Lock J, Raat H, Peters M, Scholten M, Beijlevelt M, Oostenbrink R, Leebeek F W G, Moll H A, Cnossen M H
Department of Paediatric Haematology, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands.
Department of Public Health, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Haemophilia. 2016 Nov;22(6):841-851. doi: 10.1111/hae.13043. Epub 2016 Oct 25.
Transmural support by a haemophilia nurse may improve treatment and may empower parents and patients.
To measure the effect of structured home visits by a haemophilia nurse in (parents of) patient on aspects of prophylactic home treatment.
A multicentre intervention study in two paediatric haemophilia treatment centres was performed. Primary outcome measures were: adherence to prescribed treatment, health-related quality of life and behavioural scores. Secondary outcome measures were: total clotting factor consumption, self-efficacy and number of joint bleeds.
Over a period of 22 months (median, IQR 21-23), four to seven home visits in 46 patients (mean age 9.4 ± 4.2 years) were made. No difference in adherence to prescribed treatment was seen after the home visits when compared to baseline measurements. Both the Child Health Questionnaire (CHQ) scales on 'Role functioning - Emotional/Behavioural' (P = 0.02, d = 0.53) and 'Parental Time Impact' (P = 0.04, d = 0.33) were reduced after intervention. The disease-specific Haemo-QoL questionnaire showed improvement in domains: 'Family' (P = 0.04, d = -0.14), 'Friends' (P = 0.03, d = -0.29) and 'Perceived support' (P = 0.03, d = -0.37). Significant improvement was observed with regard to domain 'Communication' of the VERITAS-Pro scale (P = 0.03, d = -0.28).
After a period of transmural care by a haemophilia nurse, significant but small positive effects were demonstrated with regard to communication and increase of perceived support between parents and haemophilia treatment centre. No improvement was observed in other outcome measures.
血友病护士提供的跨部门支持可能会改善治疗效果,并增强家长和患者的能力。
评估血友病护士进行的结构化家访对患者(家长)预防性家庭治疗各方面的影响。
在两个儿科血友病治疗中心开展了一项多中心干预研究。主要结局指标为:对规定治疗的依从性、健康相关生活质量和行为评分。次要结局指标为:凝血因子总消耗量、自我效能感和关节出血次数。
在22个月(中位数,四分位间距21 - 23个月)的时间里,对46例患者(平均年龄9.4 ± 4.2岁)进行了4至7次家访。与基线测量相比,家访后在规定治疗的依从性方面未观察到差异。干预后,儿童健康问卷(CHQ)中“角色功能 - 情绪/行为”量表(P = 0.02,效应量d = 0.53)和“父母时间影响”量表(P = 0.04,效应量d = 0.33)得分均有所降低。特定疾病的血友病生活质量问卷显示在“家庭”(P = 0.04,效应量d = -0.14)、“朋友”(P = 0.03,效应量d = -0.29)和“感知支持”(P = 0.03,效应量d = -0.37)等领域有所改善。VERITAS - Pro量表的“沟通”领域有显著改善(P = 0.03,效应量d = -0.28)。
经过血友病护士一段时间的跨部门护理后,在家长与血友病治疗中心之间的沟通以及感知支持增加方面显示出显著但较小的积极效果。在其他结局指标方面未观察到改善。