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Factors associated with changes in the quality of life and family functioning scores of primary caregivers of children and young people with primary brain tumors in Karachi, Pakistan : a prospective cohort study

Zahid, Nida (författare)
Uppsala universitet,Internationell barnhälsa och nutrition,Department of Surgery, Aga Khan University, Karachi, Pakistan
Enam, Syed Ather (författare)
Mårtensson, Thomas (författare)
Uppsala universitet,Internationell barnhälsa och nutrition
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Azam, Iqbal (författare)
Mushtaq, Naureen (författare)
Moochhala, Mariya (författare)
Kausar, Faiza (författare)
Hassan, Aneesa (författare)
Kamran Bakhshi, Saqib (författare)
Javed, Farrukh (författare)
Rehman, Lal (författare)
Mughal, Muhammad Nouman (författare)
Altaf, Sadaf (författare)
Kirmani, Salman (författare)
Brown, Nick (författare)
Uppsala universitet,Internationell barnhälsa och nutrition,Department of Pediatrics, Aga Khan University, Karachi, Pakistan
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 (creator_code:org_t)
BioMed Central (BMC), 2024
2024
Engelska.
Ingår i: BMC Pediatrics. - : BioMed Central (BMC). - 1471-2431. ; 24:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BackgroundThere are limited data available, particularly in low- and middle-income countries (LMICs), on the long-term quality of life (QoL) and family functioning of primary caregivers of children and young people (CYPs) affected by primary brain tumors (PBTs). This study aimed to assess the factors associated with the mean change in QoL and family functioning scores of primary caregivers of CYP patients with PBTs 12 months posttreatment.MethodsThis prospective cohort study enrolled CYPs aged 5–21 years with newly diagnosed PBTs and their primary caregivers. The study was carried out between November 2020 and July 2023. The primary caregivers of CYPs were recruited from two major tertiary care centers in Karachi, Pakistan. The primary caregivers QoL were assessed by the Pediatric Quality of Life Inventory (PedsQL) Family Impact Module. The assessment was undertaken by a psychologist at the time of diagnosis and 12 months posttreatment. The data were analyzed with STATA version 12.ResultsForty-eight CYPs with newly diagnosed PBTs and their primary caregivers (46 mothers and 2 fathers) were enrolled. At 12 months posttreatment, 25 (52%) CYPs and their primary caregivers (mothers) were reassessed, and 23 (48%) were lost to follow-up. On multivariable analysis, a significant decrease in mothers’ mean 12-month posttreatment QoL and family functioning scores was associated with CYP having posttreatment seizures (beta= -10.2; 95% CI: -18.4 to -2.0) and with the financial burden associated with the CYP’s illness (beta= -0.3; 95% CI: -0.4 to -0.1). However, in those cases where CYP had higher posttreatment quality of life scores (beta = 0.4; 95% CI = 0.1, 0.6) and posttreatment higher verbal intelligence scores (beta = 0.1; 95% CI = 0.01, 0.3), the mothers’ QoL and family functioning scores were significantly greater.ConclusionWe found a significant decrease in QoL of mothers who had a high financial burden and whose CYP had posttreatment seizures. However, those whose CYPs had higher posttreatment verbal intelligence scores and quality of life scores had significantly greater QoL scores. Identification of the factors that influence primary caregivers QoL has the potential to aid in the development of targeted strategies to alleviate stressors and improve the overall quality of life for primary caregivers and their children who are at high risk.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Public Health, Global Health, Social Medicine and Epidemiology (hsv//eng)

Nyckelord

Quality of life
Family functioning
Primary caregivers
Mothers
Children and young people
Primary brain tumor
Cohort study
Pakistan

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