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1.
Pediatrics ; 144(4)2019 10.
Article in English | MEDLINE | ID: mdl-31484675

ABSTRACT

Doctors are required to notify Child Protective Services (CPS) if parents do not provide appropriate medical care for their children. But criteria for reporting medical neglect are vague. Which treatments properly fall within the realm of shared decision-making in which parents can decide whether to accept doctors' recommendations? Which treatments are so clearly in the child's interest that it would be neglectful to refuse them? When to report medical neglect concerns to CPS may be controversial. It would seem inhumane to allow a child to suffer because of parental refusal to administer proper analgesia. In this ethics rounds, we present a case of an adolescent with chronic pain who is terminally ill. Her parents were not adherent to recommended analgesia regimens. Her palliative care team had to decide whether to report the case to CPS.


Subject(s)
Analgesics, Opioid/therapeutic use , Cancer Pain/drug therapy , Child Abuse , Palliative Care/ethics , Parents , Adolescent , Child Protective Services , Female , Hospices , Humans , Medication Adherence , Personal Autonomy , Self Administration/ethics , Terminally Ill
2.
J Palliat Med ; 22(12): 1506-1514, 2019 12.
Article in English | MEDLINE | ID: mdl-31233350

ABSTRACT

Background: Growing evidence suggests that pediatric palliative care (PPC) teams influence the care received by children and young adults with chronic, life-limiting illnesses. Little is known about how PPC involvement affects advance care planning (ACP) and circumstances of death in pediatric populations with a wide range of diagnoses. Objective: To determine the relationship between PPC involvement, ACP, and circumstances of death for pediatric patients. Design: A retrospective chart review of 558 pediatric patients who died between January 1, 2012 and December 31, 2016 was conducted. Descriptive statistics were used to characterize the sample. A multivariable logistic regression was used to obtain associations between PPC involvement and ACP. Setting: Large, multidisciplinary tertiary care center in a rural state. Measurements: Data abstracted for each patient included the following: demographic information, diagnosis, location of primary unit, hospice involvement, goals of care (GOC), code status, Physician Orders for Life-Sustaining Treatment (POLST) completion, and location of death. Results: Patients with PPC involvement were more likely to have had ACP addressed before death. After adjusting for covariates in the model, patients with PPC were more likely to have their GOC documented (odds ratio [OR] = 96.93), completion of POLST (OR = 24.06), do-not-resuscitate code status (OR = 7.71), and hospice involvement at the time of death (OR = 11.70) compared with those who did not receive PPC. Conclusions: Pediatric patients are more likely to have ACP addressed if they have PPC involvement. Patients with chronic complex conditions are most likely to receive palliative care.


Subject(s)
Advance Care Planning/statistics & numerical data , Cause of Death/trends , Child Mortality/trends , Palliative Care/psychology , Palliative Care/statistics & numerical data , Pediatrics/statistics & numerical data , Referral and Consultation/statistics & numerical data , Adolescent , Child , Child, Preschool , Female , Forecasting , Humans , Infant , Infant, Newborn , Iowa , Logistic Models , Male , Odds Ratio , Retrospective Studies
3.
Pediatrics ; 142(1)2018 07.
Article in English | MEDLINE | ID: mdl-29884681

ABSTRACT

End-of-life care for many infants involves the withdrawal of mechanical ventilation. Usually this takes place in the hospital environment, but sometimes parents request that their infant dies at home. Facilitating this has significant practical and resource implications and raises both logistical and ethical questions. In this article, we report a neonatal case involving home extubation, explaining the processes involved as well as providing an ethical context.


Subject(s)
Airway Extubation/methods , Home Care Services/ethics , Terminal Care/methods , Airway Extubation/ethics , Humans , Infant, Newborn , Male , Terminal Care/ethics
4.
Eur J Immunol ; 36(9): 2535-43, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16897814

ABSTRACT

The activation molecule CD40 and the death receptor CD95/Fas play important roles in regulating B cells so that effective antimicrobial immunity occurs without autoimmunity. CD40 signaling increases CD95 expression, sensitizing cells to apoptosis, but sustained CD40 signals rescue B cells from CD95 killing. Here we describe a mechanism of early CD40-mediated rescue from CD95-induced apoptosis in B cells. Maximal rescue was achieved when CD40 signals were given within 1-2 h of initiating CD95 apoptosis. CD40 signaling did not block association of Fas-associated death domain-containing protein with CD95, but decreased CD95-induced activation of caspases 3 and 8. Rapid CD40 rescue did not require NF-kappaB activation and was independent of de novo protein synthesis, but was dependent upon active PI3 K. Signaling via a CD40 mutant that does not bind TNFR-associated factor (TRAF)1, TRAF2, and TRAF3 rescued B cells from CD95-induced apoptosis. TRAF1/2/3-independent rescue was confirmed in B cell lines made deficient in these TRAF molecules by gene targeting. In contrast, CD40 rescue was completely abrogated in TRAF6-deficient B cells, which showed reduced activation of Akt in response to CD40 engagement. These results reveal a new rapid mechanism to balance B cell activation and apoptosis.


Subject(s)
Apoptosis/immunology , B-Lymphocytes/immunology , CD40 Antigens/immunology , Phosphatidylinositol 3-Kinases/immunology , Receptors, Tumor Necrosis Factor/immunology , fas Receptor/immunology , Animals , B-Lymphocytes/metabolism , CD40 Antigens/metabolism , Caspases/immunology , Cell Line , Enzyme Activation/immunology , Immunoblotting , Immunoprecipitation , Lymphocyte Activation/immunology , Mice , Phosphatidylinositol 3-Kinases/metabolism , Receptors, Tumor Necrosis Factor/metabolism , TNF Receptor-Associated Factor 1/deficiency , TNF Receptor-Associated Factor 1/immunology , TNF Receptor-Associated Factor 2/deficiency , TNF Receptor-Associated Factor 2/immunology , TNF Receptor-Associated Factor 3/deficiency , TNF Receptor-Associated Factor 3/immunology , TNF Receptor-Associated Factor 6/deficiency , TNF Receptor-Associated Factor 6/immunology , fas Receptor/metabolism
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