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1.
Health Promot Pract ; 24(1_suppl): 112S-115S, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-36999496

RESUMEN

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.


Asunto(s)
COVID-19 , Asistencia Alimentaria , Humanos , Estados Unidos , Pandemias , Inseguridad Alimentaria , North Carolina , Enfermedad Crónica , Abastecimiento de Alimentos
2.
Br J Haematol ; 195(3): 429-432, 2021 11.
Artículo en Inglés | MEDLINE | ID: mdl-34254289

RESUMEN

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.


Asunto(s)
Enfermedad Injerto contra Huésped/tratamiento farmacológico , Nitrilos/farmacología , Pirazoles/farmacología , Pirimidinas/farmacología , Enfermedad Aguda , Adulto , Anciano , Aloinjertos , Trasplante de Médula Ósea/efectos adversos , Trasplante de Células Madre de Sangre del Cordón Umbilical/efectos adversos , Resistencia a Medicamentos , Femenino , Enfermedad Injerto contra Huésped/mortalidad , Enfermedad Injerto contra Huésped/prevención & control , Humanos , Inmunosupresores/uso terapéutico , Masculino , Persona de Mediana Edad , Nitrilos/efectos adversos , Nitrilos/uso terapéutico , Trasplante de Células Madre de Sangre Periférica/efectos adversos , Pirazoles/efectos adversos , Pirazoles/uso terapéutico , Pirimidinas/efectos adversos , Pirimidinas/uso terapéutico , Estudios Retrospectivos , Terapia Recuperativa , Adulto Joven
3.
J Clin Apher ; 36(4): 553-562, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-33710672

RESUMEN

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.


Asunto(s)
Movilización de Célula Madre Hematopoyética/economía , Trasplante de Células Madre Hematopoyéticas/economía , Trasplante de Células Madre Hematopoyéticas/métodos , Células Madre/química , Adulto , Anciano , Algoritmos , Ahorro de Costo , Femenino , Filgrastim/farmacología , Factor Estimulante de Colonias de Granulocitos , Costos de la Atención en Salud , Humanos , Linfoma no Hodgkin/economía , Trastornos Linfoproliferativos/economía , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Riesgo , Células Madre/citología , Trasplante Autólogo , Adulto Joven
4.
Biol Blood Marrow Transplant ; 25(4): 785-790, 2019 04.
Artículo en Inglés | MEDLINE | ID: mdl-30579967

RESUMEN

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.


Asunto(s)
Cistitis/etiología , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Hemorragia/etiología , Acondicionamiento Pretrasplante/efectos adversos , Trasplante Haploidéntico/efectos adversos , Adolescente , Adulto , Anciano , Femenino , Trasplante de Células Madre Hematopoyéticas/métodos , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Acondicionamiento Pretrasplante/métodos , Trasplante Haploidéntico/métodos , Adulto Joven
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