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1.
Artigo em Inglês | MEDLINE | ID: mdl-39210724

RESUMO

OBJECTIVE: To evaluate diagnostic trends in pediatric and adult patients presenting for multidisciplinary subspecialty evaluation of dizziness and imbalance across the lifespan. STUDY DESIGN: Retrospective chart review. SETTING: Single pediatric and single adult academic tertiary care hospital. METHODS: Retrospective review of electronic health record for patients presenting to an adult or pediatric multidisciplinary vestibular clinic from 2017 to 2020, including clinical data, physical therapy evaluation, and audiovestibular testing. RESULTS: A total of 1934 patients aged 1 to 95 were evaluated. Most patients were female (n = 1188, 61%); the largest cohort was in the fifth decade of life (n = 321, 17%). Seventy-six percent of patients (n = 1470) were assigned a pathologic diagnosis. Central causes of dizziness were most common in children and young adults, comprising 38% to 54% of all diagnoses in ages 1 to 30. The proportion of peripheral vestibular disorders increased with age, peaking at 32% in ages 61 to 70. Vestibular migraine was the most common pathologic diagnosis in ages 6 to 20 (n = 110, 39%) and 31 and 50 (n = 69, 17%) regardless of gender, but was more prevalent in females (21% vs 14%; P < .0001). The prevalence of benign paroxysmal positional vertigo (BPPV) increased throughout the lifespan, peaking at age 71 to 80. Meniere's disease (MD) did not occur within the first decade of life, but increased thereafter, peaking at ages 51 to 60. CONCLUSION: Multidisciplinary vestibular evaluation resulted in a diagnosis for the majority of patients. Vestibular diagnoses vary across the lifespan however among most age groups, central disorders, including migraine disorders, outnumber peripheral vestibulopathies. The prevalence of peripheral vestibular disorders such as BPPV and MD increased with age. LEVEL OF EVIDENCE: Level IV.

2.
JAMA Dermatol ; 160(7): 741-745, 2024 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-38809569

RESUMO

Importance: Masculinizing gender-affirming hormonal therapy is associated with the development of acne. While isotretinoin is a highly effective acne treatment, little is known about its effectiveness and safety among transgender and gender-diverse individuals receiving gender-affirming hormonal therapy. Objective: To evaluate clinical outcomes of isotretinoin among transgender and gender-diverse individuals receiving gender-affirming hormonal therapy. Design, Setting, and Participants: This multicenter retrospective case series study was conducted at 4 medical centers: Mass General Brigham, University of Pennsylvania, Emory University, and Fenway Health. It included patients aged between 12 and 49 years who were receiving masculinizing gender-affirming hormonal therapy and prescribed isotretinoin for the management of acne between August 14, 2015, and September 20, 2023. Exposure: Isotretinoin therapy for the management of acne. Main Outcomes and Measures: The percentage of patients experiencing improvement or clearance of acne, as well as rates of acne recurrence. Adverse effects and reasons for treatment discontinuation were also evaluated. Results: Among 55 included patients, the mean (SD) age was 25.4 years; 4 (7.3%) were Asian, 2 (3.6%) were Black, 4 (7.2%) were Hispanic, 1 was (1.8%) multiracial, and 36 (65.5%) were White. The median isotretinoin course duration was 6 months (IQR, 4.0-8.0), with a median cumulative dose of 132.7 mg/kg (IQR, 66.4-168.5); the cumulative dose was less than 90 mg/kg for 16 patients (29.1%) and less than 120 mg/kg for 22 patients (40.0%). Isotretinoin was associated with improvement in 48 patients (87.3%) and clearance in 26 patients (47.3%). For the 33 patients treated with a cumulative dose of 120 mg/kg or more, these rates increased to 32 patients (97.0%) and 21 patients (63.6%), respectively. Among the 20 patients who achieved acne clearance and had any subsequent health care encounters, the risk of recurrence was 20.0% (n = 4). The most frequently reported adverse effects were dryness (n = 44; 80.0%), joint pain (n = 8; 14.5%), and eczema (n = 5; 9.1%). Laboratory abnormalities were uncommon. Reasons for premature treatment discontinuation included cost, pharmacy issues, adverse effects, logistical reasons (scheduling), and wound healing concerns for gender-affirming surgery. Conclusion and Relevance: In this case series study of individuals with acne who were receiving masculinizing gender-affirming hormonal therapy and underwent isotretinoin treatment, isotretinoin was often effective and well tolerated. However, premature treatment discontinuation was common and associated with poorer outcomes. Further efforts are needed to understand optimal dosing and treatment barriers to improve outcomes in transgender and gender-diverse individuals receiving masculinizing gender-affirming hormonal therapy.


Assuntos
Acne Vulgar , Fármacos Dermatológicos , Isotretinoína , Pessoas Transgênero , Humanos , Isotretinoína/administração & dosagem , Isotretinoína/efeitos adversos , Acne Vulgar/tratamento farmacológico , Estudos Retrospectivos , Masculino , Feminino , Pessoas Transgênero/estatística & dados numéricos , Adolescente , Adulto , Fármacos Dermatológicos/administração & dosagem , Fármacos Dermatológicos/efeitos adversos , Adulto Jovem , Criança , Resultado do Tratamento , Pessoa de Meia-Idade , Recidiva
3.
Curr Oncol ; 31(2): 918-932, 2024 02 06.
Artigo em Inglês | MEDLINE | ID: mdl-38392062

RESUMO

Financial toxicity adversely affects quality of life and treatment outcomes for patients with cancer. This scoping review examined interventions aimed at mitigating financial toxicity in adult patients with cancer and their effectiveness. We utilized five bibliographical databases to identify studies that met our inclusion criteria. The review included studies conducted among adult patients with cancer in the United States and published in English between January 2011 to March 2023. The review identified eight studies that met the inclusion criteria. Each of the studies discussed the implementation of interventions at the patient/provider and/or health system level. Collectively, the findings from this scoping review highlight both the limited number of published studies that are aimed at mitigating financial toxicity and the need to create and assess interventions that directly impact financial toxicity in demographically diverse populations of adult patients with cancer.


Assuntos
Neoplasias , Qualidade de Vida , Adulto , Humanos , Estados Unidos , Estresse Financeiro , Resultado do Tratamento , Neoplasias/tratamento farmacológico
6.
Naunyn Schmiedebergs Arch Pharmacol ; 389(1): 117-30, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26497184

RESUMO

Ferulic acid ethyl ester (FAEE) is a derivate from ferulic acid which reportedly has antioxidant effect; however, its role on inflammation was unknown. In this study, we investigated the orally administered FAEE anti-inflammatory activity on experimental inflammation models and Complete Freund's Adjuvant (CFA)-induced arthritis in rats. CFA-induced arthritis has been evaluated by incapacitation model and radiographic knee joint records at different observation time. FAEE (po) reduced carrageenan-induced paw edema (p < 0.001) within the 1st to 5th hours at 50 and 100 mg/kg doses. FAEE 50 and 100 mg/kg, po inhibited leukocyte migration into air pouch model (p < 0.001), and myeloperoxidase, superoxide dismutase, and catalase activities (p < 0.001) increased total thiol concentration and decreased the TNF-α and IL-1ß concentrations, NO, and thiobarbituric acid reactive species. In the CFA-induced arthritis, FAEE 50 and 100 mg/kg significantly reduced the edema and the elevation paw time, a joint disability parameter, since second hour after arthritis induction (p < 0.001). FAEE presented rat joint protective activity in radiographic records (p < 0.001). The data suggest that the FAEE exerts anti-inflammatory activity by inhibiting leukocyte migration, oxidative stress reduction, and pro-inflammatory cytokines.


Assuntos
Anti-Inflamatórios/uso terapêutico , Antioxidantes/uso terapêutico , Artrite Experimental/tratamento farmacológico , Ácidos Cafeicos/uso terapêutico , Edema/tratamento farmacológico , Animais , Anti-Inflamatórios/farmacologia , Antioxidantes/farmacologia , Artrite Experimental/diagnóstico por imagem , Artrite Experimental/metabolismo , Artrite Experimental/patologia , Ácidos Cafeicos/farmacologia , Carragenina , Catalase/metabolismo , Movimento Celular/efeitos dos fármacos , Edema/induzido quimicamente , Feminino , Adjuvante de Freund , Glutationa/metabolismo , Interleucina-1beta/metabolismo , Articulação do Joelho/diagnóstico por imagem , Articulação do Joelho/efeitos dos fármacos , Articulação do Joelho/patologia , Leucócitos/efeitos dos fármacos , Leucócitos/fisiologia , Masculino , Camundongos , Atividade Motora/efeitos dos fármacos , Nitritos/metabolismo , Radiografia , Ratos Wistar , Superóxido Dismutase/metabolismo , Substâncias Reativas com Ácido Tiobarbitúrico/metabolismo , Fator de Necrose Tumoral alfa/metabolismo
7.
Rev. bras. ortop ; 46(supl.4): 10-13, 2011. ilus, graf, tab
Artigo em Português | LILACS | ID: lil-611432

RESUMO

Objetivo: Aplicação e correlação do índice de alteração da marcha (GDI) com questionário de avaliação funcional (FAQ), escala de mobilidade funcional (FMS) e índice de Sutherland (IS) para pacientes com distrofia muscular de Duchenne (DMD). Métodos: Onze crianças com diagnóstico clínico de DMD, idade entre 6-11 anos, deambuladoras, participaram do estudo. O GDI foi correlacionado com o FAQ, FMS e IS, utilizando o coeficiente de correlação rho de Spearman-Rank. O GDI foi calculado com a cinemática dos membros inferiores coletada com seis câmeras Hawks da Motion Analysis Corporation. Resultados: O GDI médio obtido foi de 82,5 (± 13,5), sendo este valor menor do que o esperado para indivíduos sem patologias musculoesqueléticas (i.e. ≥ 100). O GDI apresentou correlação moderada com o FAQ e FMS (50/500m) e forte com IS (rho > 0,83, p ≤ 0,05). Conclusão: O GDI apresenta correlação com classificações, sejam elas clínicas (i.e. FMS), por estudo do movimento (i.e. IS) e com questionário de avaliação funcional (i.e. FAQ).


Objective: Aplication and correlation at Gait Deviation Index (GDI) and Functional Assessment Questionnaire (FAQ), Functional Mobility Scale (FMS) and Sutherland Index (SI) for patients with DMD. Methods: Eleven children with clinical diagnosis at Duchenne Muscular Dystrophy (DMD), between 6 and 11 years old, walkers, participated at study. The GDI was correlated with the FAQ, FMS and IS, using the rho coefficient of correlation of Spearman-Rank. To calculate the GDI, the kinematics were collected by six Hawks cameras (Motion Analysis Corporation). Results: The average GDI achieved was 82.5 (plus or minus 13.5), this value being lower than expected for individuals without musculoskeletal disorders (ie greater than or equal to 100). GDI showed moderate correlation with the FMS and FAQ (50/500m) and strong with IS (rho>0.83, p<= 0.05). Conclusion: The GDI shows correlation with clinical classifications (FMS), gait analysis classifications (IS) and questionnaries of function evaluation (FAQ).


Assuntos
Humanos , Masculino , Criança , Marcha , Distrofia Muscular de Duchenne , Inquéritos e Questionários
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