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Utilization of Palliative Care for Patients with COVID-19 and Acute Kidney Injury during a COVID-19 Surge
Scherer, Jennifer S; Qian, Yingzhi; Rau, Megan E; Soomro, Qandeel H; Sullivan, Ryan; Linton, Janelle; Zhong, Judy; Chodosh, Joshua; Charytan, David M
BACKGROUND AND OBJECTIVES/OBJECTIVE:AKI is a common complication of coronavirus disease 2019 (COVID-19) and is associated with high mortality. Palliative care, a specialty that supports patients with serious illness, is valuable for these patients but is historically underutilized in AKI. The objectives of this paper are to describe the use of palliative care in patients with AKI and COVID-19 and their subsequent health care utilization. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS/METHODS:We conducted a retrospective analysis of New York University Langone Health electronic health data of COVID-19 hospitalizations between March 2, 2020 and August 25, 2020. Regression models were used to examine characteristics associated with receiving a palliative care consult. RESULTS:=0.002). Despite greater use of palliative care, patients with AKI had a significantly longer length of stay, more intensive care unit admissions, and more use of mechanical ventilation. Those with AKI did have a higher frequency of discharges to inpatient hospice (6% versus 3%) and change in code status (34% versus 7%) than those without AKI. CONCLUSIONS:Palliative care was utilized more frequently for patients with AKI and COVID-19 than historically reported in AKI. Despite high mortality, consultation occurred late in the hospital course and was not associated with reduced initiation of life-sustaining interventions. PODCAST/UNASSIGNED:This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2022_02_24_CJN11030821.mp3.
PMID: 35210281
ISSN: 1555-905x
CID: 5172422
Hearing assessment-The challenges and opportunities of self report [Editorial]
Chodosh, Joshua; Blustein, Jan
PMID: 35006618
ISSN: 1532-5415
CID: 5118422
Perceptions of Treatment Burden Among Caregivers of Elders With Diabetes and Co-morbid Alzheimer's Disease and Related Dementias: A Qualitative Study
Vaughan Dickson, Victoria; Melnyk, Halia; Ferris, Rosie; Leon, Alejandra; Arcila-Mesa, Mauricio; Rapozo, Crystalinda; Chodosh, Joshua; Blaum, Caroline S
Many older adults with diabetes (DM) have co-occurring Alzheimer's Disease (AD) and AD-Related Dementias (ADRD). Complex treatment plans may impose treatment burden for caregivers responsible for day-to-day self-management. The purpose of this qualitative study was to describe caregiver perceptions of treatment burden for people with DM-AD/ADRD. Caregivers (n = 33) of patients with DM-AD/ADRD participated in semi-structured interviews about their caregiver role and perceptions of treatment burden of DM-AD/ADRD management. Qualitative data were analyzed using content analysis (ATLAS.ti). Caregivers reported high levels of burden related to complex treatment/self-management for patients with DM-AD/ADRD that varied day-to-day with the patient's cognitive status. Four themes were: (1) trajectory of treatment burden; (2) navigating multiple healthcare providers/systems of care; (3) caregiver role conflict; and (4) emotional burden. Interventions to reduce caregiver treatment burden should include activating supportive services, education, and care coordination especially, if patient treatment increases in complexity over time.
PMID: 34991360
ISSN: 1552-3799
CID: 5107342
Screening for Cognitive Impairment in the Emergency Department [Meeting Abstract]
Asato, C; Ferris, R; Messina, F; Grudzen, C; Fowler, N R; Chodosh, J
Background: Clinical trials are important to improve evidencebased care for persons living with dementia (PLWD) and for their care partners (dyads). Barriers to research recruitment are numerous, including care partners concerns' of ill health, cognitive impairment (CI) severity, and denial of need. The aim of this study is to determine whether a performance- or informant-based screening test for CI is associated with trial enrollment and whether mode of administration influences one's decision to participate.
Method(s): We used cross-sectional data from patients and caregivers who visited the EDs of New York University (NYU) and Indianapolis University (IU) during screening for the Program of Intensive Support in Emergency Departments (ED) for Care Partners of Cognitively Impaired Patients (POISED), which is testing a care management intervention. We offered CI screening to patients >75 years using the Mini-Cog and if unable to do this, we offered their care partners the Short Portable Informant Questionnaire of Cognitive Decline (IQ-CODE). We used chi-square tests and logistic regression to determine whether likelihood of enrollment differed between screening tests and mode of administration: in-person versus telephone.
Result(s): We screened 8860 patients or care partners (dyads) between 3/3/2018-4/1/2021, of which n=2840 at NYU and n=660 at IU had positive screens. Of these 3500 dyads, 2142 had a positive Mini-Cog (<2) and 1358 had a positive IQ-CODE (>3.40). We enrolled 13.9% (n=297) of positive Mini-Cogs and 14.5% (n=309) of positive in-person IQ-CODEs. During the pandemic we conducted all IQCODEs by phone and enrolled 34% (n=196) of those who screened positive. Adjusting for age, sex, and gender, compared to Mini-Cog screening, only those having positive IQCODES by phone were more likely to enroll (adjusted odds ratio (AOR): 3.75 (95% CI: 2.76, 5.11).
Conclusion(s): Higher enrollment using informant-based telephone screening after discharge suggests that care partner recognition of a problem and perhaps having less distraction from the ED visit may increase trial enrollment. Whether the pandemic was the predomant factor encouraging enrollment is unknown
EMBASE:637954158
ISSN: 1531-5487
CID: 5252462
Impact of Neighborhood Deprivation on Persons Living with Dementia and Diabetes [Meeting Abstract]
Oser, M; Ferris, R; Arcila-Mesa, M; Rapozo, C; Chodosh, J
Background: Neighborhood disadvantage influences health outcomes regardless of personal economic status, illustrating the importance of neighborhood context on health. The Area Deprivation index (ADI) establishes a ranking system of U.S. neighborhoods on state and national levels based on 17 neighborhood factors. Using data from an ongoing study of patients with dual diagnoses of diabetes and dementia, we investigated the relationship between ADI and diabetic outcomes, including glycemic control, blood pressure, and dementia severity.
Method(s): We conducted descriptive and bivariate statistics using 3 years of health record data from patients of NYU Langone Health. We included patients >=65 years, with ADRD and DM, and on DM medication. In addition to demographic measures and NY home addresses, we collected hemoglobin A1c, blood pressure, and assessed dementia severity, surveying proxies with the dementia severity rating scale (DSRS). We used ArcGIS and ADI data to link patient addresses to an ADI score. We stratified the sample into two groups: a low deprivation group with ADI scores 1-5, and a high deprivation group with ADI scores 6-10.
Result(s): Of those meeting inclusion criteria (n=996), most were over 75 years (73.5%), female (60.1%), white (71.2%), and not Hispanic or Latino (72.4%). Mean patient age was 81.3; standard deviation (SD): 7.6. More than 50% of patients had an NY state ADI score of 1, 2 or 3 out of 10, indicating that the majority of the population lived in neighborhoods of less disadvantage. 83.4% (n=831) of the population fell into the low deprivation group. There were no differences in hemoglobin A1c (7.09 vs. 7.01) or dementia severity (25.5 +/- 0.8 vs. 22.4 +/- 2.0) between low and high deprivation groups, respectively. However, systolic blood pressure was greater in high deprivation individuals (132.4 +/- 19.3 mm Hg vs. 128.6 +/- 18.2; p=0.02).
Conclusion(s): The ADI in this study was associated with blood pressure but not diabetic control or dementia severity. Less heterogeneity in disadvantage limited our ability to detect this potential social determinant of health. In a city, where neighborhood disadvantage changes from block to block, the influence of environment on health may be more difficult to detect
EMBASE:637954382
ISSN: 1531-5487
CID: 5252412
Outcomes of 4Ms Assessments during Early Phase of Adoption at an Urban Safety Net Primary Care Geriatrics Clinic [Meeting Abstract]
Khanna, P; Nemytova, E; Ajmal, S; Wallach, A B; Chodosh, J; Ouedraogo, Tall S
Background: We recently implemented the Age-Friendly Health System's 4Ms (What Matters, Medication, Mentation, and Mobility) framework in New York City Health + Hospitals/Bellevue Hospital Center's Geriatrics clinic to improve care of older adults.
Method(s): We examined the impact of 4Ms assessment on patient care and changes in care processes through specific interventions triggered after assessment. We conducted chart reviews of patient visits during March 2021, the first month of 4Ms implementation and identified interventions made during these visits. To assess "What Matters" providers asked "What Matters the most to you;" potentially inappropriate Medications (PIM) were identified using the Beers list; Mentation was evaluated using the Mini-Cog; and Mobility was determined using timed up and go (TUG) test. We used descriptive statistics to characterize findings.
Result(s): Among the 121 patients who had 4Ms assessment in March 2021, 85% (n=103) were asked "What Matters;" providers reviewed Medications for almost all (n=118; 98%) and conducted a Mini-Cog for 64% (n=78). Most not cognitively assessed were either previously screened (n=11; 9%) or had dementia (n=12; 10%). Providers used the TUG test for 87% (n=105). What Mattered to patients most commonly was "getting better" (n=24; 23%). There were 39 (33%) patients with potentially inappropriate Medications (including proton pump inhibitors, gabapentinoids, and NSAIDS) of which 10 (26%) Medications were either discontinued or reduced. Other interventions included further cognitive evaluation (n=2) and home care referrals (n=2) among 14 (18%) with an abnormal Mini- Cog. Among the 51 (42%) patients with an abnormal TUG, providers intervened for 19 (37%) with devices, referrals or home services.
Conclusion(s): The adoption of 4Ms assessment during routine visits identified issues with Medications, Mentation and Mobility, triggering several interventions for common geriatric conditions. 4Ms assessment is a helpful strategy to organize geriatric care, routinely assess patients for common geriatric syndromes, and improve care. Future directions include prioritizing interventions integrated with "What Matters" to maintain patient-centered care
EMBASE:637954694
ISSN: 1531-5487
CID: 5252382
A Pilot Randomized Controlled Trial of Integrated Palliative Care and Nephology Care [Meeting Abstract]
Scherer, Jennifer; Rau, Megan; Krieger, Anna; Xia, Yuhe; Brody, Abraham; Zhong, Hua; Charytan, David; Chodosh, Joshua
ISI:000802790300134
ISSN: 0885-3924
CID: 5246832
The impact of a Friendly Telephone Calls program on visits with physicians during pandemic [Letter]
Blachman, Nina L; Lee, Yi Shan; Arcila-Mesa, Mauricio; Ferris, Rosie; Chodosh, Joshua
PMCID:8447359
PMID: 34337742
ISSN: 1532-5415
CID: 5107692
Longitudinal, Interdisciplinary Home Visits vs. Usual Care for Homebound People with Advanced Parkinson's Disease (IN-HOME-PD): Study protocol for a controlled trial
Fleisher, Jori; Hess, Serena; Sennott, Brianna; Myrick, Erica; Wallace, Ellen Klostermann; Lee, Jeanette; Sanghvi, Maya; Woo, Katheryn; Ouyang, Bichun; Wilkinson, Jayne; Beck, James; Johnson, Tricia; Hall, Deborah; Chodosh, Joshua
BACKGROUND:Current understanding of advanced Parkinson's disease (PD) and its treatment is largely based on data from outpatient visits. The most advanced and disabled individuals become disconnected from both care and research. A previous pilot study among older, multimorbid patients with advanced PD demonstrated the feasibility of interdisciplinary home visits to reach the target population, improve care quality, and potentially avoid institutionalization. OBJECTIVE:The following protocol tests whether interdisciplinary home visits can 1) prevent decline in quality of life and 2) prevent worsening caregiver strain. Finally, the protocol explores whether program costs are offset by savings in healthcare use and institutionalization when compared with usual care. METHODS:In this single-center, controlled trial, 65 patient-caregiver dyads affected by advanced PD (Hoehn & Yahr stages 3-5 and homebound) are recruited to receive quarterly interdisciplinary home visits over one year. The one-year intervention is delivered by a nurse and research coordinator who travel to the home supported by a movement disorders specialist and social worker (both present by video). Each dyad is compared with age-, sex-, and Hoehn and Yahr stage-matched control dyads drawn from US participants in the longitudinal Parkinson's Outcome Project registry. The primary outcome measure is change in patient quality of life between baseline and one year. Secondary outcome measures include change in Hoehn & Yahr stage, caregiver strain, self-reported fall frequency, emergency room visits, hospital admissions, and time-to-institutionalization and/or death. Intervention costs and changes in healthcare utilization will be analyzed in a budget impact analysis exploring the potential for model adaptation and dissemination. RESULTS:The protocol was funded in September 2017 and approved by the Rush Institutional Review Board in October 2017. Recruitment began in May 2018 and closed in November 2019 with 65 patient-caregiver dyads enrolled. All study visits have been completed and analysis is underway. CONCLUSIONS:To our knowledge, this is the first controlled trial to investigate the effects of interdisciplinary home visits among homebound individuals with advanced Parkinson's disease and their caregivers. This study also establishes a unique cohort of patients from whom we can study the natural course of advanced PD, its treatments, and unmet needs. CLINICALTRIAL/UNASSIGNED:Clinicaltrials.gov, NCT03189459.
PMID: 34238753
ISSN: 1929-0748
CID: 4933512
Hospital volunteers: an innovative pipeline to increase the geriatrics workforce
Sun, H; Zweig, Y; Perskin, M; Chodosh, J; Blachman, N L
PMID: 34229562
ISSN: 1545-3847
CID: 4951042