• Background Lack of communication from healthcare providers contributes to the anxiety and distress reported by patients’ families after a patient’s death in the intensive care unit.• Objective To obtain a detailed picture of the experiences of family members during the hospitalization and death of a loved one in the intensive care unit.• Methods A qualitative study with 4 focus groups was used. All eligible family members from 8 intensive care units were contacted by telephone; 8 members agreed to participate.• Results The experiences of the family members resembled a vortex: a downward spiral of prognoses, difficult decisions, feelings of inadequacy, and eventual loss despite the members’ best efforts, and perhaps no good-byes. Communication, or its lack, was a consistent theme. The participants relied on nurses to keep informed about the patients’ condition and reactions. Although some participants were satisfied with this information, they wished for more detailed explanations of procedures and consequences. Those family members who thought that the best possible outcome had been achieved had had a physician available to them, options for treatment presented and discussed, and family decisions honored.• Conclusions Uncertainty about the prognosis of the patient, decisions that families make before a terminal condition, what to expect during dying, and the extent of a patient’s suffering pervade families’ end-of-life experiences in the intensive care unit. Families’ information about the patient is often lacking or inadequate. The best antidote for families’ uncertainty is effective communication.

Objective To describe the association between reported prepregnancy body mass index (BMI) and screening positive for depression.Design Cohort study.Setting Four urban hospitals in Utah, USA.Population Women delivering a term, singleton, live-born infant at one of four urban hospitals in Utah in the period 2005-2007. Methods Women were enrolled immediately postpartum. Demographic, anthropometric, stressors, psychiatric, and medical/ obstetric and family-history data were obtained. Prepregnancy height, weight, and pregnancy weight gain were self-reported. The primary exposure variable, prepregnancy BMI, was calculated. Women were stratified into the six World Health Organization BMI categories (underweight, normal weight, pre-obese, or obese class 1-3).Main outcome measure At 6-8 weeks postpartum, women were screened for depression using the Edinburgh Postnatal Depression Scale (EPDS). The primary outcome measure was a prespecified EPDS score of ‡12.Results Among the 1053 women studied, 14.4% of normal weight women screened positive for postpartum depression. This proportion was greater in women classed as underweight (18.0%, n = 11), pre-obese (18.5%, n = 38), obese class 1 (18.8%, n = 16), obese class 2 (32.4%, n = 11), and obese class 3 (40.0%, n = 8) (P < 0.01). Controlling for demographic, psychological, and medical/obstetric factors, prepregnancy class-2 (aOR 2.87, 95% CI 1.21-6.81) and class-3 (aOR 3.94, 95% CI 1.38-11.23) obesity remained strongly associated with screening positive for postpartum depression, compared with women of normal weight.Conclusions Self-reported prepregnancy obesity may be associated with screening positive for depression when measured postpartum.

BACKGROUND: With much attention being focused on how patients die and whether or not they are provided appropriate care, the care of dying patients in intensive care units must be described and improved. OBJECTIVES: To describe end-of-life care in intensive care units as perceived by critical care nurses who have taken care of dying patients. METHODS: A semistructured interview guide was developed and revised after pretesting in a focus group of faculty clinicians with extensive, recent experience in intensive care. Four focus groups were held with randomly selected nurses from 4 intensive care units in 2 hospitals; participants had 2 years or more of experience and were working half-time or more. Tapes from each focus group were transcribed and reviewed by the investigators before the subsequent group met. Category labels were developed, and topics and themes were determined. RESULTS: "Good" end-of-life care in the intensive care unit was described as ensuring that the patient is as pain-free as possible and that the patient's comfort and dignity are maintained. Involvement of the patient's family is crucial. A clear, accurate prognosis and continuity of care also are important. Switching from curative care to comfort care is awkward. CONCLUSIONS: Disagreement among patients' family members or among caregivers, uncertainty about prognosis, and communication problems further complicate end-of-life care in intensive care units. Changes in the physical environment, education about end-of-life care, staff support, and better communication would improve care of dying patients and their families.

This study examined the experiences of 181 middle‐aged women who, while raising a family, were also primary care providers for an older demented relative. Results indicated that the caregiver burden depended on the context of the caregiving experience, particularly the relative's place of residence. Employment did not alter responsibilities but did affect coping strategies and perceived health of the caregiver.

The traumatic death of a significant person is an underappreciated adverse life event. Unresolved grief from traumatic death is associated with complicated grief (CG) in adulthood and both contribute to and sustain serious mental illness in adulthood. Persons diagnosed with serious mental illness experiencing CG represent vulnerable persons for whom traditional care is therapeutically insufficient, when the trauma of underlying grief is unaddressed. We examined the feasibility and impact of community implementation of Complicated Grief Group Therapy for persons diagnosed with serious mental illness with CG. Program completers showed statistically significant improvement in grief measures and interpersonal wellbeing. KEYWORDSGrief; complicated grief; group therapy; intervention; community-based; trauma BackgroundIn 2019, there were an estimated 51.5 million adults aged 18 years or older in the United States with any mental, emotional, or behavioral disorder. This number represented 20.6% of all U.S. adults (National Survey on Drug Use and Health; Substance Abuse and Mental Health Services Administration, [SAMHSA] 2019). Persons diagnosed with serious mental illness (SMI), those having enduring, life-impairing mood and thought disorders, represent 5.2% of adults in America. This represents an estimated 13.1 million adults aged 18 years or older in the United States with serious mental illness (SMI). This number represented 5.2% of all U.S. adults. By definition, SMI is mental health disorder that causes serious functional impairment. Prevalence of SMI was higher among females (6.5%) than males (3.9%), and younger adults aged 18-25 years had the highest prevalence of SMI (8.6%) compared to adults aged 26-49 years (6.8%) and aged 50 and older (2.9%) (National Survey on Drug

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