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美国成年先天性心脏病幸存者的吸烟情况:患病率及其与疾病认知的关系。

Smoking among adult congenital heart disease survivors in the United States: Prevalence and relationship with illness perceptions.

作者信息

Fox Kristen R, Hardy Rose Y, Moons Philip, Kovacs Adrienne H, Luyckx Koen, Apers Silke, Cook Stephen C, Veldtman Gruschen, Fernandes Susan M, White Kamila, Kutty Shelby, Jackson Jamie L

机构信息

Center for Biobehavioral Health, Nationwide Children's Hospital, Columbus, OH, USA.

Center for Innovation in Pediatric Practice, Nationwide Children's Hospital, Columbus, OH, USA.

出版信息

J Behav Med. 2021 Dec;44(6):772-783. doi: 10.1007/s10865-021-00239-5. Epub 2021 Jun 29.

Abstract

The relationship between smoking and illness perceptions among congenital heart disease (CHD) survivors is unknown. The primary aims of the present study were to compare the smoking prevalence among CHD survivors to a nationally representative U.S. sample and examine the relationship between smoking and illness perceptions. CHD survivors (N = 744) from six U.S. sites participated in the study. The smoking prevalence among CHD survivors (9.3%) was lower than the general population (15.3%). However, 23.3% of CHD survivors with severe functional limitations smoked. Smoking prevalence differed by U.S. region, with a greater proportion of those attending CHD care in the Midwest reporting smoking (11.8%). The illness perception dimensions of Concern and Emotional Response were independently associated with smoking. Differences in illness perceptions enhance our understanding of smoking among CHD survivors and may guide interventions promoting positive health behaviors. The protocol for the study from which the present analyses were conducted was recorded at ClinicalTrials.gov: NCT02150603.

摘要

先天性心脏病(CHD)幸存者中吸烟与疾病认知之间的关系尚不清楚。本研究的主要目的是将CHD幸存者的吸烟率与具有全国代表性的美国样本进行比较,并研究吸烟与疾病认知之间的关系。来自美国六个地点的744名CHD幸存者参与了该研究。CHD幸存者的吸烟率(9.3%)低于一般人群(15.3%)。然而,23.3%有严重功能受限的CHD幸存者吸烟。吸烟率因美国地区而异,在中西部接受CHD护理的人群中报告吸烟的比例更高(11.8%)。关注和情绪反应的疾病认知维度与吸烟独立相关。疾病认知的差异增进了我们对CHD幸存者吸烟情况的理解,并可能指导促进积极健康行为的干预措施。进行本分析所依据的研究方案已在ClinicalTrials.gov上记录:NCT02150603。

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