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1.
Pediatr Phys Ther ; 33(2): 74-81, 2021 04 01.
Artigo em Inglês | MEDLINE | ID: mdl-33653984

RESUMO

BACKGROUND: Physical therapists (PTs) have a broad range of approaches to the management of Down syndrome (DS). PURPOSE: To examine the breadth of physical therapy practice for children with DS. METHODS: A survey was distributed to 1000 randomly selected members of the Academy of Pediatric Physical Therapy. DATA ANALYSIS: Responses were categorized into 13 thematic subcategories and 3 International Classification of Functioning, Disability and Health (ICF) subcategories. RESULTS AND DISCUSSION: One hundred eight PTs participated. Joint stability and alignment were the most common physical therapy-related problem. Functional movement was the most common physical therapy intervention. Most clinicians identified and treated at the ICF level of body functions and structure. Multiple assessment tools were used and tended to include norm-referenced tests. There was diversity of interventions with varying amounts of supporting evidence. CONCLUSIONS: PTs manage children with DS for a wide variety of needs with a variety of interventions.


Assuntos
Síndrome de Down , Fisioterapeutas , Criança , Avaliação da Deficiência , Humanos , Modalidades de Fisioterapia , Inquéritos e Questionários
2.
Obes Res Clin Pract ; 13(2): 176-179, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30826256

RESUMO

INTRODUCTION: With the epidemic of obesity numerous mobile health (mHealth) applications have been designed with the goal of facilitating weight loss. This technology has the potential to focus behavioral modification in a manner that's effective for weight loss. We examined the use of this mHealth technology in our bariatric surgery population to evaluate effects on weight loss following surgery. METHODS: Single institution prospective randomized control trial performed at an academic center. 56 patients who recently underwent a laparoscopic sleeve gastrectomy (LSG) were enrolled into a control group with standard post-operative monitoring and a mHealth application group provided with iPad© minis with the MyFitnessPal© mHealth application. Participants were followed for 24 months. The primary outcomes were effect on weight loss as determined by excess body weight loss (%EWL) and excess BMI loss (%EBL). RESULTS: Statistically significant differences in weight loss outcomes between the groups were present throughout the duration of the study. At 12 months, %EWL was 74.41% (control) vs 81.41% (mHealth) p value 0.047 and at 24 months, it was 59.10% (control) vs 71.47% (mHealth) p value 0.0078. %EBL findings at 12 months was 28.02% (control) vs 32.15% (mHealth) p value 0.0007 and at 24 months, it was 25.39% (control) vs 27.87% (mHealth) p value 0.048. CONCLUSION: Our results demonstrate mHealth applications are a useful adjunct to improve and maintain weight loss following bariatric surgery. We suggest mHealth applications should be utilized following bariatric surgery for improved outcomes.


Assuntos
Cirurgia Bariátrica , Aplicativos Móveis , Obesidade Mórbida/cirurgia , Cuidados Pós-Operatórios/instrumentação , Telemedicina , Redução de Peso/fisiologia , Programas de Redução de Peso , Adulto , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Obesidade Mórbida/prevenção & controle , Cuidados Pós-Operatórios/métodos , Estudos Prospectivos , Resultado do Tratamento
3.
Curr Probl Diagn Radiol ; 48(2): 111-113, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30121160

RESUMO

With the use of intravenous contrast in medical imaging, radiologists and radiology personnel will inevitably encounter adverse events at their imaging facilities. At our institution, the stress of these emergency scenarios led to disorderly and unsafe responses by the staff. We present a quality improvement project, where our team addressed these unsafe emergency responses. Through explicit role delineation and standardization, we created an effective and efficient emergency response protocol that was replicable throughout our healthcare organization.


Assuntos
Meios de Contraste/efeitos adversos , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/terapia , Emergências , Equipe de Assistência ao Paciente/organização & administração , Papel Profissional , Melhoria de Qualidade , Serviço Hospitalar de Radiologia/organização & administração , Algoritmos , Humanos , Capacitação em Serviço
4.
Int J Risk Saf Med ; 28(2): 101-14, 2016 Aug 22.
Artigo em Inglês | MEDLINE | ID: mdl-27567767

RESUMO

BACKGROUND: Actual assessment methods for identifying adverse events (AEs) in clinical trials have received less scrutiny than underreporting of AEs. OBJECTIVE: To investigate whether AE assessment has changed over time for three psychotropic drugs with turbulent histories of safety concerns since their U.S. approval. METHODS: From industry-funded published trials of atomoxetine, duloxetine, and olanzapine retrieved from PubMed for 1996-2004 (n = 33) and 2009-2014 (n = 40), verbatim AE assessment and numbers of words describing efficacy and safety assessment were extracted. RESULTS: Closest to drug approval (1996-2004), 77.8% of atomoxetine trials used open-ended questioning only, 50% of duloxetine trials used spontaneous self-report or clinician observation only, and 66.7% of olanzapine trials used a scale (primarily for extrapyramidal symptoms) and one former method. Recent studies (2009-2014) showed less rigor and transparency: 35.3% of atomoxetine and 64.7% of duloxetine studies reported no AE assessment method and 50% of olanzapine studies no longer used scales. Overall, the mean number of words describing efficacy assessment increased from 202 to 309 but decreased from 83 to 63 for safety. CONCLUSION: Trial methodology for assessing psychotropic drug safety remains an underdeveloped area with major public health implications.


Assuntos
Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/diagnóstico , Psicotrópicos/efeitos adversos , Sistemas de Notificação de Reações Adversas a Medicamentos/normas , Sistemas de Notificação de Reações Adversas a Medicamentos/estatística & dados numéricos , Ensaios Clínicos como Assunto/métodos , Ensaios Clínicos como Assunto/normas , Revelação , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/etiologia , Humanos , Avaliação das Necessidades , Avaliação de Resultados da Assistência ao Paciente , Melhoria de Qualidade , Projetos de Pesquisa/normas
5.
Pediatr Dermatol ; 32(5): 704-9, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26227567

RESUMO

BACKGROUND: Pediatric toxic epidermal necrolysis (TEN) is a rare and potentially fatal skin disease with a multitude of causative factors and no consensus on treatment guidelines and, as a result, it has a variety of short- and long-term outcomes. We present the experience of a large specialty burn center to share our diagnostic and treatment principles. METHODS: A retrospective review from 1989 to 2010 at the Joseph M. Still Burn Center was performed to find patients with a diagnosis of Steven-Johnson syndrome (SJS) or TEN. Information was obtained on demographic and physiologic parameters such as age, race, total body surface area involved, treatments, hospital stay, and need for ventilator support. RESULTS: We identified SJS or TEN in 21 patients. Prescription drugs were the most common etiology (in 15 patients), with antibiotics as the most common causative agent. Histology confirmed the clinical diagnosis of TEN in 14 patients. Our treatment plan included a multidisciplinary team, early initiation of intravenous immunoglobulin, bronchoscopy, strict management of electrolyte and fluid balances, and meticulous surgical wound care. Mortality was 9.5%. CONCLUSION: Our experience in treating this rare but devastating disease affords us the opportunity to share the diagnostic dilemmas we faced and the treatment principles we used to treat this unique patient population successfully.


Assuntos
Broncoscopia , Unidades de Queimados , Imunoglobulinas Intravenosas/uso terapêutico , Síndrome de Stevens-Johnson/diagnóstico , Síndrome de Stevens-Johnson/tratamento farmacológico , Equilíbrio Hidroeletrolítico , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Tempo de Internação , Masculino , Estudos Retrospectivos , Centros de Atenção Terciária
6.
Ann Vasc Surg ; 29(6): 1307-14, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26004967

RESUMO

BACKGROUND: Vascular injuries are common in trauma and often involve massive soft tissue injury and segmental arterial loss. Current practice uses either autogenous vein or polytetrafluorethylene (PTFE) for interposition grafting in arterial injuries. Decision making between autogenous or synthetic conduit pivots around the physiological state of the trauma patient. Vein is known to increase operative times in an already physiologically depleted patient, whereas synthetic graft can be simply pulled from the shelf. However, when used in contaminated wounds, PTFE is prone to chronic infection and subsequent graft failure. An alternative synthetic conduit resistant to infection would be ideal for such situations. Permacol (Tissue Science Laboratories, Inc, Andover, MA), a biosynthetic material, has demonstrated resistance to bacterial contamination in contaminated hernia repairs. When fashioned into a tubular structure, this material may be useful as an alternative vascular conduit in contaminated trauma wounds. METHODS: New Zealand white rabbits were randomized to one of 4 groups: Permacol graft (P) without bacterial contamination (n = 9), Permacol graft with bacterial contamination (CP; n = 9), autogenous vein graft without bacterial contamination (V; n = 9), or autogenous vein with bacterial contamination (CV; n = 9). All groups then underwent interposition grafting of the right common carotid artery. Grafts were contaminated by applying Staphylococcus aureus (1 × 10(5) colonies/0.1 mL) directly to the exposed surface of the graft on completion of the arterial repair. Each graft was then excised at day 42, and segments were collected for histologic evaluation, bacterial counts, and real-time polymerase chain reaction. RESULTS: Of the 36 rabbits used in this study, 3 animals in the CV group died within 72 hr of surgery. There was no difference in early mortality between P and V (0% vs. 0%; P = 1.0); however, early mortality was higher in the CV compared with the CP group (33% vs. 0%; P = 0.023). At 42 days, histologic evaluation of graft patency demonstrated no difference between P and V (67% vs. 33%; P = 0.157); however, patency was higher in CP than CV (56% vs. 12%; P = 0.040). In addition, no difference was found between the 2 contaminated groups in regard to the number of bacteria present on each graft material. CONCLUSIONS: Permacol as an interposition graft is a feasible alternative to vein in a contaminated setting and shows resistance to infection in a rabbit model. Future studies are needed to evaluate this material in larger animal models.


Assuntos
Implante de Prótese Vascular/instrumentação , Prótese Vascular , Artéria Carótida Primitiva/cirurgia , Colágeno , Veias Jugulares/transplante , Infecções Estafilocócicas/cirurgia , Infecção da Ferida Cirúrgica/cirurgia , Animais , Autoenxertos , Carga Bacteriana , Artéria Carótida Primitiva/microbiologia , Artéria Carótida Primitiva/patologia , Remoção de Dispositivo , Modelos Animais de Doenças , Estudos de Viabilidade , Veias Jugulares/microbiologia , Masculino , Desenho de Prótese , Coelhos , Infecções Estafilocócicas/microbiologia , Infecções Estafilocócicas/patologia , Infecção da Ferida Cirúrgica/microbiologia , Infecção da Ferida Cirúrgica/patologia , Fatores de Tempo
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