Journals / Turkish archives of pediatrics (Online) / 2022 / Cilt: 57 - Sayı: 3

Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic

Pages
335–341
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Urgent action is needed to address the unmet needs of children with rare inherited metabolic disorders, especially those who has significant developmental delays and/or disabilities for this pandemic and possible future crisis.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Crucial information is lacking on unmet needs of children with rare inherited metabolic disorders during the coronavirus disease 2019 pandemic from low- and middle-income countries.
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Key Findings & Data:Materials and Methods: In a cross-sectional observational design, all children with rare inherited metabolic disorders aged 0-18 years followed at Ankara University School of Medicine Department of Pediatrics Pediatric Metabolism Division were recruited and interviewed via phone calls.
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Conclusion & Impact:Urgent action is needed to address the unmet needs of children with rare inherited metabolic disorders, especially those who has significant developmental delays and/or disabilities for this pandemic and possible future crisis.
🔬Design:Research Article
📍Scope:2019 Verileri
⚙️Variables:Domain Parameters

Özet

Objective: Crucial information is lacking on unmet needs of children with rare inherited metabolic disorders during the coronavirus disease 2019 pandemic from low- and middle-income countries. We aimed to identify the unmet needs of children with rare inherited metabolic disorders from Turkey. Materials and Methods: In a cross-sectional observational design, all children with rare inherited metabolic disorders aged 0-18 years followed at Ankara University School of Medicine Department of Pediatrics Pediatric Metabolism Division were recruited and interviewed via phone calls. The Expanded Guide for Monitoring Child Development enabled assessment of unmet needs and environmental context during coronavirus disease 2019 pandemic. Step-wise logistic regression analysis was used to determine independent factors associated with unmet needs. Results: The sample comprised 229 children (54.1% boys) with rare inherited metabolic disorders (36.7% diet-dependent disorders). Most common diagnoses were amino acid metabolism disorders (40.2%). Of all, 29.3% of the mothers reported depression, 25.3% loss of job of family members during the pandemic. All children had unmet needs: at least 73.0% in health care, 96.8% in education, 78.3% in special services/rehabilitation. Having significant developmental delay and/or disability (odds ratio = 2.31, 95% CI: 1.14-4.67) emerged as the only independent factor associated with unmet needs in health care. Conclusion: Children with rare inherited metabolic disorders and their families in Turkey experience unmet needs in many domains during coronavirus disease 2019 pandemic. Urgent action is needed to address the unmet needs of children with rare inherited metabolic disorders, especially those who has significant developmental delays and/or disabilities for this pandemic and possible future crisis.

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Cite This Article

AKIN, E. Ö., EMİNOĞLU, F. T., DOĞULU, N., YEKEDÜZ, M. K., ÖNCÜL, U., AKPINAR, F., HAYRAN, G. (2022). Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic. Turkish archives of pediatrics (Online), Cilt: 57 - Sayı: 3, 335–341. https://ajindex.com/articles/417326

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References (12)

  1. Ghosh A, Schlecht H, Heptinstall LE, et al. Diagnosing childhoodonset inborn errors of metabolism by next-generation sequencing. Arch Dis Child. 2017
  2. 102(11):1019-1029. [CrossRef] 2. Ullah MA, Husseni AM, Mahmood SU. Consanguineous marriages and their detrimental outcomes in Pakistan: an urgent need for appropriate measures. Int J Commun Med Public Health. 2017
  3. 5(1):3. [CrossRef] 3. Hazan G, Hershkovitz E, Staretz-Chacham O. Incidence of inherited metabolic disorders in southern Israel: a comparison between consanguinity and non-consanguinity communities. Orphanet J Rare Dis. 2020
  4. 15(1):331. [CrossRef] 4. Mayer ML, Skinner AC, Slifkin RT. Unmet need for routine and specialty care: data from the National Survey of Children with Special Health Care Needs. Pediatrics. 2004
  5. 113(2):e109-e115. [CrossRef] 5. Newacheck PW, Hughes DC, Hung YY, Wong S, Stoddard JJ. The unmet health needs of America's children. Pediatrics. 2000
  6. 105(4 Pt 2):989-997. [CrossRef] 6. Saudubray JM, Garcia-Cazorla À. Inborn errors of metabolism overview: pathophysiology, manifestations, evaluation, and management. Pediatr Clin North Am. 2018
  7. 65(2):179-208. [CrossRef] 7. Martins AM, Pessoa ALS, Quesada AA, Ribeiro EM. Unmet needs in PKU and the disease impact on the day-to-day lives in Brazil: results from a survey with 228 patients and their caregivers. Mol Genet Metab Rep. 2020
  8. 100624. [CrossRef] 8. Porter KA, O'Neill C, Drake E, et al. Parent experiences of Sanfilippo syndrome impact and unmet treatment needs: a qualitative assessment. Neurol Ther. 2021
  9. 10(1):197-212. [CrossRef] 9. Pelentsov LJ, Fielder AL, Laws TA, Esterman AJ. The supportive care needs of parents with a child with a rare disease: results of an online survey. BMC Fam Pract. 2016
  10. [CrossRef] 10. Lampe C, Dionisi-Vici C, Bellettato CM, et al. The impact of COVID19 on rare metabolic patients and healthcare providers: results from two MetabERN surveys. Orphanet J Rare Dis. 2020
  11. 15(1):341. [CrossRef] 11. Rare Diseases Europe. Available at: https://www.eurordis.org/ content/people-living-rare-disease-were-severely-impacted-du ring-first-covid-19-wave-30-million-people-europe-must-not-b e-forgot Accessed August 10, 2021. 12. Chung CCY, Ng YNC, Jain R, Chung BHY. A thematic study: impact of COVID-19 pandemic on rare disease organizations and patients across ten jurisdictions in the Asia Pacific region. Orphanet J Rare Dis. 2021
  12. 16(1):119. [CrossRef] 13. Elmonem MA, Belanger-Quintana A, Bordugo A, et al. The impact of