Chandran Vishnu, Madi Deepak, Chowta Nithyananda, Ramapuram John, Bhaskaran Unnikrishnan, Achappa Basavaprabhu, Jose Hyma
Junior Resident, Department of Medicine, KMC Mangalore, Manipal University , Karnataka, India .
Associate Professor, Department of Medicine, KMC Mangalore, Manipal University , Karnataka, India .
J Clin Diagn Res. 2016 May;10(5):OC41-3. doi: 10.7860/JCDR/2016/20076.7865. Epub 2016 May 1.
In India, family caregivers provide bulk of care to People Living With HIV/AIDS (PLWHA). Caregiver burden refers to the physical, emotional and financial hardships associated with providing care to a diseased individual. Attending to the needs of PLWHA can place a significant burden on family members. This may adversely affect their Quality of Life (QOL).
The main aim of our study was to assess the caregiver burden and QOL among the family members of PLWHA in Southern India. We also determined the impact of caregiver burden on QOL.
This facility based cross-sectional study was carried out at Kasturba Medical College (KMC) Mangalore. The study was conducted over a period of 18 months starting from October 2013. A total of 360 caregivers participated in our study. The data were collected by face-to-face interview. Caregiver burden was assessed using the Zarit Burden scale & WHOQOL-BREF scale was used to assess the QOL of caregivers. The collected data was entered and analysed using SPSS version 11.5. A p-value of less than 0.05 was considered statistically significant.
The mean age of caregivers was 36.09± 10.18 years. Most of the caregivers were females 279 (77.5%). Majority of caregivers 184 (51.1%) belonged to Middle/Lower Middle socioeconomic class (Kuppuswamy class III). Majority of PLWHA 155 (43.1%) had Stage 2 disease. Mean CD4 count of the patients was 405.2± 240 cells/μL. In our study 88(24.4%) caregivers had moderate to severe burden and 36(10%) had very severe burden. Physical domain of QOL showed maximum score of 60.28±13.08, while a minimum score of 51.88 ± 14.20 was seen in social domain. With increase in caregiver burden, the mean QOL scores decreased which was statistically significant.
Our study highlights the need to counsel the caregivers on how to deal with PLWHA in the family. Family care plays a major role in the general wellbeing of PLWHA. Majority of national HIV programmes all over the world focus mainly on PLWHA. National programmes should immediately address the mental health issues of caregivers thereby reducing caregiver burden. More studies on this topic have to be conducted in developing countries.
在印度,家庭照顾者为感染艾滋病毒/艾滋病的患者(PLWHA)提供了大部分护理。照顾者负担指的是与照顾患病个体相关的身体、情感和经济困难。满足PLWHA的需求可能会给家庭成员带来巨大负担。这可能会对他们的生活质量(QOL)产生不利影响。
我们研究的主要目的是评估印度南部PLWHA家庭成员的照顾者负担和生活质量。我们还确定了照顾者负担对生活质量的影响。
这项基于机构的横断面研究在芒格洛尔的卡斯图尔巴医学院(KMC)进行。该研究从2013年10月开始,为期18个月。共有360名照顾者参与了我们的研究。数据通过面对面访谈收集。使用Zarit负担量表评估照顾者负担,使用WHOQOL - BREF量表评估照顾者的生活质量。收集的数据使用SPSS 11.5版本进行录入和分析。p值小于0.05被认为具有统计学意义。
照顾者的平均年龄为36.09±10.18岁。大多数照顾者为女性,共279人(77.5%)。大多数照顾者184人(51.1%)属于中/中低社会经济阶层(库普苏瓦米三世阶层)。大多数PLWHA 155人(43.1%)处于疾病2期。患者的平均CD4细胞计数为405.2±240个/μL。在我们的研究中,88名(24.4%)照顾者有中度至重度负担,36名(10%)有极重度负担。生活质量的身体领域得分最高,为60.28±13.08,而社会领域得分最低,为51.88±14.20。随着照顾者负担的增加,平均生活质量得分下降,这具有统计学意义。
我们的研究强调了需要就如何在家中照顾PLWHA向照顾者提供咨询。家庭护理在PLWHA的总体健康中起着重要作用。全世界大多数国家的艾滋病毒项目主要关注PLWHA。国家项目应立即解决照顾者的心理健康问题,从而减轻照顾者负担。在发展中国家需要对此主题进行更多研究。