• Title of article

    Patient Delay in Seeking Care for Heart Attack Symptoms: Findings from Focus Groups Conducted in Five U.S. Regions

  • Author/Authors

    John R. Finnegan Jr.، نويسنده , , Hendrika Meischke، نويسنده , , Jane G. Zapka، نويسنده , , Laura Leviton، نويسنده , , Angela Meshack، نويسنده , , Ruby Benjamin-Garner، نويسنده , , Barbara Estabrook، نويسنده , , Nancy Johnston Hall، نويسنده , , Sheri Schaeffer، نويسنده , , Cassandra Smith، نويسنده , , Elissa R. Weitzman، نويسنده , , James Raczynski، نويسنده , , Elaine Stone، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2000
  • Pages
    9
  • From page
    205
  • To page
    213
  • Abstract
    Background. Patient delay in seeking health care for heart attack symptoms is a continuuing problem in the United States. Methods. Investigators conducted focus groups (N = 34; 207 participants) in major U.S. regions (NE, NW, SE, SW, MW) as formative evaluation to develop a multi-center randomized community trial (the REACT Project). Target groups included adults with previous heart attacks, those at higher risk for heart attack, and bystanders to heart attacks. There were also subgroups reflecting gender and ethnicity (African-American, Hispanic-American, White). Findings. Patients, bystanders, and those at higher risk expected heart attack symptoms to present as often portrayed in the movies, that is, as sharp, crushing chest pain rather than the more common onset of initially ambiguous but gradually increasing discomfort. Patients and those at higher risk also unrealistically judge their personal risk as low, understand little about the benefits of rapid action, are generally unaware of the benefits of using EMS/9-1-1 over alternative transport, and appear to need the “permission” of health care providers or family to act. Moreover, participants reported rarely discussing heart attack symptoms and appropriate responses in advance with health care providers, spouses, or family members. Women often described heart attack as a “male problem,” an important aspect of their underestimation of personal risk. African-American participants were more likely to describe negative feelings about EMS/9-1-1, particularly whether they would be transported to their hospital of choice. Conclusions. Interventions to reduce patient delay need to address expectations about heart attack symptoms, educate about benefits and appropriate actions, and provide legitimacy for taking specific health care-seeking actions. In addition, strategy development must emphasize the role of health care providers in legitimizing the need and importance of taking rapid action in the first place.
  • Keywords
    Focus groups , emergency medical care. , Acute myocardial infarction , Heart attack , Community trials , community campaigns , Formative evaluation
  • Journal title
    Preventive Medicine
  • Serial Year
    2000
  • Journal title
    Preventive Medicine
  • Record number

    803269