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Perceived family impact and coping mechanisms of caregivers of children with nephrotic syndrome

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Abstract

Background

Pediatric chronic disease impacts the affected child and their family structure. There is limited literature investigating the psychosocial impact of nephrotic syndrome on families.

Methods

Caregivers of children with nephrotic syndrome completed two validated surveys: (1) Impact on Family (IOF) that evaluates the family impact (degree to which family is affected by a pediatric chronic illness) and (2) Coping Health Inventory for Parents (CHIP) that examines the coping patterns used by caregivers. Linear regression models were utilized to determine predictors of perceived family impact and coping patterns.

Results

Seventy-five caregivers of a child with nephrotic syndrome completed the surveys. On a scale from low impact to significant impact to very serious impact, results indicated that nephrotic syndrome had a significant impact on families (mean revised IOF total score 33.04 ± 9.38). Families in the steroid-resistant nephrotic syndrome (SRNS) group reported a higher financial impact compared to the steroid-sensitive nephrotic syndrome (SSNS) group (p = 0.03). Families in the frequently relapsing group (FRNS) reported a higher impact on the caregiver’s ability to cope with the child’s condition compared to the SRNS group (p = 0.02). Tacrolimus use was associated with increasing the perceived family impact (β = 4.76, p = 0.046). CHIP scores indicated that caregivers did not cope well with family integration (component I) but coped well with social support (component II) and communication (component III).

Conclusions

Childhood nephrotic syndrome has a significant overall perceived impact on the family, and caregivers did not cope well regarding strengthening their family life. These findings can be used as outcome measures for future intervention studies to find solutions that would decrease the perceived family burden.

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References

  1. Noone DG, Iijima K, Parekh R (2018) Idiopathic nephrotic syndrome in children. Lancet 392:61–74

    Article  PubMed  Google Scholar 

  2. Stone H, Magella B, Bennett MR (2019) The search for biomarkers to aid in diagnosis, differentiation, and prognosis of childhood idiopathic nephrotic syndrome. Front Pediatr 7:404

    Article  PubMed  PubMed Central  Google Scholar 

  3. The primary nephrotic syndrome in children (1981) Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children. J Pediatr 98:561–564

  4. Iijima K, Sako M, Nozu K (2017) Rituximab for nephrotic syndrome in children. Clin Exp Nephrol 21:193–202

    Article  CAS  PubMed  Google Scholar 

  5. Lee JM, Kronbichler A, Shin JI, Oh J (2021) Current understandings in treating children with steroid-resistant nephrotic syndrome. Pediatr Nephrol 36:747–761

    Article  PubMed  Google Scholar 

  6. Carter SA, Mistry S, Fitzpatrick J, Banh T, Hebert D, Langlois V, Pearl RJ, Chanchlani R, Licht CPB, Radhakrishnan S, Brooke J, Reddon M, Levin L, Aitken-Menezes K, Noone D, Parekh RS (2020) Prediction of short- and long-term outcomes in childhood nephrotic syndrome. Kidney Int Rep 5:426–434

    Article  PubMed  Google Scholar 

  7. Roccella M, Leggio L, Parisi L, Turdo G, Testa D (2005) The quality of life in developing age subjects with chronic renal diseases. Minerva Pediatr 57:119–128

    CAS  PubMed  Google Scholar 

  8. Dinleyici M, Çarman KB, Özdemir C, Harmancı K, Eren M, Kirel B, Şimşek E, Yarar C, Duyan Çamurdan A, Şahin Dağlı F (2019) Quality-of-life evaluation of healthy siblings of children with chronic illness. Balkan Med J 37:34–42

    PubMed  PubMed Central  Google Scholar 

  9. Coster WJ, Haley S, Baryza MJ (1994) Functional performance of young children after traumatic brain injury: a 6-month follow-up study. Am J Occup Ther 48:211–218

    Article  CAS  PubMed  Google Scholar 

  10. Zahr LK, Khoury M, Saoud NB (1994) Chronic illness in Lebanese preschoolers: impact of illness and child temperament on the family. Am J Orthopsychiatry 64:396–403

    Article  CAS  PubMed  Google Scholar 

  11. Van Schoors M, De Paepe AL, Lemiere J, Morez A, Norga K, Lambrecht K, Goubert L, Verhofstadt LL (2019) Family adjustment when facing pediatric cancer: the role of parental psychological flexibility, dyadic coping, and network support. Front Psychol 10:2740

    Article  PubMed  PubMed Central  Google Scholar 

  12. Kolk AM, Schipper JL, Hanewald GJ, Casari EF, Fantino AG (2000) The impact-on-family scale: a test of invariance across culture. J Pediatr Psychol 25:323–329

    Article  CAS  PubMed  Google Scholar 

  13. Toledano-Toledano F, Moral de la Rubia J, McCubbin LD, Cauley B, Luna D (2020) Brief version of the coping health inventory for parents (CHIP) among family caregivers of children with chronic diseases. Health Qual Life Outcomes 18:104

    Article  PubMed  PubMed Central  Google Scholar 

  14. Gothwal VK, Bharani S, Reddy SP (2015) Measuring coping in parents of children with disabilities: a Rasch model approach. PLoS One 10:e0118189–e0118189

    Article  PubMed  PubMed Central  Google Scholar 

  15. Kish AM, Newcombe PA, Haslam DM (2018) Working and caring for a child with chronic illness: a review of current literature. Child Care Health Dev 44:343–354

    Article  CAS  PubMed  Google Scholar 

  16. Rovin BH, Adler SG, Barratt J, Bridoux F, Burdge KA, Chan TM, Cook HT, Fervenza FC, Gibson KL, Glassock RJ, Jayne DRW, Jha V, Liew A, Liu ZH, Mejía-Vilet JM, Nester CM, Radhakrishnan J, Rave EM, Reich HN, Ronco P, Sanders JF, Sethi S, Suzuki Y, Tang SCW, Tesar V, Vivarelli M, Wetzels JFM, Lytvyn L, Craig JC, Tunnicliffe DJ, Howell M, Tonelli MA, Cheung M, Earley A, Floege J (2021) Executive summary of the KDIGO 2021 Guideline for the Management of Glomerular Diseases. Kidney Int 100:753–779

    Article  PubMed  Google Scholar 

  17. Stein RE, Riessman CK (1980) The development of an impact-on-family scale: preliminary findings. Med Care 18:465–472

    Article  CAS  PubMed  Google Scholar 

  18. Bek N, Simsek IE, Erel S, Yakut Y, Uygur F (2009) Turkish version of impact on family scale: a study of reliability and validity. Health Qual Life Outcomes 7:4

    Article  PubMed  PubMed Central  Google Scholar 

  19. Su JC, Kemp AS, Varigos GA, Nolan TM (1997) Atopic eczema: its impact on the family and financial cost. Arch Dis Child 76:159–162

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Al Robaee AA (2010) Reliability and validity of the Arabic version of “dermatitis family impact” questionnaire in children with atopic dermatitis. Int J Dermatol 49:1063–1067

    Article  PubMed  Google Scholar 

  21. Almesned S, Al-Akhfash A, Al Mesned A (2013) Social impact on families of children with complex congenital heart disease. Ann Saudi Med 33:140–143

    Article  PubMed  PubMed Central  Google Scholar 

  22. Graham RJ, Rodday AM, Weidner RA, Parsons SK (2016) the impact on family of pediatric chronic respiratory failure in the home. J Pediatr 175:40–46

    Article  PubMed  Google Scholar 

  23. Stein RE, Jessop DJ (2003) The impact on family scale revisited: further psychometric data. J Dev Behav Pediatr 24:9–16

    Article  PubMed  Google Scholar 

  24. Anderson M, Elliott EJ, Zurynski YA (2013) Australian families living with rare disease: experiences of diagnosis, health services use and needs for psychosocial support. Orphanet J Rare Dis 8:22

    Article  PubMed  PubMed Central  Google Scholar 

  25. Zanon RB, Da Silva MA, Filho EJM, Bandeira DR, Dos Santos MA, Halpern R, Bosa CA (2017) Brazilian study of adaptation and psychometric properties of the Coping Health Inventory for Parents. Psicol Reflex Crit 30:10

    Article  PubMed  PubMed Central  Google Scholar 

  26. Almeida AC, Pereira MG (2016) Psychometric properties of the Portuguese version of the Coping Health Inventory for Parents (CHIP) of adolescents with chronic illness. J Pediatr Nurs 31:528–536

    Article  PubMed  Google Scholar 

  27. Aguilar-Vafaie ME (2008) Coping-Health Inventory for Parents: assessing coping among iranian parents in the care of children with cancer and introductory development of an adapted iranian coping-health inventory for parents. Child Health Care 37:237–260

    Article  Google Scholar 

  28. Han HR, Cho EJ, Kim D, Kim J (2009) The report of coping strategies and psychosocial adjustment in Korean mothers of children with cancer. Psychooncology 18:956–964

    Article  PubMed  PubMed Central  Google Scholar 

  29. Patistea E (2005) Description and adequacy of parental coping behaviours in childhood leukaemia. Int J Nurs Stud 42:283–296

    Article  PubMed  Google Scholar 

  30. Natarajan G, Shankaran S, Pappas A, Bann C, Tyson JE, McDonald S, Das A, Hintz S, Vohr B, Higgins R (2014) Functional status at 18 months of age as a predictor of childhood disability after neonatal hypoxic-ischemic encephalopathy. Dev Med Child Neurol 56:1052–1058

    Article  PubMed  PubMed Central  Google Scholar 

  31. Bonner MJ, Hardy KK, Willard VW, Hutchinson KC (2007) Brief report: psychosocial functioning of fathers as primary caregivers of pediatric oncology patients. J Pediatr Psychol 32:851–856

    Article  PubMed  Google Scholar 

  32. Dawes A, Attipoe S, Mittlesteadt J, Glynn P, Rust S, Debs A, Patel AD (2020) Measuring the impact of epilepsy on families. Epilepsy Behav 111:107254

    Article  PubMed  Google Scholar 

  33. Stein RE, Jessop DJ (1984) Does pediatric home care make a difference for children with chronic illness? Findings from the Pediatric Ambulatory Care Treatment Study. Pediatrics 73:845–853

    Article  CAS  PubMed  Google Scholar 

  34. DeWalt DA, Gross HE, Gipson DS, Selewski DT, DeWitt EM, Dampier CD, Hinds PS, Huang IC, Thissen D, Varni JW (2015) PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions. Qual Life Res 24:2195–2208

    Article  PubMed  PubMed Central  Google Scholar 

  35. Selewski DT, Massengill SF, Troost JP, Wickman L, Messer KL, Herreshoff E, Bowers C, Ferris ME, Mahan JD, Greenbaum LA, MacHardy J, Kapur G, Chand DH, Goebel J, Barletta GM, Geary D, Kershaw DB, Pan CG, Gbadegesin R, Hidalgo G, Lane JC, Leiser JD, Song PX, Thissen D, Liu Y, Gross HE, DeWalt DA, Gipson DS (2014) Gaining the Patient Reported Outcomes Measurement Information System (PROMIS) perspective in chronic kidney disease: a Midwest Pediatric Nephrology Consortium study. Pediatr Nephrol 29:2347–2356

    Article  PubMed  PubMed Central  Google Scholar 

  36. Aguilar BA (2017) The efficacy of art therapy in pediatric oncology patients: an integrative literature review. J Pediatr Nurs 36:173–178

    Article  PubMed  Google Scholar 

  37. Albrecht TA, Hoppe R, Winter MA (2022) How caregivers cope and adapt when a family member is diagnosed with a hematologic malignancy: informing supportive care needs. Cancer Nurs. https://doi.org/10.1097/NCC.0000000000001063

    Article  PubMed  Google Scholar 

  38. Belpame N, Kars MC, Deslypere E, Rober P, Van Hecke A, Verhaeghe S (2021) Coping strategies of adolescent and young adult survivors of childhood cancer: a qualitative study. Cancer Nurs 44:E395–E403

    Article  PubMed  Google Scholar 

  39. Lentz R, Benson AB 3rd, Kircher S (2019) Financial toxicity in cancer care: prevalence, causes, consequences, and reduction strategies. J Surg Oncol 120:85–92

    Article  PubMed  Google Scholar 

  40. Shin H, Bartlett R, De Gagne JC (2020) Integrative literature review on psychological distress and coping strategies among survivors of adolescent cancer. Oncol Nurs Forum 47:E131–E148

    Article  PubMed  Google Scholar 

  41. Lashbrook MP, Valery PC, Knott V, Kirshbaum MN, Bernardes CM (2018) Coping strategies used by breast, prostate, and colorectal cancer survivors: a literature review. Cancer Nurs 41:E23–E39

    Article  PubMed  Google Scholar 

  42. Beanlands H, Maione M, Poulton C, Herreshoff E, Hladunewich MA, Hailperin M, Modes MM, An L, Nunes JW, Trachtman H, Nachman P, Gipson DS (2017) Learning to live with nephrotic syndrome: experiences of adult patients and parents of children with nephrotic syndrome. Nephrol Dial Transplant 32:i98–i105

    Article  PubMed  PubMed Central  Google Scholar 

  43. Kim DH, Yoo IY (2004) Relationship between depression and resilience among children with nephrotic syndrome. Taehan Kanho Hakhoe Chi 34:534–540

    PubMed  Google Scholar 

  44. Khorsandi F, Parizad N, Feizi A, Hemmati MaslakPak M (2020) How do parents deal with their children’s chronic kidney disease? A qualitative study for identifying factors related to parent’s adaptation. BMC Nephrol 21:509

    Article  PubMed  PubMed Central  Google Scholar 

  45. Geense WW, van Gaal BGI, Knoll JL, Cornelissen EAM, van Achterberg T (2017) The support needs of parents having a child with a chronic kidney disease: a focus group study. Child Care Health Dev 43:831–838

    Article  CAS  PubMed  Google Scholar 

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JC, JJ, and CS participated in research design, writing of the manuscript, and data analysis. AB, LC, PS, RF, OB, and SG contributed to the research design and writing of the manuscript.

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Correspondence to Christine B. Sethna.

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Cocorpus, J., Jun, J., Basalely, A. et al. Perceived family impact and coping mechanisms of caregivers of children with nephrotic syndrome. Pediatr Nephrol 38, 1177–1185 (2023). https://doi.org/10.1007/s00467-022-05619-w

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  • DOI: https://doi.org/10.1007/s00467-022-05619-w

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