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      The first survey of the Saudi Acute Myocardial Infarction Registry Program: Main results and long-term outcomes (STARS-1 Program)

      research-article
      1 , * , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 1 , 1 , 1 , 1 , 9 , 1 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 4 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50
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          Abstract

          Background

          Prior acute coronary syndrome (ACS) registries in Saudi Arabia might not have accurately described the true demographics and cardiac care of patients with ACS. We aimed to evaluate the clinical characteristics, management, and outcomes of a representative sample of patients with acute myocardial infarction (AMI) in Saudi Arabia.

          Methods

          We conducted a 1-month snap-shot, prospective, multi-center registry study in 50 hospitals from various health care sectors in Saudi Arabia. We followed patients for 1 month and 1 year after hospital discharge. Patients with AMI included those with or without ST-segment elevation (STEMI or NSTEMI, respectively). This program survey will be repeated every 5 years.

          Results

          Between May 2015 and January 2017, we enrolled 2233 patients with ACS (mean age was 56 [standard deviation = 13] years; 55.6% were Saudi citizens, 85.7% were men, and 65.9% had STEMI). Coronary artery disease risk factors were high; 52.7% had diabetes mellitus and 51.2% had hypertension. Emergency Medical Services (EMS) was utilized in only 5.2% of cases. Revascularization for patients with STEMI included thrombolytic therapy (29%), primary percutaneous coronary intervention (PCI); (42.5%), neither (29%), or a pharmaco-invasive approach (3%). Non-Saudis with STEMI were less likely to undergo primary PCI compared to Saudis (35.8% vs. 48.7%; respectively, p <0.001), and women were less likely than men to achieve a door-to-balloon time of <90 min (42% vs. 65%; respectively, p = 0.003). Around half of the patients with NSTEMI did not undergo a coronary angiogram. All-cause mortality rates were 4%, 5.8%, and 8.1%, in-hospital, at 1 month, and at 1 year, respectively. These rates were significantly higher in women than in men.

          Conclusions

          There is an urgent need for primary prevention programs, improving the EMS infrastructure and utilization, and establishing organized ACS network programs. AMI care needs further improvement, particularly for women and non-Saudis.

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          Radial versus femoral access and bivalirudin versus unfractionated heparin in invasively managed patients with acute coronary syndrome (MATRIX): final 1-year results of a multicentre, randomised controlled trial

          The Minimizing Adverse Haemorrhagic Events by Transradial Access Site and Systemic Implementation of Angiox (MATRIX) programme was designed to assess the comparative safety and effectiveness of radial versus femoral access and of bivalirudin versus unfractionated heparin with optional glycoprotein IIb/IIIa inhibitors in patients with the whole spectrum of acute coronary syndrome undergoing invasive management. Here we describe the prespecified final 1-year outcomes of the entire programme.
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            Comparison of thrombolysis followed by broad use of percutaneous coronary intervention with primary percutaneous coronary intervention for ST-segment-elevation acute myocardial infarction: data from the french registry on acute ST-elevation myocardial infarction (FAST-MI).

            Intravenous thrombolysis remains a widely used treatment for ST-elevation myocardial infarction; however, it carries a higher risk of reinfarction than primary PCI (PPCI). There are few data comparing PPCI with thrombolysis followed by routine angiography and PCI. The purpose of the present study was to assess contemporary outcomes in ST-elevation myocardial infarction patients, with specific emphasis on comparing a pharmacoinvasive strategy (thrombolysis followed by routine angiography) with PPCI. This nationwide registry in France included 223 centers and 1714 patients over a 1-month period at the end of 2005, with 1-year follow-up. Sixty percent of the patients underwent reperfusion therapy, 33% with PPCI and 29% with intravenous thrombolysis (18% prehospital). At baseline, the Global Registry of Acute Coronary Events score was similar in thrombolysis and PPCI patients. Time to initiation of reperfusion therapy was significantly shorter in thrombolysis than in PPCI (median 130 versus 300 minutes). After thrombolysis, 96% of patients had coronary angiography, and 84% had subsequent PCI (58% within 24 hours). In-hospital mortality was 4.3% for thrombolysis and 5.0% for PPCI. In patients with thrombolysis, 30-day mortality was 9.2% when PCI was not used and 3.9% when PCI was subsequently performed (4.0% if PCI was performed in the same hospital and 3.3% if performed after transfer to another facility). One-year survival was 94% for thrombolysis and 92% for PPCI (P=0.31). After propensity score matching, 1-year survival was 94% and 93%, respectively. When used early after the onset of symptoms, a pharmacoinvasive strategy that combines thrombolysis with a liberal use of PCI yields early and 1-year survival rates that are comparable to those of PPCI.
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              Characterization of dyspnoea in PLATO study patients treated with ticagrelor or clopidogrel and its association with clinical outcomes.

              AIMS To describe the incidence of dyspnoea and its associations with demographic characteristics and clinical outcomes in patients with acute coronary syndromes (ACS) treated with ticagrelor or clopidogrel in the PLATelet inhibition and patient Outcomes (PLATO) study. METHODS AND RESULTS In the PLATO study, 18 624 patients were randomized to receive either clopidogrel [300-600 mg loading dose (LD), 75 mg daily] or ticagrelor (180 mg LD, 90 mg b.i.d.). The occurrence of reported dyspnoea adverse events (AEs) was analysed in the 18 421 patients who received at least one dose of study medication in relation to demographic characteristics, clinical outcomes and other associations of patients with and without dyspnoea. A total of 1339 ticagrelor-treated patients (14.5%) and 798 clopidogrel-treated patients (8.7%) had a dyspnoea AE following randomization, with respectively 39 (0.4%) and 24 (0.3%) classified as severe in intensity. Excluding dyspnoea AEs occurring after the secondary endpoint of myocardial infarction (MI), the yearly rates of the efficacy endpoints in dyspnoea AE patients in the ticagrelor and clopidogrel groups were: for the primary composite of CV death, MI, and stroke, 8.8 and 10.4% (unadjusted P = 0.25; adjusted P = 0.54); for CV death, 3.1 and 4.8% (unadjusted P = 0.024; adjusted P = 0.18); and for total death 3.7 and 6.2% (unadjusted P = 0.004; adjusted P = 0.06), respectively. CONCLUSIONS Ticagrelor-related dyspnoea is usually mild or moderate in intensity and does not appear to be associated with differences concerning any efficacy or safety outcomes with ticagrelor compared with clopidogrel therapy in ACS patients.
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                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                21 May 2019
                2019
                : 14
                : 5
                : e0216551
                Affiliations
                [1 ] Department of Cardiac Sciences, King Fahad Cardiac Center, College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [2 ] Department of Cardiology, Ministry of National Guard Health Affair, King Saud bin Abdulaziz University for Health Sciences, COM-WR King Abdullah International Medical Research Center, Jeddah, Saudi Arabia
                [3 ] Madinah Cardiac Center, Madinah, Saudi Arabia
                [4 ] Armed Forces Hospitals Southern Region, Khamis Mushayt, Saudi Arabia
                [5 ] King Salman (North West Armed Forces Hospital), Tabuk, Saudi Arabia
                [6 ] Saud AlBabtain Cardiac Center, Dammam, Saudi Arabia
                [7 ] Prince Sultan Cardiac Center, Buraydah City, Saudi Arabia
                [8 ] Ha’il Cardiac Center, Hail, Saudi Arabia
                [9 ] Saudi Heart Association, Riyadh, Saudi Arabia
                [10 ] King Salman Heart Center, King Fahd Medical City, Riyadh, Saudi Arabia
                [11 ] Obeid Specialized Hospital, Riyadh, Saudi Arabia
                [12 ] Security Forces Hospital, Riyadh, Saudi Arabia
                [13 ] Dallah Hospital, Riyadh, Saudi Arabia
                [14 ] Aljazeera Hospital, Riyadh, Saudi Arabia
                [15 ] King Saud Medical City (Riyadh Medical Complex), Riyadh, Saudi Arabia
                [16 ] Alwatani /National Care Hospital, Riyadh, Saudi Arabia
                [17 ] AlFalah Hospital, Riyadh, Saudi Arabia
                [18 ] King Salman Hospital, Riyadh, Saudi Arabia
                [19 ] Imam Abdulrahman Al Faisal Hospital, Riyadh, Saudi Arabia
                [20 ] King Fahad General Hospital–Jeddah, Saudi Arabia
                [21 ] AlNoor Specialist Hospital, Makkah, Saudi Arabia
                [22 ] Security Forces Hospital, Makkah, Saudi Arabia
                [23 ] King Abdulaziz Hospital and Oncology Center, Jeddah, Saudi Arabia
                [24 ] Althager General Hospital, Jeddah, Saudi Arabia
                [25 ] King Abdulaziz Specialist Hospital, AlTaif, Saudi Arabia
                [26 ] AlZahra Hospital, Madinah, Saudi Arabia
                [27 ] Al-Dar Hospital, Madinah, Saudi Arabia
                [28 ] AlMiqat Hospital, Madinah, Saudi Arabia
                [29 ] King Fahad Hospital, Madinah, Saudi Arabia
                [30 ] Ohud Hospital, Madinah, Saudi Arabia
                [31 ] Alansar Hospital, Madinah, Saudi Arabia
                [32 ] Prince Sultan Cardiac Center, AlHofuf /AlHasa, Saudi Arabia
                [33 ] Al Qateef Central Hospital, Al Qateef, Saudi Arabia
                [34 ] Mohammad Dossary Hospital, Alkhobar, Saudi Arabia
                [35 ] King Khalid General Hospital, Hafar Albatin, Saudi Arabia
                [36 ] King Saud Hospital, Unizah, Saudi Arabia
                [37 ] Dr.Sulaiman Alhabib Hospital, Buraydah, Saudi Arabia
                [38 ] Alrass General Hospital, Arrass, Saudi Arabia
                [39 ] Aseer Central Hospital, Abha, Saudi Arabia
                [40 ] AlNamas General Hospital, AlNamas, Saudi Arabia
                [41 ] Khamis Mushayt General Hospital, Khamis Mushayt, Saudi Arabia
                [42 ] King Khalid Civilian Hospital, Tabuk, Saudi Arabia
                [43 ] Arar Cardiac Center (Prince Abdulla bin Abdulaziz bin Musaed Cardiac Center), Arar, Saudi Arabia
                [44 ] Prince Abdulaziz Bin Musaid Hospital, Arar, Saudi Arabia
                [45 ] Prince Sultan Cardiac Center-King Khalid Hospital, Najran, Saudi Arabia
                [46 ] Prince Meteb Ibn Abdulaziz Hospital, Sakaka, Saudi Arabia
                [47 ] King Abdullaziz Specialist Hospital, Sakaka, Saudi Arabia
                [48 ] Dumat AlJandal Hospital, Dumat AlJandal, Saudi Arabia
                [49 ] King Fahd Hospital, AlBaha, Saudi Arabia
                [50 ] King Fahad Central Hospital, Jizan, Saudi Arabia
                Keele University, UNITED KINGDOM
                Author notes

                Competing Interests: Astra Zeneca and Algorithm pharmaceutical companies are the commercial funders of the (STARS-1 Program). This does not alter our adherence to PLOS ONE policies on sharing data and materials.

                Author information
                http://orcid.org/0000-0002-6692-3874
                Article
                PONE-D-18-34207
                10.1371/journal.pone.0216551
                6528983
                31112586
                e104dae8-ccd6-48a1-b76e-eba4977e3189
                © 2019 Alhabib et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 29 November 2018
                : 23 April 2019
                Page count
                Figures: 3, Tables: 2, Pages: 20
                Funding
                Funded by: AstraZeneca (KSA)
                Award Recipient :
                Funded by: Algorithm pharmaceutical company
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100002393, Saudi Heart Association;
                Award Recipient :
                Funded by: Emergency Department Support Program, Ministry of Health
                Award Recipient :
                Funded by: College of Medicine Research Center at King Khalid University Hospital, King Saud University
                Award Recipient :
                This research was funded by AstraZeneca (KSA), Algorithm pharmaceutical company, Saudi Heart Association, Emergency Department Support Program, Ministry of Health, and the College of Medicine Research Center at King Khalid University Hospital, King Saud University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
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