Acceptability of dried blood spot collection by primary caregivers of Filipino patients with maple syrup urine disease (MSUD) and phenylketonuria (PKU).

IF 1.5 Q4 GENETICS & HEREDITY
Roxanne Janica E Merencilla, Ebner Bon G Maceda, Jeanne Ruth U Basas, Rufus Thomas Y Adducul, Ma Lourdes Francisco, Justin Von Licudo, Leniza G de Castro-Hamoy
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Abstract

MSUD and PKU require lifetime management hence, regular monitoring of amino acid levels is needed to achieve good metabolic control. Ideally, plasma amino acid analysis (PLAA) is used to monitor concentrations but is expensive and not widely available in local laboratories. The newborn screening program in the Philippines uses dried blood spot (DBS) analysis as an alternative where only trained healthcare providers are allowed to perform the collection at selected facilities. With the increasing number of patients, DBS monitoring has been noted to be delayed due to multiple factors. This issue became even more evident during the COVID-19 pandemic where high-risk patients need to travel outside for blood collection. The study used a cross-sectional study design to determine the primary caregivers' perspective on DBS self-sampling for patients with MSUD and PKU and the acceptability of the samples collected. This was done through a series of collection training, pre-/post- surveys, and 10-item questionnaire, and an in-depth 1-on-1 interview for thematic analysis. The acceptability of samples was processed and evaluated by the newborn screening laboratory. At-home DBS collection by primary caregivers was found to be acceptable. The provision of knowledge and routine collection training by the medical team aids in the increase of sample acceptability as well as a source of empowerment in being equipped to take care of their child. It is highly recommended that DBS samples collected by caregivers be considered acceptable for more time and cost-saving monitoring of the patients' metabolites. This practice also promotes timely and appropriate management which can lead to better patient health outcomes.

菲律宾枫糖尿症(MSUD)和苯丙酮尿症(PKU)患者的主要护理人员对干血斑采集的接受程度。
MSUD 和 PKU 需要终生管理,因此需要定期监测氨基酸水平,以实现良好的代谢控制。理想情况下,血浆氨基酸分析(PLAA)可用于监测氨基酸浓度,但其价格昂贵,而且在当地实验室并不普及。菲律宾的新生儿筛查计划使用干血斑(DBS)分析作为替代方法,只有经过培训的医疗服务提供者才能在选定的机构进行采集。随着患者人数的增加,人们注意到由于多种因素,干血斑监测被延迟了。在 COVID-19 大流行期间,这一问题变得更加明显,因为高危患者需要到户外采血。本研究采用横断面研究设计,以确定主要护理人员对 MSUD 和 PKU 患者 DBS 自我采样的看法以及对所采集样本的接受程度。通过一系列采集培训、事前/事后调查、10 项调查问卷以及 1 对 1 深度访谈进行专题分析。样本的可接受性由新生儿筛查实验室进行处理和评估。结果表明,主要照护者在家中进行 DBS 采集是可以接受的。医疗团队提供的知识和常规采集培训有助于提高样本的可接受性,同时也能增强他们照顾孩子的能力。我们强烈建议将护理人员采集的 DBS 样本视为可接受的样本,以便对患者的代谢物进行更省时省力的监测。这种做法还能促进及时和适当的管理,从而改善患者的健康状况。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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