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1.
J Aging Phys Act ; 30(1): 65-72, 2022 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-34384049

RESUMO

Walking interventions improve health outcomes among older adults. However, few clinical trials evaluate long-term behavior change adherence. The authors explored factors that influence walking adherence in older adults following their participation in a clinical trial. They conducted n = 7 focus groups with n = 23 participants enrolled in the parent study (ClinicalTrials.gov number: NCT03654807). The authors used content analysis to code data according to the social-ecological model. They found that supportive services (exercise classes) in retirement communities have multilevel impacts on adherence to walking activity. Residents from communities offering services continued walking because of increased confidence gained in the parent trial, while residents in communities without services were motivated by their functional improvements. Residents voiced frustration with retirement community physical activity programs that did not address the full spectrum of physical functioning. Findings support the need for retirement communities to account for various motivational factors in tailoring programs to promote increased physical activity for older adults.


Assuntos
Aposentadoria , Caminhada , Idoso , Exercício Físico , Grupos Focais , Humanos , Motivação
2.
Pediatr Blood Cancer ; 68(8): e28936, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-33580918

RESUMO

OBJECTIVES: Clinical studies have shown low toxicity and a favorable safety profile for sirolimus in vascular anomalies. Here, we describe severe adverse events (SAEs) observed during "off-label use" for vascular anomalies. METHODS: We performed a retrospective, multicenter chart review for SAEs during "off-label" sirolimus therapy for vascular anomalies and analyzed these cases by a predesigned workflow. RESULTS: We identified 17 SAEs in 14 patients diagnosed with generalized lymphatic anomaly (n = 4), Gorham-Stout disease (n = 2), central conducting lymphatic anomaly (n = 1), lymphatic malformation (n = 4), tufted angioma (n = 1), kaposiform hemangioendothelioma (n = 1), and venous malformation in a patient with CLOVES syndrome (n = 1). Three patients presented two SAEs each. The age at initiation of sirolimus therapy was under 2 years (n = 5), 2-6 years (n = 5), and older than 12 years (n = 4). SAEs occurred during the first 3 months of sirolimus therapy (n = 7), between 3 and 12 months (n = 7) and after 1 year of therapy (n = 3). The most frequent SAE was viral pneumonia (n = 8) resulting in one death due to a metapneumovirus infection in a 3 months old and a generalized adenovirus infection in a 28-month-old child. Sirolimus blood level at the time of SAEs ranged between 2.7 and 21 ng/L. Five patients were on antibiotic prophylaxis. CONCLUSIONS: Most SAEs are observed in the first year of sirolimus therapy; however, SAEs can also occur after a longer treatment period. SAEs are potentially life threatening, especially in early infancy. Presence of other risk factors, that is, underlying vascular anomaly or immune status, may contribute to the risk of SAEs. Sirolimus is an important therapeutic option for vascular anomalies, but patients and physicians need to be aware that adequate monitoring is necessary, especially in patients with complex lymphatic anomalies that are overrepresented in our cohort of SAEs.


Assuntos
Malformações Vasculares , Pré-Escolar , Hemangioendotelioma , Humanos , Lactente , Síndrome de Kasabach-Merritt/tratamento farmacológico , Anormalidades Linfáticas/tratamento farmacológico , Uso Off-Label , Estudos Retrospectivos , Sirolimo/efeitos adversos , Malformações Vasculares/tratamento farmacológico
3.
Biomedica ; 37(3): 303-307, 2017 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-28968006

RESUMO

We report the case of a 61 year-old male who underwent heart transplantation eight months before developing a systemic condition with central nervous system, lung, kidney, colonic, cutaneous, and hematologic involvement, found to be secondary to a systemic toxoplasmosis despite co-trimoxazole prophylaxis in a previous-to-transplant seronegative patient receiving a heart from a seropositive donor. A review of prophylactic options in our environment is discussed.


Assuntos
Transplante de Coração , Complicações Pós-Operatórias/etiologia , Toxoplasmose/transmissão , Anticorpos Antiprotozoários/sangue , Antivirais/uso terapêutico , Terapia Combinada , Infecções por Citomegalovirus/tratamento farmacológico , Infecções por Citomegalovirus/transmissão , Progressão da Doença , Humanos , Imunoglobulinas Intravenosas/uso terapêutico , Imunossupressores/efeitos adversos , Masculino , Pessoa de Meia-Idade , Troca Plasmática , Complicações Pós-Operatórias/parasitologia , Complicações Pós-Operatórias/prevenção & controle , Recidiva , Soroconversão , Doadores de Tecidos , Toxoplasmose/prevenção & controle , Combinação Trimetoprima e Sulfametoxazol/administração & dosagem , Viremia/tratamento farmacológico , Viremia/transmissão
4.
Biomédica (Bogotá) ; 37(3): 303-307, jul.-set. 2017. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-888470

RESUMO

Resumen Se reporta el caso de un paciente de sexo masculino, de 61 años de edad, quien ocho meses después de someterse a un trasplante de corazón presentó una enfermedad sistémica con compromiso del sistema nervioso central y del sistema inmunológico, así como de pulmón, riñón, colon y piel, y a quien finalmente se le diagnosticó toxoplasmosis diseminada, a pesar de haber recibido profilaxis con trimetoprim-sulfametoxazol, debido a que el órgano provenía de un donante positivo para toxoplasmosis siendo él un receptor negativo. Se discuten las opciones de profilaxis en nuestro medio.


Abstract We report the case of a 61 year-old male who underwent heart transplantation eight months before developing a systemic condition with central nervous system, lung, kidney, colonic, cutaneous, and hematologic involvement, found to be secondary to a systemic toxoplasmosis despite co-trimoxazole prophylaxis in a previous-to-transplant seronegative patient receiving a heart from a seropositive donor. A review of prophylactic options in our environment is discussed.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Complicações Pós-Operatórias/etiologia , Toxoplasmose/transmissão , Transplante de Coração , Antivirais/uso terapêutico , Troca Plasmática , Complicações Pós-Operatórias/parasitologia , Complicações Pós-Operatórias/prevenção & controle , Recidiva , Doadores de Tecidos , Viremia/tratamento farmacológico , Viremia/transmissão , Anticorpos Antiprotozoários/sangue , Combinação Trimetoprima e Sulfametoxazol/administração & dosagem , Toxoplasmose/prevenção & controle , Imunoglobulinas Intravenosas/uso terapêutico , Terapia Combinada , Infecções por Citomegalovirus/tratamento farmacológico , Infecções por Citomegalovirus/transmissão , Progressão da Doença , Soroconversão , Imunossupressores/efeitos adversos
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