61 research outputs found

    Anomalous Retinal Correspondence: Diagnostic Tests And Therapy

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    Perinatal palliative care in sub-Saharan Africa: recommendations for practice, future research, and guideline development

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    Worldwide, sub-Saharan Africa has the highest burden of global neonatal mortality (43%) and neonatal mortality rate (NMR): 27 deaths per 1,000 live births. The WHO recognizes palliative care (PC) as an integral, yet underutilized, component of perinatal care for pregnancies at risk of stillbirth or early neonatal death, and for neonates with severe prematurity, birth trauma or congenital anomalies. Despite bearing a disproportionate burden of neonatal mortality, many strategies to care for dying newborns and support their families employed in high-income countries (HICs) are not available in low-and-middle-income countries (LMICs). Many institutions and professional societies in LMICs lack guidelines or recommendations to standardize care, and existing guidelines may have limited adherence due to lack of space, equipment, supplies, trained professionals, and high patient load. In this narrative review, we compare perinatal/neonatal PC in HICs and LMICs in sub-Saharan Africa to identify key areas for future, research-informed, interventions that might be tailored to the local sociocultural contexts and propose actionable recommendations for these resource-deprived environments that may support clinical care and inform future professional guideline development

    Choosing wisely: should past medical decisions impact the allocation of scarce ECMO resources?

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/133548/1/apa13457_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/133548/2/apa13457.pd

    Triage ethics not individual choice

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    Use of composite NICU research outcomes for goals of care counselling creates ethical challenges

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/170945/1/apa16018_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/170945/2/apa16018.pd

    A Tough Decision: Parents’ Perspective on Shared Decision-Making About Tracheostomies

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    Often when patients and families face the decision to pursue a tracheostomy or not, there is not a clear “right answer” as to whether this is in the child’s best interest. These decisions should be instead based on anticipated outcomes and patient/family values around those possible outcomes, and the burden of making these decisions shared between clinicians and patients/parents. Limited decision tools exist, however to support parents and clinicians facing pediatric tracheostomy decisions. This is likely because most patient- or parent-facing decision tools focus on communicating specific information about the options, risks, and outcomes, which differ widely across pediatric conditions. For many of these conditions, no population data exist to guide decision-making. Most the education around shared decision-making has targeted clinicians; relying on the assumption that clinicians will become adept at this and utilize it effectively in practice. Unfortunately, not all clinicians receive or use this training, and evidence shows that patients and families are not well engaged in shared decision-making in practice. To address this gap, we sought to develop a clinical, bedside intervention with peer parent narratives to help parents understand the shared decision making (SDM) process, their role in the decision, and other parents’ considerations in this context. We identified nine parents of eight parents who had faced a tracheostomy decision for their child and were willing to talk about their experiences on a video recording. Half of the parents had chosen tracheostomy; some children of parents making either choice had died. We included parents of diverse racial backgrounds whose children had different diagnoses. Parent interviews, along with an explanation of SDM for parents based on the literature and professional society recommendations, were edited into a 17-minute video guided by iterative feedback from parents and clinicians. This video is intended to complement individualized counseling about the tracheostomy decision and discussions of patients/families goals, values, and preferences.University of Michigan M-Cubed 3.0 Granthttp://deepblue.lib.umich.edu/bitstream/2027.42/192788/1/ToughDecisionAbstract.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/192788/4/PituchEmailCorrespondence.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/192788/5/KukoraEmailCorrespondence.pdfDescription of ToughDecisionAbstract.pdf : AbstractSEL
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