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1.
J Hip Preserv Surg ; 10(1): 48-56, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37275836

RESUMO

The 2022 International Society of Hip Preservation (ISHA) physiotherapy agreement on assessment and treatment of greater trochanteric pain syndrome (GTPS) was intended to present a physiotherapy consensus on the assessment and surgical and non-surgical physiotherapy management of patients with GTPS. The panel consisted of 15 physiotherapists and eight orthopaedic surgeons. Currently, there is a lack of high-quality literature supporting non-operative and operative physiotherapy management. Therefore, a group of physiotherapists who specialize in the treatment of non-arthritic hip pathology created this consensus statement regarding physiotherapy management of GTPS. The consensus was conducted using a modified Delphi technique to guide physiotherapy-related decisions according to the current knowledge and expertise regarding the following: (i) evaluation of GTPS, (ii) non-surgical physiotherapy management, (iii) use of corticosteroids and orthobiologics and (iv) surgical indications and post-operative physiotherapy management.

2.
J Hip Preserv Surg ; 7(4): 631-642, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34377507

RESUMO

The 2019 International Society of Hip Preservation (ISHA) physiotherapy agreement on femoroacetabular impingement syndrome (FAIS) was intended to build an international physiotherapy consensus on the assessment, non-surgical physiotherapy treatment, pre-/post-operative management, and return to sport decisions for those patients with FAIS. The panel consisted of 11 physiotherapists and 8 orthopaedic surgeons. There is limited evidence regarding the use of physiotherapy in the overall management of those with FAIS. Therefore, a group of ISHA member physiotherapists, who treat large numbers of FAIS patients and have extensive experience in this area, constructed a consensus statement to guide physiotherapy-related decisions in the overall management of those with FAIS. The consensus was conducted using a modified Delphi technique. Six major topics were the focus of the consensus statement: (i) hip assessment, (ii) non-surgical physiotherapy management, (iii) pre-habilitation prior to hip arthroscopy, (iv) post-operative physiotherapy rehabilitation, (v) stages of post-operative rehabilitation and (vi) return to sports criteria/guidelines after surgery.

4.
J Natl Compr Canc Netw ; 8 Suppl 7: S7-S27, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20947724

RESUMO

REMS are a particularly important issue for oncology and the National Comprehensive Cancer Network (NCCN). A disproportionate number of drugs with complex REMS are used in patients with cancer or hematologic disorders. REMS policies and processes within oncology may act as a model for other clinical areas. A breadth of experience and access to a wide knowledge base exists within oncology that will ensure appropriate development and consideration of the practical implications of REMS. NCCN is uniquely positioned to assume a leadership role in this process given its status as the arbiter of high-quality cancer care based on its world-leading institutions and clinicians. Notwithstanding the potential benefits, the successful design, implementation, and analysis of the FDA's recent requirement for REMS for some high-risk drugs and biologics will present significant challenges for stakeholders, including patients, providers, cancer centers, manufacturers, payors, health information technology vendors, and regulatory agencies. To provide guidance to these stakeholders regarding REMS challenges, the NCCN assembled a work group comprised of thought leaders from NCCN Member Institutions and other outside experts. The Work Group identified challenges across the REMS spectrum, including the areas of standardization, development and assessment of REMS programs, medication guides, provider knowledge and impact on prescribing, provider burden and compensation, and incorporation of REMS into clinical practice.


Assuntos
Comitês Consultivos , Antineoplásicos , Produtos Biológicos , Monitoramento de Medicamentos , Tratamento Farmacológico/normas , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/prevenção & controle , Drogas em Investigação , Oncologia , Medição de Risco , Gestão da Segurança , Comitês Consultivos/organização & administração , Antineoplásicos/uso terapêutico , Produtos Biológicos/uso terapêutico , Indústria Farmacêutica/normas , Indústria Farmacêutica/tendências , Rotulagem de Medicamentos/normas , Rotulagem de Medicamentos/tendências , Monitoramento de Medicamentos/normas , Monitoramento de Medicamentos/tendências , Tratamento Farmacológico/métodos , Tratamento Farmacológico/tendências , Drogas em Investigação/uso terapêutico , Prova Pericial , Pesquisas sobre Atenção à Saúde , Letramento em Saúde , Pessoal de Saúde/economia , Humanos , Comunicação Interdisciplinar , Oncologia/métodos , Oncologia/normas , Oncologia/tendências , Uso Off-Label/normas , Mecanismo de Reembolso , Medição de Risco/métodos , Medição de Risco/normas , Medição de Risco/tendências , Gestão da Segurança/métodos , Gestão da Segurança/normas , Gestão da Segurança/tendências , Estados Unidos , United States Food and Drug Administration/legislação & jurisprudência
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