Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
1.
Health Promot Pract ; 24(1_suppl): 112S-115S, 2023 05.
Article in English | MEDLINE | ID: mdl-36999496

ABSTRACT

Although food pantries play a key role in addressing food insecurity across the United States, the usual methods of getting food to people in need were severely challenged during the COVID-19 crisis. Chronic disease, lack of transportation, and food insecurity are social determinants that amplify health disparities at higher rates among racial and ethnic minorities throughout the greater Charlotte, North Carolina, area. Loaves & Fishes, a local network of food pantries, partnered with RAO Community Health to develop and support the sustainability of the Specialty Box Program which provides whole grains and foods low in sodium, sugar, and fat to people with chronic disease. As a pilot initiative developed during the COVID-19 pandemic, the Specialty Box Program used a mobile food pharmacy and home-delivery services to increase access to healthier foods. The request for specialty boxes more than doubled the program's initial goal, showing a continued need for healthier food options beyond the pilot phase. Through Loaves & Fishes' infrastructure, we leveraged our current partnerships, funding resources, and response plans. The result was a sustainable program that can be replicated in other areas where nutrition security is inadequate.


Subject(s)
COVID-19 , Food Assistance , Humans , United States , Pandemics , Food Insecurity , North Carolina , Chronic Disease , Food Supply
2.
Br J Haematol ; 195(3): 429-432, 2021 11.
Article in English | MEDLINE | ID: mdl-34254289

ABSTRACT

Ruxolitinib for steroid-refractory acute graft-versus-host disease (SR-aGVHD) results in resistance or intolerance in 1/5 of patients. Outcomes of such patients are undefined. We identified these patients in a multicentre review and reported outcomes. Ruxolitinib-resistant aGVHD was identified in 48/307 patients. Among patients receiving additional therapy, the overall response rate to next therapy was 36%. Median survival was 21 days. Ruxolitinib intolerance led to treatment discontinuation in 16/307 patients. Ten intolerant patients received additional therapy with 50% experiencing continued improvement of aGVHD. Median survival was 50 days in these patients. These data serve as a baseline for future SR-aGVHD studies.


Subject(s)
Graft vs Host Disease/drug therapy , Nitriles/pharmacology , Pyrazoles/pharmacology , Pyrimidines/pharmacology , Acute Disease , Adult , Aged , Allografts , Bone Marrow Transplantation/adverse effects , Cord Blood Stem Cell Transplantation/adverse effects , Drug Resistance , Female , Graft vs Host Disease/mortality , Graft vs Host Disease/prevention & control , Humans , Immunosuppressive Agents/therapeutic use , Male , Middle Aged , Nitriles/adverse effects , Nitriles/therapeutic use , Peripheral Blood Stem Cell Transplantation/adverse effects , Pyrazoles/adverse effects , Pyrazoles/therapeutic use , Pyrimidines/adverse effects , Pyrimidines/therapeutic use , Retrospective Studies , Salvage Therapy , Young Adult
3.
J Clin Apher ; 36(4): 553-562, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33710672

ABSTRACT

Administration of plerixafor with granulocyte-colony stimulating factor (G-CSF) mobilizes CD34+ cells much more effectively than G-CSF alone, but cost generally limits plerixafor use to patients at high risk of insufficient CD34+ cell collection based on low peripheral blood (PB) CD34+ counts following 4 days of G-CSF. We analyzed costs associated with administering plerixafor to patients with higher day 4 CD34+ cell counts to decrease apheresis days and explored the use of a fixed split dose of plerixafor instead of weight-based dosing. We analyzed 235 patients with plasma cell disorders or non-Hodgkin's lymphoma who underwent progenitor cell mobilization and autologous hematopoietic cell transplantation (AHCT) between March 2014 and December 2017. Two hundred ten (89%) received G-CSF plus Plerixafor and 25 (11%) received G-CSF alone. Overall, 180 patients (77%) collected in 1 day, 53 (22%) in 2 days and 2 (1%) in 3 days. Based on our data, we present a probabilistic algorithm to identify patients likely to require more than one day of collection using G-CSF alone. CD34+ cell yield, ANC and platelet recovery were not significantly different between fixed and standard dose plerixafor. Plerixafor enabled collection in 1 day and with estimated savings of $5000, compared to patients who did not receive plerixafor and required collection for three days. While collection and processing costs and patient populations vary among institutions, our results suggest re-evaluation of current algorithms.


Subject(s)
Hematopoietic Stem Cell Mobilization/economics , Hematopoietic Stem Cell Transplantation/economics , Hematopoietic Stem Cell Transplantation/methods , Stem Cells/chemistry , Adult , Aged , Algorithms , Cost Savings , Female , Filgrastim/pharmacology , Granulocyte Colony-Stimulating Factor , Health Care Costs , Humans , Lymphoma, Non-Hodgkin/economics , Lymphoproliferative Disorders/economics , Male , Middle Aged , Prospective Studies , Risk , Stem Cells/cytology , Transplantation, Autologous , Young Adult
4.
Biol Blood Marrow Transplant ; 25(4): 785-790, 2019 04.
Article in English | MEDLINE | ID: mdl-30579967

ABSTRACT

Hemorrhagic cystitis (HC) is a common and important complication of allogeneic hematopoietic cell transplantation (HCT). Reactivation of BK virus is its most common cause. The more intense immunosuppressive regimens administered to recipients of grafts from alternative donors have been reported to account for the increased susceptibility to HC in this population. This study compares patients undergoing HCT with either a haploidentical donor or a matched related donor, all of whom received identical immunosuppression with a post-transplantation cyclophosphamide-based regimen. The incidence of HC was significantly higher in the patients receiving a haploidentical graft (P = .01). The higher incidence of HC in haploidentical graft recipients is therefore directly related to the inherent immune deficiency that follows HLA-mismatched transplantation, independent of the intensity of pharmacologic immunosuppression. This finding carries significant clinical impact for the prevention and treatment of HC in haploidentical graft recipients.


Subject(s)
Cystitis/etiology , Hematopoietic Stem Cell Transplantation/adverse effects , Hemorrhage/etiology , Transplantation Conditioning/adverse effects , Transplantation, Haploidentical/adverse effects , Adolescent , Adult , Aged , Female , Hematopoietic Stem Cell Transplantation/methods , Humans , Incidence , Male , Middle Aged , Transplantation Conditioning/methods , Transplantation, Haploidentical/methods , Young Adult
SELECTION OF CITATIONS
SEARCH DETAIL