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来自HARMONY的基线队列数据,这是一项在全科医疗中进行的关于文化安全的家庭暴力管理的整群随机对照试验。

Baseline cohort data from HARMONY, a cluster randomised controlled trial of culturally safe domestic violence management in general practice.

作者信息

Taft Angela J, Young Felicity, Hegarty Kelsey L, Yelland Jane, Mazza Danielle, Boyle Douglas, Norman Richard, García-Moreno Claudia, Nguyen Cattram, Li Xia, Pokharel Bijaya, Leap Molly Allen, Feder Gene

机构信息

Judith Lumley Centre, La Trobe University, Bundoora, Vic, 3086, Australia.

Department of General Practice and Primary Care, University of Melbourne, Parkville, Australia.

出版信息

BMC Prim Care. 2025 Jul 28;26(1):232. doi: 10.1186/s12875-025-02890-2.

Abstract

BACKGROUND

Domestic violence and abuse (DVA) is a globally prevalent, health damaging problem. In high income countries, migrant /refugee populations from low/middle income countries often consist of young families. DVA is more prevalent, and barriers to disclosure greater among migrant/refugee than native-born families. Consequently, general practice (GP) patient populations are increasingly diverse, but evidence for culturally safe and effective GP management is minimal. The HARMONY study tested a culturally safe DVA intervention to improve GP identification and referral among South Asian families.

METHODS

HARMONY was a pragmatic cluster RCT in 19 GP clinics in two regions of Melbourne, Australia. Eligible practices required ≥ 1 South Asian GP; used one of two common software programs; and agreed to have GrHanite™ software on practice computers. This analysis investigated baseline DVA and ethnicity identification in routine electronic GP data. Deidentified aggregated data for female patients aged ≥ 18 with DVA identification, referral, and South Asian ethnicity data were extracted from medical records. Chi Square for comparison of proportions.

RESULTS

Twenty-four clinics were recruited and randomised, but five dropped out due to Covid. Fifty-two percent (50/96) of 19 clinics' staff were South Asian. While 46.7% of female patients (21,220/45,438) were aged 26-45 years, 17.6% (7,874/45,438) were South Asian. There were more South Asian patients in Comparison 20.6% (4,193/20,312) than Intervention 14.7% (3,681/25,126) clinics. South Asian women had less access to Medicare (83% vs 97%) and pensions (13% vs 22%). At baseline, clinicians recorded 0.58% (265/45,438) DVA-affected women. Notably, they identified fewer South Asian (0.38%) (28/7,874) than non-South Asian women experiencing DVA (0.63%) (237/37,564),-0.28% (0.12%-0.43%), p = 0.004. No referrals were identified.

CONCLUSION

DVA was notably under-identified in these patient populations, but worse among South-Asian female patients. While almost one in six of HARMONY's female population were South Asian, fewer than four in 1000 South Asian women were identified as experiencing DVA. Greater effort to regularly train and to support GP clinics to better identify DVA is vital but even more important in diverse communities to provide culturally safe DVA identification, care and documentation.

TRIAL REGISTRATION

ACTRN12618001845224 on 13/11/2018.

摘要

背景

家庭暴力与虐待(DVA)是一个全球普遍存在且危害健康的问题。在高收入国家,来自低/中等收入国家的移民/难民群体往往以年轻家庭为主。与本地出生的家庭相比,家庭暴力与虐待在移民/难民家庭中更为普遍,且披露障碍更大。因此,全科医疗(GP)的患者群体日益多样化,但关于文化安全且有效的全科医疗管理的证据却很少。和谐研究测试了一种文化安全的家庭暴力与虐待干预措施,以改善南亚家庭中全科医生的识别与转诊情况。

方法

和谐研究是在澳大利亚墨尔本两个地区的19家全科医疗诊所进行的一项实用整群随机对照试验。符合条件的诊所需要有≥1名南亚全科医生;使用两种常见软件程序之一;并同意在诊所电脑上安装GrHanite™软件。本分析调查了常规电子全科医疗数据中的基线家庭暴力与虐待情况及种族识别情况。从病历中提取了年龄≥18岁、有家庭暴力与虐待识别、转诊及南亚种族数据的女性患者的去识别化汇总数据。采用卡方检验比较比例。

结果

招募并随机分配了24家诊所,但有5家因新冠疫情退出。19家诊所中52%(50/96)的工作人员是南亚人。虽然46.7%的女性患者(21,220/45,438)年龄在26 - 45岁之间,但17.6%(7,874/45,438)是南亚人。对照组诊所的南亚患者比例为20.6%(4,193/20,312),高于干预组的14.7%(3,681/25,126)。南亚女性获得医疗保险的比例较低(83%对97%),领取养老金的比例也较低(13%对22%)。在基线时,临床医生记录了0.58%(265/45,438)受家庭暴力与虐待影响的女性。值得注意的是,他们识别出经历家庭暴力与虐待的南亚女性(0.38%)(28/7,874)比非南亚女性(0.63%)(237/37,564)少,差异为 -0.28%(0.12% - 0.43%),p = 0.004。未发现有转诊情况。

结论

在这些患者群体中,家庭暴力与虐待的识别明显不足,在南亚女性患者中情况更糟。虽然和谐研究中近六分之一的女性是南亚人,但每1000名南亚女性中被识别为经历家庭暴力与虐待的不到4人。加大力度定期培训并支持全科医疗诊所更好地识别家庭暴力与虐待至关重要,但在多元化社区中,提供文化安全的家庭暴力与虐待识别、护理及记录更为重要。

试验注册

2018年11月13日,澳大利亚新西兰临床试验注册中心编号ACTRN12618001845224 。

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