Patient delay in seeking care for heart attack symptoms: Findings from focus groups conducted in five US regions

被引:127
作者
Finnegan, JR
Meischke, H
Zapka, JG
Leviton, L
Meshack, A
Benjamin-Garner, R
Estabrook, B
Hall, NJ
Schaeffer, S
Smith, C
Weitzman, ER
Raczynski, J
Stone, E
机构
[1] Univ Minnesota, Sch Publ Hlth, Minneapolis, MN 55455 USA
[2] King Cty Dept Emergency Serv, Seattle, WA USA
[3] Univ Massachusetts, Worcester, MA 01605 USA
[4] Robert Wood Johnson Fdn, Princeton, NJ 08540 USA
[5] Univ Texas, Sch Publ Hlth, Houston, TX USA
[6] Harvard Univ, Cambridge, MA 02138 USA
[7] Univ Alabama Birmingham, Birmingham, AL USA
[8] NHLBI, Bethesda, MD 20892 USA
关键词
acute myocardial infarction; heart attack; community trials; community campaigns; focus groups; formative evaluation; emergency medical care;
D O I
10.1006/pmed.2000.0702
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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 multicenter 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 "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. (C) 2000 American Health Foundation and Academic Press.
引用
收藏
页码:205 / 213
页数:9
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