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1.
Prehosp Emerg Care ; 28(7): 955-960, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38619868

RESUMEN

OBJECTIVE: Current guidelines recommend that patients presenting with ST-elevation myocardial infarction (STEMI) to hospitals not capable of performing primary percutaneous coronary intervention (PCI) be transferred to a PCI-capable hospital if reperfusion can be accomplished within 120 min. Most STEMI patients are accompanied by an advanced care paramedic (ACP, equivalent to EMT-P), nurse, or physician who can manage complications should they arise. In our region, stable STEMI patients are transported by primary care paramedics (PCPs, similar scope of practice to advanced EMT) in cases where a nurse, physician, or ACP paramedic is not available. Our goal was to describe adverse events and need for advanced interventions among initially stable STEMI patients during interfacility transfer by PCPs. METHODS: We reviewed ambulance and hospital records of initially stable STEMI patients (as determined by first set of vital signs documented by paramedics) transferred to a PCI-capable hospital by PCPs between March 1, 2014, and December 31, 2019. We identified whether pre-determined adverse clinical events occurred during the transport as well as the potential need for advanced care interventions not within the PCP scope of practice. Adverse events upon arrival in the PCI lab were also identified. RESULTS: Of 346 STEMI patients transferred, 179 met inclusion criteria. The mean age of included patients was 61 years (SD 12.1) and 74.9% (134/179) were male. Median transport interval was 36 min (IQR 3.0). During transport, 47/179 (26.0%) patients experienced pre-defined adverse events; for 16/47 (34%), one or more adverse events was major. Three patients met criteria for ACP interventions. One patient suffered a cardiac arrest and was promptly resuscitated with defibrillation by the PCPs. CONCLUSIONS: We found PCP-interfacility transport of initially stable STEMI patients was safe and associated with a moderate proportion of adverse events, the majority of which did not require an advanced care intervention. These findings may help decision-making to avoid delays transferring stable patients to PCI-capable centers.


Asunto(s)
Transferencia de Pacientes , Infarto del Miocardio con Elevación del ST , Humanos , Infarto del Miocardio con Elevación del ST/terapia , Masculino , Transferencia de Pacientes/normas , Femenino , Persona de Mediana Edad , Anciano , Estudios Retrospectivos , Atención Primaria de Salud , Auxiliares de Urgencia , Servicios Médicos de Urgencia , Intervención Coronaria Percutánea , Seguridad del Paciente , Técnicos Medios en Salud , Paramédico
2.
J Comp Eff Res ; 6(5): 405-412, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28699780

RESUMEN

AIM: Studies on multiple sclerosis in Saudi Arabia remain scant, particularly studies on the psychological aspects. This study measures severities of depression, anxiety and stress, and compares them to the used disease-modifying treatment. MATERIALS & METHODS: Cross-sectional study using a phone questionnaire targeting 452 Saudi patients with relapsing-remitting multiple sclerosis following in King Khalid University Hospital, King Fahad Medical City or Security Forces Hospital. RESULTS: From 235 patients, 149 used interferons, 58 used fingolimod and 28 used natalizumab. Depression scores were similar among all demographic and drug groups. Interferons versus fingolimod anxiety scores were significantly different (p = 0.035). Stress scores were within normal limits. CONCLUSION: Mild anxiety was higher among interferon users, which could be due to injection anxiety reasons.


Asunto(s)
Ansiedad/etiología , Depresión/etiología , Esclerosis Múltiple Recurrente-Remitente/psicología , Administración Oral , Adulto , Estudios Transversales , Femenino , Clorhidrato de Fingolimod/administración & dosificación , Humanos , Inmunosupresores/administración & dosificación , Inyecciones/efectos adversos , Interferón beta-1a/administración & dosificación , Interferon beta-1b/administración & dosificación , Masculino , Esclerosis Múltiple Recurrente-Remitente/tratamiento farmacológico , Natalizumab/administración & dosificación
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