Objective: The sudden cardiac death (SCD) of a young person is a devastating event for any parent. Inherited heart disease is often either identified or assumed to be the cause. Few studies have explored the psychosocial impact to the surviving at-risk family members. We sought to investigate the needs of parents who have experienced the SCD of their child (≤45 years).
Methods: A quantitative needs analysis questionnaire was developed based on semistructured interviews, including one focus group and a review of relevant literature. Eligible participants were invited to participate in this cross-sectional survey study.
Results: There were 38 parents who completed a quantitative survey. Parents' perceived needs for information and support spanned medical, psychosocial, spiritual and financial domains. Of the support and information needs assessed, medical needs were identified as the most important domain, followed by psychosocial, spiritual and financial. Importantly, psychosocial information and support needs were reported as the most unmet need, endorsed by 54% of parents. Medical information and support needs were reported as unmet by almost one third of parents. The two most endorsed needs were 'To have the option of whether or not you would pursue genetic testing for yourself or family members' and 'To understand what happened'.
Conclusions: This work demonstrates for the first time, the multifactorial needs of parents after SCD in the young. With the greatest unmet need reported as psychosocial needs, there is clear necessity to find ways of integrating psychological support in to the care of families after SCD in the young.
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http://dx.doi.org/10.1136/openhrt-2019-001120 | DOI Listing |
Purpose: To investigate the association of local ciliary body morphology with the haptic position and peripheral vault.
Methods: This retrospective observational study included 95 eyes of 59 patients treated with the EVO Implantable Collamer Lens (ICL) (STAAR Surgical). Ciliary body morphology parameters (ciliary process length [CPL], ciliary sulcus width [CSW], and scleral spur-ciliary process distance [SCD]), the relative position of ICL haptic to the ciliary process, the haptic-related parameters (the final tip point of ICL haptic [ftICL haptic] and lowest point of ICL haptic), and peripheral vault in the location of each haptic were measured with ultrasound biomicroscopy 3 months after surgery.
BMC Public Health
March 2025
Uganda Sickle Cell Rescue Foundation, Kampala, Uganda.
Background: Sickle cell disease (SCD) is a debilitating hereditary medical condition associated with pain, stigma, morbidity, and early death. To reduce the prevalence and improve the quality of life of persons with SCD, improved knowledge, practices and reduced stigma are key for Uganda since improved medical breakthroughs in SCD diagnosis, care, and management are expensive in Uganda. However, there is limited research on knowledge, attitudes, and practice (KAP) towards SCD, therefore this study presents the levels and determinants of SCD KAP in Alebtong district, Lango region in Northern Uganda.
View Article and Find Full Text PDFJAMA Health Forum
March 2025
UCSF School of Medicine, UCSF Benioff Children's Hospital, Oakland, California.
Importance: Hemoglobin disorders are a considerable public health issue with more than 500 000 affected infants born annually worldwide. First introduced in the 1970s, newborn screening (NBS) for sickle cell disease (SCD) was included in the Recommended Uniform Screening Panel (RUSP) in 2006, a successful public health promotion and prevention practice that has led to improved childhood survival. Although SCD is the primary target, the screening process also detects many other hemoglobinopathies.
View Article and Find Full Text PDFBMC Psychiatry
March 2025
Tianjin International Joint Research Center for Neural Engineering, Academy of Medical Engineering and Translational Medicine, Tianjin University, No.92 Weijin Road, Nankai District, Tianjin, 300072, China.
Background: Subclinical depression (ScD), serving as a significant precursor to depression, is a prevalent condition in college students and imposes a substantial health service burden. However, the brain network topology of ScD remains poorly understood, impeding our comprehension of the neuropathology underlying ScD.
Methods: Functional networks of individuals with ScD (n = 26) and healthy controls (HCs) (n = 33) were constructed based on functional magnetic resonance imaging data.
PLoS One
March 2025
School of Medicine, College of Health Sciences, Makerere University, Kampala, Uganda.
Background: Sickle Cell Disease (SCD) poses a substantial public health challenge in Uganda, exhibiting distinct regional variations in prevalence. The Uganda Sickle Cell Surveillance Study has estimated an overall SCD prevalence of 13.3%.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!