Crain E F, Kercsmar C, Weiss K B, Mitchell H, Lynn H
Department of Pediatrics, Albert Einstein College of Medicine, Jacobi Medical Center, Bronx, NY 10461, USA.
Arch Pediatr Adolesc Med. 1998 Apr;152(4):333-9. doi: 10.1001/archpedi.152.4.333.
To characterize perceived access and barriers to quality health care for asthma among the caregivers of children in the inner city.
Multicenter, cross-sectional survey.
Eight sites in 7 major metropolitan US inner cities.
A systematic sample of children with asthma, aged 4 to 9 years, and their caregivers who resided in census tracts in which at least 30% of the households were below the 1990 federal poverty guidelines, recruited from 25 primary care clinics and 13 emergency departments (EDs) from November 1, 1992, through October 31, 1993.
Of the 1528 children enrolled, 1376 had physician-diagnosed asthma and form the basis of this report. This group was further divided into 284 children (20.6%) who met all recruitment criteria for severe asthma and 207 (15.0%) with mild asthma who met none. Of parents in the total sample, 95.6% reported a usual place for short-term asthma care for their child; 75.4% used the ED. Children with severe asthma were significantly more likely to use the ED than those with mild asthma (84.3% vs 63.0%; P<.01). A usual place for follow-up asthma care was reported by 96.7% of subjects. There were no differences in access or type of facility used by asthma severity. More than half the study group reported difficulty in accessing care for acute asthma attacks and for follow-up care with no differences by asthma severity. Among those with severe asthma, 47.5% used inhaled steroids or cromolyn, 52.8% used a spacer device if they had been prescribed a metered dose inhaler, and 21.2% of children older than 6 years were prescribed a peak flowmeter. Patients with mild asthma were significantly less likely to report use of all 3 items (steroids or cromolyn, 1.4%; spacer device, 15.4%; and peak flowmeter, 3.1%, respectively; P<.01).
Although access to asthma care among children in US inner cities appears adequate as determined by the traditional measure of reporting a regular source of care, barriers are frequently reported, as are deficiencies in the quality of medical care.
描述美国市中心区儿童看护者对哮喘优质医疗服务的可及性认知及障碍。
多中心横断面调查。
美国7个主要大都市市中心区的8个地点。
从1992年11月1日至1993年10月31日,从25家初级保健诊所和13家急诊科招募的4至9岁哮喘儿童及其看护者的系统样本,这些儿童居住在普查区,其中至少30%的家庭低于1990年联邦贫困线标准。
在1528名登记儿童中,1376名有医生诊断的哮喘,构成本报告的基础。该组进一步分为符合重度哮喘所有招募标准的284名儿童(20.6%)和不符合任何标准的轻度哮喘儿童207名(15.0%)。在总样本中的家长中,95.6%报告孩子有一个常规的短期哮喘护理场所;75.4%使用急诊科。重度哮喘儿童比轻度哮喘儿童更有可能使用急诊科(84.3%对63.0%;P<0.01)。96.7%的受试者报告有哮喘后续护理的常规场所。哮喘严重程度在医疗服务可及性或使用的机构类型方面没有差异。超过一半的研究组报告在获得急性哮喘发作护理和后续护理方面存在困难,且哮喘严重程度之间没有差异。在重度哮喘患者中,47.5%使用吸入性类固醇或色甘酸钠,52.8%在使用定量吸入器时使用储雾罐,6岁以上儿童中有21.2%被开了峰流速仪。轻度哮喘患者报告使用所有三项(类固醇或色甘酸钠、储雾罐、峰流速仪)的可能性显著更低(分别为1.4%、15.4%和3.1%;P<0.01)。
尽管根据报告常规护理来源这一传统指标判断,美国市中心区儿童获得哮喘护理的情况似乎足够,但经常报告存在障碍,医疗服务质量也存在不足。