- 4.9 mins | ||||
Miller-Craig et al, 1997, UK | Phase I N = 124 Phase II N = 123 Patients suspected of having acute MI | Prospective Controlled Study | Interval durations for call to thrombolysis and door to needle times | Call to needle time control vs test 154 vs 93 mins Door to needle time control vs test 97 vs 37 mins | Controls and test patients done during different phases of study – not done concurrently Not randomized The Phase II patients bypass A&E Dept therefore physically shortening DTN times |