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Vol. 37. Núm. 8.
Páginas 681-690 (agosto 2018)
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Vol. 37. Núm. 8.
Páginas 681-690 (agosto 2018)
Original Article
Open Access
The Stent for Life initiative: Factors predicting system delay in patients with ST-segment elevation myocardial infarction
Iniciativa Stent for Life: fatores preditivos de atraso do sistema em doentes com enfarte do miocárdio com supradesnivelamento do segmento ST
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Hélder Pereiraa,
Autor para correspondência
hhpereira@gmail.com

Corresponding author.
, Fausto J. Pintob, Rita Caléa, Ernesto Pereiraa, Sofia Melloc, Sílvia Vitorinoa, Pedro Jerónimo de Sousaa,f, Bruno Brochadod, Sílvia Monteiroe, Rui Campante Telesf, on behalf of the centers participating in the Stent for Life Initiative Portugal
a Cardiology Department, Hospital Garcia de Orta, Almada, Portugal
b Cardiology Department, CCUL, CAML, University of Lisbon, Lisbon, Portugal
c SFL Project Manager, Lisbon, Portugal
d Cardiology Department, Centro Hospitalar do Porto, Porto, Portugal
e Cardiology Department, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal
f Cardiology Department, Centro Hospitalar de Lisboa Ocidental, Lisbon, Portugal
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Table 1. Characteristics of the study population at the different time points of the survey.
Table 2. Characterization of system delay and other times that influence system delay over the different time points of the survey.
Table 3. Univariate and multivariate log-linear regression analysis of predictors of system delay.
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Abstract
Introduction and Aims

System delay (time between first medical contact and reperfusion therapy) is an indicator of quality of primary percutaneous coronary intervention (pPCI) in ST-segment elevation myocardial infarction (STEMI) patients. This study aimed to assess changes in system delay between 2011 and 2015, and to identify its predictors.

Methods

The study included 838 patients admitted to 18 Portuguese interventional cardiology centers suspected of having STEMI with less than 12 hours’ duration who were referred for primary percutaneous coronary intervention. Data were collected for a one-month period every year from 2011 to 2015. Univariate and multivariate logistic regression models were used to determine predictors of system delay.

Results

No significant changes in system delay were observed during the study. Only 27% of patients had a system delay of ≤90 min. Multivariate analysis identified four predictors of system delay: age ≥75 years (OR 2.57; 95% CI 1.50-4.59; p=0.001), attending a center without pPCI (OR 4.08; 95% CI 2.75-6.10; p<0.001), not calling the national medical emergency number (112) (OR 0.47; 95% CI 0.32-0.68; p<0.001), and Central region (OR 3.43; 95% CI 1.60-8.31; p=0.003).

Conclusions

The factors age ≥75 years, attending a center without pPCI, not calling 112, and Central region were identified as predicting longer system delay. This knowledge may help in planning interventions to reduce system delay and to improve the clinical outcomes of patients with STEMI.

Keywords:
Predictive factors
System delay
ST-segment elevation myocardial infarction
Stent for Life
Resumo
Introdução e objetivos

O «Atraso do Sistema» (tempo decorrido entre o primeiro contacto médico e a terapêutica de reperfusão) tem sido considerado um indicador de qualidade na angioplastia primária (P-PCI) em doentes com enfarte do miocárdio com supradesnivelamento do segmento ST (STEMI). Este estudo tem como objetivo estudar a evolução das características do atraso do sistema entre 2011 e 2015 e identificar os seus preditores.

Métodos

O estudo incluiu 838 doentes com suspeita de STEMI com menos de 12 horas de evolução e propostos para angioplastia primária, que foram admitidos em 18 centros portugueses de cardiologia de intervenção. Estes dados foram recolhidos durante um mês por ano, entre 2011 e 2015. Modelos de regressão linear univariável e multivariável foram usados para identificar os fatores preditivos do atraso do sistema. Ao longo do estudo, não foram observadas diferenças significativas no atraso do sistema.

Resultados

Apenas 27% dos doentes obtiveram um atraso do sistema <90 minutos. A análise multivariável encontrou quatro preditores de atraso do sistema: idade ≥ 75 anos (OR 2,57; CI95% 1,50-4,59; p=0,001), entrada num centro sem P-PCI (OR 4,08; CI95% 2,75-6,10; p<0,001), ligar 112- EMS (OR 0,47; CI95% 0,32-0,68; p<0,001) e Região «Centro» (OR 3,43; CI95% 1,60-8,31; p=0,003).

Conclusões

Os fatores «idade >75 anos», «entrada num centro sem P-PCI», não «ligar para o 112-SEM» e «Região Centro» foram identificados como fatores preditores para maior atraso no sistema. O conhecimento destes fatores permitirá programar intervenções que visem reduzir o atraso do sistema e melhorar os resultados dos doentes com STEMI.

Palavras-chave:
Fatores preditivos
Atraso do sistema
Enfarte do miocárdio com supradesnivelamento do segmento ST
Stent for Life
Abbreviations
CI

confidence interval

ECG

electrocardiogram

EMS

emergency medical services

FMC

first medical contact

IQR

interquartile range

MI

myocardial infarction

OR

odds ratio

pPCI

primary percutaneous coronary intervention

SFL

Stent for Life

STEMI

ST-segment elevation myocardial infarction

Texto Completo
Introduction

Primary angioplasty is the best treatment for ST-segment elevation myocardial infarction (STEMI) patients.1–4 However, even in the most developed countries, with a national hospital network equipped with catheterization laboratories and highly skilled teams working 24/7, primary percutaneous coronary intervention (pPCI) is rarely achieved within 120 min of symptom onset. Efforts therefore need to be made to enable better access to pPCI. For this purpose, it is essential to audit, monitor and assess coronary networks. Primary angioplasty should be conducted within 12 hours of symptom onset, but the greatest benefits are achieved if pPCI is performed within two hours.1,2,4,5

Total ischemic time, defined as time from symptom onset to reperfusion, is a well-established prognostic factor in STEMI patients.6-9 It is divided into two main periods, time from symptom onset to first medical contact (FMC) (patient delay), and time from FMC to pPCI (system delay).4,10

The guidelines suggest door-to-balloon time (time from arrival at a pPCI center to beginning of pPCI) as a measure to assess the hospital's performance in STEMI treatment.1,4,11 However, other studies have reported that reducing this time does not positively impact mortality11 and that delays at other stages also influence infarct size and mortality in STEMI patients.12,13

Studies have reported that longer system delay is associated with higher mortality and morbidity rates in STEMI patients.7,14–16

Stent for Life (SFL) is an initiative by the European Association of Percutaneous Cardiovascular Interventions and the European Society of Cardiology designed to improve the treatment of STEMI patients and to reduce STEMI-related mortality. SFL aims to increase the number of STEMI patients treated by pPCI in countries that join the initiative and to ensure that centers are able to perform pPCI 24/7.17 Portugal has been part of this initiative since 201118 and currently 18 centers in mainland Portugal perform pPCI procedures 24/7.

Various factors influence system delay. Importantly, failure to contact the emergency medical services (EMS) and off-hours presentation lead to longer system delay.19

In the last decade, pPCI rates in Portugal were among the lowest in Western Europe, though in recent years the procedure has been performed more frequently in Portuguese hospitals, suggesting that the country's participation in the SFL initiative has had a positive impact.20

This paper aims to assess changes in system delay since Portugal joined SFL, to identify factors that influence this time, and to identify areas of intervention designed to improve care of STEMI patients.

MethodsStudy design and data collection

The study population was composed of 838 patients suspected of having STEMI with less than 12 hours’ duration who were referred for pPCI and admitted to one of the 18 interventional cardiology centers in mainland Portugal that have 24/7 pPCI and participate in the National Registry of Interventional Cardiology (RNCI) and the Portuguese Registry of Acute Coronary Syndromes (ProACS). The diagnosis of STEMI was confirmed in 90.5% of cases.

The study was based on a national survey involving these centers under the aegis of the Portuguese Association of Interventional Cardiology (APIC). For a one-month period, every year from 2011 to 2015, all patients with STEMI who underwent coronary angiography at the participating centers were enrolled in the study. The survey was carried out at five time points: from May 9 to June 8, 2011, immediately after Portugal joined SFL (time zero, T0), and at the same point in 2012 (time one, T1), 2013 (time two, T2), 2014 (time three, T3) and 2015 (time four, T4). STEMI was defined according to the universal definition of myocardial infarction.21 FMC was defined as the time of arrival of medical and/or paramedical staff to attend the patient or the time of arrival at a hospital for fibrinolysis or pPCI.

Patients who received fibrinolytic therapy prior to pPCI, presented with in-hospital STEMI, were admitted in the autonomous regions of Madeira and the Azores, had late STEMI presentation (more than 12 hours after symptom onset), or did not present ST elevation on the electrocardiogram, were excluded from the study.

Demographic and clinical data were collected. System delay was considered as a continuous or categorical variable, in accordance with international guidelines. The cut-offs used were 120 min for total ischemic time, 90 min for system delay, 60 min for door-to-balloon time and 10 min for FMC-to-electrocardiogram (ECG) time.

Statistical analysis

The normality of data was assessed by the Shapiro-Wilk test. As system delay values were skewed, they were described using medians and interquartile range (IQR) and tested using the Mann-Whitney U test and the Kruskal-Wallis test for two or more independent samples, respectively. Additionally, considering system delay as a categorical variable (≤90 min), number and percentage were used to summarize this variable and differences between groups were assessed by the chi-square test or Fisher's exact test.

For categorical data, differences between groups were assessed by the chi-square test or Fisher's exact test. For continuous and normally distributed data, differences between two or more groups were assessed by the Student's t test or ANOVA, respectively. For non-normally distributed data, the Mann-Whitney test or the Kruskal-Wallis test were used.

Considering system delay as a categorical outcome, its association with each potential predictive factor was first tested in a univariate logistic regression model. Multivariate logistic regression models were then used to determine variables independently associated with system delay, considering all significant predictive factors identified in the univariate model. Odds ratios (OR) and 95% confidence intervals (CIs) were reported. The analysis was conducted at a 5% level of significance. All statistical analyses were performed using R software, version 3.1.0.22

Results

The sample comprised 838 patients who underwent pPCI between 2011 (T0) and 2015 (T4). Patient characteristics over the years are summarized in Table 1. In the last year (T4), patients included in the analysis were older (p=0.048) and had a higher prevalence of diabetes compared to previous years (p=0.032). Although the percentage of patients who called the national medical emergency number (112) did not change, the number of patients admitted to a pPCI center through the EMS tended to increase. By contrast, there was a downward trend in the proportion of patients transferred from local hospitals without pPCI facilities. Of the 319 patients with suspected STEMI who called 112, only 169 (53%) were in fact transported by the EMS (Table 1).

Table 1.

Characteristics of the study population at the different time points of the survey.

Variable    Total  T0  T1  T2  T3  T4 
Total, n (%)    838  157 (18.7)  151 (18.0)  173 (20.6)  195 (23.3)  162 (19.3)   
Region, n (%)North  297  66 (42.0)  54 (35.8)  59 (34.1)  63 (32.3)  55 (34.0)  0.009 
Central  79  22 (14.0)  11 (7.3)  10 (5.8)  14 (7.2)  22 (13.6)   
Lisbon and Tagus Valley  376  59 (37.6)  71 (47.0)  78 (45.1)  97 (49.7)  71 (43.8)   
Algarve  55  10 (6.4)  12 (7.9)  14 (8.1)  10 (5.1)  9 (5.6)   
Alentejo  31  0 (0.0)  3 (2.0)  12 (6.9)  11 (5.6)  5 (3.1)   
Gender, n (%)Male  649  129 (82.2)  119 (82.1)  128 (74.9)  158 (82.7)  115 (72.8)  0.066 
Female  173  28 (17.8)  26 (17.9)  43 (25.1)  33 (17.3)  43 (27.2)   
Age, yearsn (%)  838  155 (18.8)  146 (17.7)  171 (20.7)  193 (23.4)  160 (19.4)   
Mean (SD)  62.1 (13.3)  62.5 (13.7)  60.8 (13.0)  62.8 (13.2)  60.2 (14.0)  64.3 (12.3)  0.040 
Median (IQR61.0 (53.0-71.0)  63.0 (53.0-72.5)  59.0 (52.2-69.0)  60.0 (54.0-71.0)  60.0 (50.0-69.0)  63.0 (55.0-73.0)  0.048 
Median (min-max)  61.0 (1.0-95.0)  63.0 (28.0-95.0)  59.0 (33.0-94.0)  60.0 (19.0-89.0)  60.0 (1.0-94.0)  63.0 (35.0-90.0)   
CV (%)  21.4  21.9  21.3  21.0  23.3  19.1   
Categorized age, n (%)<75 years  671  125 (80.6)  123 (84.2)  138 (80.7)  162 (83.9)  123 (76.9)  0.424 
≥75 years  154  30 (19.4)  23 (15.8)  33 (19.3)  31 (16.1)  37 (23.1)   
History of PCI, n (%)no  730  136 (88.9)  129 (88.4)  150 (87.2)  173 (89.6)  142 (89.9)  0.940 
yes  92  17 (11.1)  17 (11.6)  22 (12.8)  20 (10.4)  16 (10.1)   
History of CABG, n (%)no  810  150 (99.3)  145 (99.3)  172 (100.0)  190 (97.9)  153 (98.1) 
yes  1 (0.7)  1 (0.7)  0 (0.0)  4 (2.1)  3 (1.9)   
History of MI, n (%)no  726  133 (89.3)  127 (87.0)  150 (87.2)  172 (88.7)  144 (91.7)  0.682 
yes  92  16 (10.7)  19 (13.0)  22 (12.8)  22 (11.3)  13 (8.3)   
History of diabetes, n (%)no  651  127 (86.4)  115 (78.2)  134 (77.9)  161 (83.4)  114 (73.1)  0.032 
yes  164  20 (13.6)  32 (21.8)  38 (22.1)  32 (16.6)  42 (26.9)   
Called 112, n (%)no  507  96 (64.4)  90 (59.6)  110 (64.3)  115 (59.3)  96 (59.6)  0.739 
yes  319  53 (35.6)  61 (40.4)  61 (35.7)  79 (40.7)  65 (40.4)   
Hospital triage, n (%)Not applicable  175  22 (14.5)  45 (31.9)  38 (23.3)  36 (19.0)  34 (21.8) 
Manchester  617  130 (85.5)  96 (68.1)  120 (73.6)  151 (79.9)  120 (76.9)   
Other  0 (0.0)  0 (0.0)  5 (3.1)  2 (1.1)  2 (1.3)   
Triage classification, n (%)Red  48  7 (5.8)  11 (11.7)  8 (6.8)  17 (11.3)  5 (4.3)  0.020 
Orange  425  93 (76.9)  64 (68.1)  92 (78.0)  101 (67.3)  75 (64.1)   
Yellow or other  127  21 (17.4)  19 (20.2)  18 (15.3)  32 (21.3)  37 (31.6)   
FMC during off-hours, n (%)No  383  74 (51.4)  65 (43.0)  79 (45.7)  91 (46.7)  74 (45.7)  0.699 
Yes  442  70 (48.6)  86 (57.0)  94 (54.3)  104 (53.3)  88 (54.3)   
Attending a center without pPCI after FMC (secondary transport), n (%)No  443  72 (45.9)  81 (53.6)  89 (51.4)  109 (55.9)  92 (56.8)  0.288 
Yes  395  85 (54.1)  70 (46.4)  84 (48.6)  86 (44.1)  70 (43.2)   
Means of transport to pPCI facility, n (%)Other means of transport  395  85 (54.1)  70 (46.4)  84 (48.6)  86 (44.1)  70 (43.5)  0.058 
EMS from primary healthcare, home or outdoors  169  15 (9.6)  36 (23.8)  37 (21.4)  44 (22.6)  37 (23.0)   
Direct to the pPCI center (non-EMS)  273  57 (36.3)  45 (29.8)  52 (30.1)  65 (33.3)  54 (33.5)   
Diagnosis after team activation, n (%)STEMI  829  156 (99.4)  151 (100.0)  169 (97.7)  192 (98.5)  161 (99.4) 
No significant coronary lesions  1 (0.6)  0 (0.0)  2 (1.2)  0 (0.0)  0 (0.0)   
Myopericarditis  0 (0.0)  0 (0.0)  0 (0.0)  3 (1.5)  1 (0.6)   
Tako-tsubo syndrome  0 (0.0)  0 (0.0)  2 (1.2)  0 (0.0)  0 (0.0)   

p: for difference between groups using a non-parametric Kruskal-Wallis test.

CABG: coronary artery bypass grafting; CV: coefficient of variation; ECG: electrocardiogram; EMS: emergency medical services; FMC: first medical contact; IQR: interquartile range; MI: myocardial infarction; min-max: minimum-maximum; pPCI: primary percutaneous coronary intervention; SD: standard deviation; STEMI: ST-segment elevation myocardial infarction; T0: time zero, 2011; T1: time one, 2012; T2: time two, 2013; T3: time three, 2014; T4: time four, 2015.

Considering only the patients transferred (n=379), there were differences between the time points in those transferred by EMS from another hospital to the pPCI center (inter-hospital transport: 21% vs. secondary transport: 79%) (p<0.001). The percentage of patients using secondary transport decreased throughout the survey (data not shown).

Table 2 presents the characteristics of system delay (FMC-to-ECG time, door-to-balloon time, system delay and total ischemic time) for the different time points. No differences were found between the four time points. The percentage of patients with FMC-to-ECG time <10 min was less than 50% at all time points. Door-to-balloon time <60 min decreased non-significantly from 56.4% to 48.8%. Two hundred and twenty-two patients (26%) had a system delay of ≤90 min and only 70 patients (8%) had total ischemic time of ≤120 min.

Table 2.

Characterization of system delay and other times that influence system delay over the different time points of the survey.

Variable    Total  T0  T1  T2  T3  T4 
Total  n (%)  838  157 (18.7)  151 (18.0)  173 (20.6)  195 (23.3)  162 (19.3)   
FMC-to-ECG time, minn (%)  838  131 (17.9)  136 (18.6)  151 (20.7)  170 (23.3)  142 (19.5)   
Median (IQR13.0 (5.2-30.0)  16.0 (7.5-39.0)  13.0 (5.0-30.0)  12.0 (7.0-29.5)  12.5 (5.0-29.8)  13.0 (5.0-28.8)  0.421 
FMC-to-ECG time ≤10 min, n (%)No  418  86 (65.6)  80 (58.8)  84 (55.6)  90 (52.9)  78 (54.9)  0.225 
Yes  312  45 (34.4)  56 (41.2)  67 (44.4)  80 (47.1)  64 (45.1)   
Door-to-balloon time, minn (%)  838  156 (18.7)  147 (17.6)  173 (20.8)  195 (23.4)  162 (19.4)   
Median (IQR55.0 (30.0-95.0)  54.0 (30.0-96.8)  50.0 (33.5-96.0)  57.0 (30.0-83.0)  57.0 (28.0-101.0)  64.0 (30.0-100.0)  0.883 
Door-to-balloon time ≤60 min, n (%)No  382  68 (43.6)  64 (43.5)  76 (43.9)  91 (46.7)  83 (51.2)  0.585 
Yes  451  88 (56.4)  83 (56.5)  97 (56.1)  104 (53.3)  79 (48.8)   
System delay, minn (%)  838  157 (18.7)  151 (18.0)  173 (20.6)  195 (23.3)  162 (19.3)   
Median (IQR124.0 (89.0-192.0)  115.0 (79.0-179.0)  125.0 (92.5-186.0)  115.0 (87.0-189.0)  130.0 (91.0-217.0)  127.0 (92.5-203.8)  0.304 
System delay ≤90 min, n (%)no  616  107 (68.2)  114 (75.5)  122 (70.5)  147 (75.4)  126 (77.8)  0.260 
yes  222  50 (31.8)  37 (24.5)  51 (29.5)  48 (24.6)  36 (22.2)   
Total ischemic time, minn (%)  838  157 (19.0)  150 (18.1)  172 (20.8)  191 (23.1)  158 (19.1)   
Median (IQR250.0 (171.0-408.5)  250.0 (180.0-421.0)  247.0 (165.0-352.0)  260.5 (165.0-392.2)  240.0 (165.5-430.5)  263.5 (179.2-441.0)  0.542 
Total ischemic time ≤120 min, n (%)No  758  144 (91.7)  132 (88.0)  157 (91.3)  176 (92.1)  149 (94.3)  0.393 
Yes  70  13 (8.3)  18 (12.0)  15 (8.7)  15 (7.9)  9 (5.7)   

p: for difference between groups using a non-parametric test (Kruskal-Wallis).

Door-to-balloon time: time from arrival at a primary percutaneous coronary intervention center to beginning of procedure; ECG: electrocardiogram; FMC: first medical contact; IQR: interquartile range; System delay: time between first medical contact and reperfusion therapy; T0: time zero, 2011; T1: time one, 2012; T2: time two, 2013; T3: time three, 2014; T4: time four, 2015; Total ischemic time: time from symptom onset to reperfusion.

To identify potential factors predicting system delay, univariate and multivariate logistic regression models were used to analyze a set of variables that could influence the outcome (Table 3). The variables T4, female gender, age ≥75 years, Central and Alentejo regions, not calling 112, not arriving by their own means of transport to a pPCI unit, and attending a center without pPCI or other healthcare unit after FMC (patient transferred) were identified as potential factors predicting longer system delay in univariate logistic regression analysis (Table 3). Admission during off-hours periods (nights or weekends) was not significantly associated with longer system delay. In multivariate logistic regression analysis, only age ≥75 years, Central region, not calling 112 and attending a center without pPCI remained statistically significant predictors of longer system delay. Medians and interquartile range of system delay are presented in Figure 1 for each category of these predictive factors with p-values from multivariate logistic regression.

Table 3.

Univariate and multivariate log-linear regression analysis of predictors of system delay.

Variable    n (%)  Univariate modelsMultivariate model
      OR (95% CI)  ORa (95% CI)  pa 
Time pointT0  157 (18.7) 
T1  151 (18.0)  1.44 (0.88-2.38)  0.153  1.31 (0.69-2.51)  0.410 
T2  173 (20.6)  1.12 (0.70-1.79)  0.641  0.87 (0.46-1.63)  0.668 
T3  195 (23.3)  1.43 (0.90-2.29)  0.133  1.32 (0.71-2.44)  0.380 
T4  162 (19.3)  1.70 (1.03-2.82)  0.040  1.50 (0.79-2.87)  0.215 
GenderMale  649 (79.0) 
Female  173 (21.0)  1.73 (1.15-2.67)  0.011  1.40 (0.88-2.29)  0.162 
Categorized age<75 years  671 (81.3) 
≥75 years  154 (18.7)  2.95 (1.82-5.05)  <0.001  2.57 (1.50-4.59)  0.001 
RegionNorth  297 (35.4) 
Central  79 (9.4)  3.22 (1.62-7.18)  0.002  3.43 (1.60-8.31)  0.003 
Lisbon and Tagus Valley  376 (44.9)  1.07 (0.76-1.50)  0.697  1.38 (0.93-2.05)  0.110 
Algarve  55 (6.6)  0.93 (0.50-1.76)  0.809  0.97 (0.47-2.09)  0.938 
Alentejo  31 (3.7)  3.87 (1.33-16.46)  0.029  3.34 (1.05-15.01)  0.067 
History of PCINo  730 (88.8)     
Yes  92 (11.2)  0.76 (0.48-1.24)  0.262     
History of MINo  726 (88.8)     
Yes  92 (11.2)  0.79 (0.50-1.29)  0.338     
History of diabetesNo  651 (79.9)     
Yes  164 (20.1)  0.98 (0.67-1.45)  0.916     
Called 112no  507 (61.4) 
yes  319 (38.6)  0.59 (0.43-0.81)  0.001  0.47 (0.32-0.68)  <0.001 
Arrival by own means of transport at a pPCI centerNo  221 (62.6)  (a)   
Yes  132 (37.4)  0.56 (0.35-0.89)  0.013     
FMC during off-hoursNo  383 (46.4)     
Yes  442 (53.6)  1.31 (0.96-1.79)  0.088     
Attending a center without pPCI or other healthcare unit after FMC (patient transferred)No  295 (39.6) 
Yes  450 (60.4)  3.35 (2.41-4.69)  <0.001  4.08 (2.75-6.10)  <0.001 
Diagnosis of STEMI after team activationNo  9 (1.1)     
Yes  829 (98.9)  0.35 (0.02-1.90)  0.318     
a

Adjusted for all the other covariates presented in the multivariate model.

CI: confidence interval; FMC: first medical contact; MI: myocardial infarction; OR: odds ratio; PCI: percutaneous coronary intervention; pPCI: primary percutaneous coronary intervention; T0: time zero, 2011; T1: time one, 2012; T2: time two, 2013; T3: time three, 2014; T4: time four, 2015.

Only significant variables were included in the multivariate model (except variables with problems of multicollinearity). The variable history of coronary artery bypass grafting was not included because the small number of cases.

Figure 2A shows that there were no significant changes in the number of patients calling 112 over the different time points of the survey (T0-T4) (p=0.739). When stratified according to whether or not patients called 112 (Figure 2B), differences between the groups were found for FMC-to-ECG time (p<0.001), system delay (p=0.001) and total ischemic time (p<0.001). It can also be seen that 32.9% of patients calling 112 had a system delay ≤90 min, which is significantly more than those who did not (22.5%). Similarly, considering as a variable whether the patient was transferred or was taken direct to the pPCI center by the EMS, differences were found for FMC-to-ECG time, system delay and total ischemic time (Figure 3). It can be seen that 33.1% of patients transported directly to a pPCI center by the EMS had a system delay ≤90 min vs. 13.2% of patients who were transferred (p=0.001), which corresponds to 20% more patients who were within the recommended system delay times.

Discussion

System delay is one of the most important timings for assessing the quality of a system, but also for determining which reperfusion strategy should be used.23 Current guidelines suggest pPCI as the ideal reperfusion strategy in STEMI patients, unless it cannot be offered within the recommended timeframes, in which case fibrinolytic therapy should be considered. There is, however, still considerable debate concerning how much delay is acceptable when making this decision, or when a combination of the two reperfusion methods should be preferred.24,25 There is evidence that pPCI loses its advantage over fibrinolysis for longer delays after symptom onset.26

Our results suggest that there were no significant improvements in system delay between the beginning of SFL in Portugal (T0) and 2015 (T4). Furthermore, the study suggests that the aims stated in the current STEMI treatment guidelines1,2 have not been achieved in Portugal: system delay was over 115 min at all the time points of the study, and only 33.1% of STEMI patients transported directly to a pPCI center by EMS had a system delay of 90 min or less. The situation is very different in central and northern Europe. In daily practice in the Netherlands, almost all STEMI patients can be transported to a pPCI center within 60 min of FMC (which is usually the emergency call),27 while in Sweden the median FMC-pPCI time is 70 min.28

Univariate analysis of our results revealed that six factors influence system delay: age ≥75 years, female gender, Central and Alentejo regions, and attending a center without pPCI were associated with longer system delay, whereas the variables calling 112 and arrival by their own means of transport at a pPCI center were associated with shorter system delay. However, the multivariate model showed that only the variables age ≥75 years, Central region, and attending a center without pPCI were predictors of longer system delay, whereas calling 112 was predictive of shorter system delay.

In view of these results, it is important to look at the way elderly patients are handled when they enter the health system. This segment of the population presents specific characteristics that contribute to greater system delay. Low literacy levels, slowness and frailty affect how these patients are handled and transported in and between hospitals, leading to further delays.

The Central region presents significantly longer system delays than other regions of the country. One of the reasons for this result may be the greater distances in this region between the patient's location at the time of symptom onset and the pPCI center. Geographic adjustments in the STEMI network and improvements in transport (direct to a pPCI center and transfer) may lead to more equitable access to pPCI.

The fact that there were more patients who called 112 with system delay ≤90 min than those who did not may have a simple explanation: in the former group, the number of patients who arrive directly at a pPCI center and who spend no time in inter-hospital transfer is likely to be much higher. The fact that in our study patients who called 112 had significantly shorter system delay may be closely related to the SFL initiative in Portugal, as since the beginning of this initiative, the EMS started to contact pPCI centers directly, to transmit ECGs wirelessly, and to deliver STEMI patients directly to catheterization laboratories. This is confirmed by the fact that, in this study, more patients transported by the EMS had an FMC-to-ECG time of ≤10 min than those not transferred by the EMS. A recent study in the USA demonstrated that prehospital wireless electrocardiogram transmission reduced system delay.29 In Denmark, a study conducted between 1999 and 2009 investigated the impact of a gradual introduction of field triage for pPCI and associated outcomes. Among patients transported by the EMS from the scene of the event, the proportion who were triaged directly to a pPCI center in the field increased from 33% to 72%.30 Current guidelines confirm the importance of field triage, stating that the delay between FMC and diagnosis should be reduced to 10 min or less.1

In our study, STEMI patients who initially attended a center without pPCI had significantly longer system delay than those who arrived directly at a pPCI center. Comparison of the variables patient transferred vs. direct to pPCI center by EMS, as they relate to FMC-to-ECG time ≤10 min, system delay ≤90 min, and total ischemic time ≤120 min, suggests that attending a center without pPCI is a strong predictor of prolonged system delay. Significantly more patients transported directly to a pPCI center by the EMS had a system delay of ≤90 min. In the worst-case scenario (patient transferred), prolonged delay is closely related to time spent in the first hospital (door-in-door-out) and with inter-hospital transfer. Some studies suggest that door-in-door-out time is associated with patient management in the emergency room of the non-pPCI hospital.16,31

Although information campaigns to raise awareness of MI have been conducted, many patients still do not call the EMS and arrive at the hospital by their own means.5 However, in some cases admission to a center without pPCI may be through the EMS. This does not always imply a system failure; one study suggested that these delays are often due to diagnostic uncertainty instead. Of patients with suspected STEMI who called 112, only 53% were in fact transported by an EMS ambulance. In the other cases, the national referral center for emergency patients (CODU) did not activate EMS transportation for two main reasons: there were no EMS vehicles available, or the patients were misdiagnosed. In both cases, the patients were transported by the fire department and not by EMS ambulance, as should have occurred. In a Canadian study, patients requiring pPCI and undergoing inter-hospital transfer had longer symptom-call times, lower ECG ST-elevation scores, and more protocol-negative ECGs at presentation.32

Regarding transferred patients, our results suggest a positive trend, with a significant decrease being observed over the course of the study. Nevertheless, there are some actions that can still be implemented to improve the outcomes of transferred patients, as suggested in a five-year study in the USA, in which a program of rapid triage, transfer, and treatment of STEMI patients implemented in a rural area reduced in-hospital mortality and produced progressive improvements in door-to-balloon time.33

Raising public awareness, including strengthening and improving campaigns to publicize the onset of MI symptoms and to encourage people to call the 112 emergency number, could help reduce system delay.

Our results indicate that system delay did not decrease over the course of the SFL initiative, but this does not mean that the initiative was unsuccessful. Over little more than a decade, the use of pPCI tripled in Portugal.34 The first centers to perform pPCI were located in the largest urban centers, which were provided with more than one angiography room. In these urban centers, secondary transport was practically non-existent and few patients called 112. Thus, system delay was estimated on the basis of door-to-balloon time only. The spread of pPCI to peripheral centers and more frequent 112 calls led to an increase in system delay, mainly due to increased use of secondary transport. At the same time, primary transport by EMS also increased, which also increased system delay. In fact, although the system has become more efficient, the clock now starts ticking as soon as FMC occurs, before arrival at the hospital.

In the intermediate stage of such an initiative, while the system is still adapting and expanding, conventional quality indicators such as patient delay, system delay and door-to-balloon time are not sufficiently sensitive to assess how the initiative is developing. The percentages of patients who call 112, who go directly to secondary hospitals and who are transported by EMS may be more sensitive and earlier indicators that can be used to measure a positive evolution.

Our study has some limitations. Data were only collected on patients treated by pPCI, so they cannot be generalized to all STEMI patients. In addition, the survey only covered one month in each year, which means the possible effects of seasonal factors on the results were not addressed. For this reason, future surveys should collect data continuously.

In conclusion, this study showed that system delay did not change significantly during the study period. However, it revealed that the variables age ≥75 years, attending a center without pPCI, and Central region were significantly associated with prolonged system delay, whereas calling 112 was clearly associated with shorter system delay. Based on these factors, objective measures can be taken to reduce system delay and to improve clinical outcomes in Portuguese STEMI patients. However, efforts to improve outcome should not simply address a single quality measurement but should instead embrace a broader spectrum of procedures in MI care.

Centers participating in the Stent for Life Initiative Portugal under the aegis of the Portuguese Association of Interventional Cardiology (APIC):

Hospital Vila Real (Dr. Henrique Cyrne Carvalho and Paulino Sousa), Hospital Braga (Dr. João Costa), Hospital S. João (Dr. João Carlos Silva), Hospital Santo António (Dr. Henrique Cyrne Carvalho), Centro Hospitalar Vila Nova de Gaia (Dr. Vasco Gama Fernandes), Hospital de Viseu (Dr. João Pipa), Centro Hospitalar de Coimbra (Dr. Marco Costa and Dr. Vitor Matos), Hospital de Leiria (Dr. João Morais), Hospital Fernando da Fonseca (Dr. Pedro Farto e Abreu), Hospital de Santa Maria (Dr. Pedro Canas da Silva), Hospital Santa Cruz (Dr. Manuel Almeida), Hospital de Santa Marta (Dr. Rui Ferreira), Hospital Curry Cabral (Dr. Luis Morão), Hospital Pulido Valente (Dr. Pedro Cardoso), Hospital Garcia de Orta (Dr. Hélder Pereira), Hospital Setúbal (Dr. Ricardo Santos); Hospital de Évora (Dr. Lino Patrício and Dr. Renato Fernandes), Hospital de Faro (Dr. Victor Brandão).

Funding

The authors state that they have no funding to declare.

Conflicts of interest

The authors have no conflicts of interest to declare.

Acknowledgments

The authors gratefully acknowledge all centers that participated in the Stent for Life Initiative Portugal between 2011 and 2015.

References
[1]
P.G. Steg, S.K. James, D. Atar, et al.
ESC Guidelines for the management of acute myocardial infarction in patients presenting with ST-segment elevation. The Task Force on the management of ST-segment elevation acute myocardial infarction of the European Society of Cardiology (ESC).
Eur Heart J, 33 (2012), pp. 2569-2619
[2]
P.T. O’Gara, F.G. Kushner, D.D. Ascheim, et al.
2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
[3]
E.C. Keeley, C.L. Grines.
Primary coronary intervention for acute myocardial infarction.
JAMA, 291 (2004), pp. 736-739
[4]
Authors/Task Force members, S. Windecker, P. Kolh, et al.
2014 ESC/EACTS Guidelines on myocardial revascularization: the Task Force on Myocardial Revascularization of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS) Developed with the special contribution of the European Association of Percutaneous Cardiovascular Interventions (EAPCI).
Eur Heart J, 35 (2014), pp. 2541-2619
[5]
J.E. Bray, D. Stub, P. Ngu, et al.
Mass media campaigns’ influence on prehospital behavior for acute coronary syndromes: an evaluation of the Australian Heart Foundation's Warning Signs Campaign.
J Am Heart Assoc, 4 (2015), pp. e001927
[6]
G. De Luca, H. Suryapranata, F. Zijlstra, et al.
Symptom-onset-to-balloon time and mortality in patients with acute myocardial infarction treated by primary angioplasty.
J Am Coll Cardiol, 42 (2003), pp. 991-997
[7]
G. De Luca, H. Suryapranata, J.P. Ottervanger, et al.
Time delay to treatment and mortality in primary angioplasty for acute myocardial infarction: every minute of delay counts.
Circulation, 109 (2004), pp. 1223-1225
[8]
R.L. McNamara, Y. Wang, J. Herrin, et al.
Effect of door-to-balloon time on mortality in patients with ST-segment elevation myocardial infarction.
J Am Coll Cardiol, 47 (2006), pp. 2180-2186
[9]
B.K. Nallamothu, E.H. Bradley, H.M. Krumholz.
Time to treatment in primary percutaneous coronary intervention.
N Engl J Med, 357 (2007), pp. 1631-1638
[10]
E.R. Bates, A.K. Jacobs.
Time to treatment in patients with STEMI.
N Engl J Med, (2013), pp. 889-892
[11]
D.S. Menees, E.D. Peterson, Y. Wang, et al.
Door-to-balloon time and mortality among patients undergoing primary PCI.
N Engl J Med, 369 (2013), pp. 901-909
[12]
A.E. Denktas, H.V. Anderson, J. McCarthy, et al.
Total ischemic time: the correct focus of attention for optimal ST-segment elevation myocardial infarction care.
JACC: Cardiovasc Interv, 4 (2011), pp. 599-604
[13]
S.B. Deutsch, E.L. Krivitsky.
Decreased door to balloon time: better outcome for the patient?.
World J Cardiovasc Dis, 5 (2015), pp. 49-52
[14]
C.J. Terkelsen, J.T. Sorensen, M. Maeng, et al.
System delay and mortality among patients with STEMI treated with primary percutaneous coronary intervention.
[15]
S. Postma, J.-H.E. Dambrink, A.T.M. Gosselink, et al.
The influence of system delay on 30-day and on long-term mortality in patients with anterior versus non-anterior ST-segment elevation myocardial infarction: a cohort study.
Open Hear, 2 (2015),
[16]
S.S. Rathore, J.P. Curtis, J. Chen, et al.
Association of door-to-balloon time and mortality in patients admitted to hospital with ST elevation myocardial infarction: national cohort study.
BMJ, 338 (2009), pp. b1807
[17]
P. Widimsky, J. Fajadet, N. Danchin, et al.
Stent 4 Life targeting PCI at all who will benefit the most: a joint project between EAPCI, Euro-PCR EUCOMED and the ESC Working Group on Acute Cardiac Care.
EuroIntervention, 4 (2009), pp. 555-557
[18]
H. Pereira, F.J. Pinto, R. Calé, et al.
Stent for Life in Portugal: this initiative is here to stay.
Rev Port Cardiol, 33 (2014), pp. 363-370
[19]
J.P. Loh, L.F. Satler, L.K. Pendyala, et al.
Use of emergency medical services expedites in-hospital care processes in patients presenting with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.
Cardiovasc Revasc Med, 15 (2014), pp. 219-225
[20]
S.D. Kristensen, K.G. Laut, J. Fajadet, et al.
Reperfusion therapy for ST elevation acute myocardial infarction 2010/2011: current status in 37 ESC countries.
Eur Heart J, 35 (2014), pp. 1957-1970
[21]
A.S. Jaffe.
Third universal definition of myocardial infarction.
[22]
R Core Team.
R: a language and environment for statistical computing.
R Foundation for Statistical Computing, (2014),
[23]
A. Betriu, M. Masotti.
Comparison of mortality rates in acute myocardial infarction treated by percutaneous coronary intervention versus fibrinolysis.
Am J Cardiol, 95 (2005), pp. 100-101
[24]
P. Widimský, T. Budesinsky, D. Voráč, et al.
Long distance transport for primary angioplasty vs immediate thrombolysis in acute myocardial infarction. Final results of the randomized national multicentre trial-PRAGUE-2.
Eur Heart J, 24 (2003), pp. 94-104
[25]
P.H. Nielsen, M. Maeng, M. Busk, et al.
Primary angioplasty versus fibrinolysis in acute myocardial infarction: long-term follow-up in the Danish acute myocardial infarction 2 trial.
Circulation, 121 (2010), pp. 1484-1491
[26]
D.S. Pinto, P.D. Frederick, A.K. Chakrabarti, et al.
Benefit of transferring ST-segment-elevation myocardial infarction patients for percutaneous coronary intervention compared with administration of onsite fibrinolytic declines as delays increase.
Circulation, 124 (2011), pp. 2512-2521
[27]
M.-J. de Boer, F. Zijlstra.
STEMI time delays: a clinical perspective: editorial comment on the article by Verweij et al.
Neth Hear J, 23 (2015), pp. 415-419
[28]
S. Koul, P. Andell, A. Martinsson, et al.
Delay from first medical contact to primary PCI and all-cause mortality: a nationwide study of patients with ST-elevation myocardial infarction.
J Am Heart Assoc, 3 (2014), pp. 1-8
[29]
R.O. Roswell, B. Greet, P. Parikh, et al.
From door-to-balloon time to contact-to-device time: predictors of achieving target times in patients with ST-elevation myocardial infarction.
Clin Cardiol, 37 (2014), pp. 389-394
[30]
C.J. Terkelsen, E.H. Christiansen, J.T. Sørensen, et al.
Primary PCI as the preferred reperfusion therapy in STEMI: it is a matter of time.
Heart, 95 (2009), pp. 362-369
[31]
L.J. Lambert, K.A. Brown, L.J. Boothroyd, et al.
Transfer of patients with ST-elevation myocardial infarction for primary percutaneous coronary intervention: a province-wide evaluation of door-in to door-out delays at the first hospital.
Circulation, 129 (2014), pp. 2653-2660
[32]
J. Tarkin, A. Malhotra, A. Apps, et al.
Inter-hospital transfer for primary angioplasty: delays are often due to diagnostic uncertainty rather than systems failure and universal time metrics may not be appropriate.
EuroIntervention, 11 (2015), pp. 511-517
[33]
J.C. Blankenship, T.D. Scott, K.A. Skelding, et al.
Door-to-balloon times under 90 min can be routinely achieved for patients transferred for ST-segment elevation myocardial infarction percutaneous coronary intervention in a rural setting.
J Am Coll Cardiol, 57 (2011), pp. 272-279
[34]
H. Pereira, R. Campante Teles, M. Costa, et al.
Trends in primary angioplasty in Portugal from 2002 to 2013 according to the Portuguese National Registry of Interventional Cardiology.
Rev Port Cardiol, 35 (2016), pp. 395-404
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