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1.
Can J Cardiol ; 34(12): 1553-1563, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30527143

RESUMO

Familial hypercholesterolemia (FH) is the most common monogenic disorder causing premature atherosclerotic cardiovascular disease. It affects 1 in 250 individuals worldwide, and of the approximately 145,000 Canadians estimated to have FH, most are undiagnosed. Herein, we provide an update of the 2014 Canadian Cardiovascular Society position statement on FH addressing the need for case identification, prompt recognition, and treatment with statins and ezetimibe, and cascade family screening. We provide a new Canadian definition for FH and tools for clinicians to make a diagnosis. The risk of atherosclerotic cardiovascular disease in patients with "definite" FH is 10- to 20-fold that of a normolipidemic individual and initiating treatment in youth or young adulthood can normalize life expectancy. Target levels for low-density lipoprotein cholesterol are proposed and are aligned with the Canadian Cardiovascular Society guidelines on dyslipidemia. Recommendation for the use of inhibitors of proprotein convertase kexin/subtilisin type 9 are made in patients who cannot achieve therapeutic low-density lipoprotein cholesterol targets on maximally tolerated statins and ezetimibe. The writing committee used the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) methodology in the preparation of the present document, which offers guidance for practical evaluation and management of patients with FH. This position statement also aims to raise awareness of FH nationally, and to mobilize patient support, promote knowledge translation, and availability of treatment and health care resources for this under-recognized, but important medical condition.


Assuntos
Hiperlipoproteinemia Tipo II , Programas de Rastreamento , Anticolesterolemiantes/uso terapêutico , Valva Aórtica/diagnóstico por imagem , Remoção de Componentes Sanguíneos , Canadá , Artérias Carótidas/diagnóstico por imagem , Contraindicações de Medicamentos , Doença da Artéria Coronariana/etiologia , Doença da Artéria Coronariana/prevenção & controle , Diabetes Mellitus Tipo 2/complicações , Feminino , Testes Genéticos , Comportamentos Relacionados com a Saúde , Humanos , Inibidores de Hidroximetilglutaril-CoA Redutases/uso terapêutico , Hiperlipoproteinemia Tipo II/diagnóstico , Hiperlipoproteinemia Tipo II/genética , Hiperlipoproteinemia Tipo II/terapia , Estilo de Vida , Lipídeos/sangue , Gravidez , Prevenção Primária , Sistema de Registros , Medição de Risco , Calcificação Vascular/diagnóstico por imagem
2.
CMAJ ; 190(17): E545, 2018 04 30.
Artigo em Inglês | MEDLINE | ID: mdl-29712675
3.
Head Neck ; 39(6): 1234-1238, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-27862538

RESUMO

BACKGROUND: The incidence of radiation-induced hypothyroidism (RIH) in patients with head and neck cancer is >50%. The purpose of this study was to assess the long-term efficacy of free thyroid transfer (FTT) for prevention of RIH in patients with head and neck cancer. METHODS: Hemithyroid dissection was completed in 10 patients with advanced head and neck cancer undergoing ablation, radial forearm free flap (RFFF) reconstruction, and postoperative radiotherapy (RT). The hemithyroid was anastomosed to the donor site vessels in the forearm. Thyroid laboratory testing and technetium (Tc) scans were performed 6 weeks and 12 months postoperatively to establish functional integrity. RESULTS: FTT was successfully performed in 9 of 10 recruited patients. Postoperative Tc scans demonstrated strong Tc uptake in the forearm donor site at 6 weeks and 12 months in all patients who underwent transplantations. CONCLUSION: FTT is feasible with maintenance of function, and may represent a novel strategy for prevention of RIH. © 2016 Elsevier Head & Neck Published by Wiley Periodicals, Inc. Head Neck 39: 1234-1238, 2017.


Assuntos
Retalhos de Tecido Biológico/transplante , Neoplasias de Cabeça e Pescoço/radioterapia , Hipotireoidismo/prevenção & controle , Procedimentos de Cirurgia Plástica/métodos , Glândula Tireoide/cirurgia , Tireoidectomia/métodos , Idoso , Estudos de Viabilidade , Feminino , Seguimentos , Retalhos de Tecido Biológico/irrigação sanguínea , Sobrevivência de Enxerto , Neoplasias de Cabeça e Pescoço/patologia , Neoplasias de Cabeça e Pescoço/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Invasividade Neoplásica/patologia , Estadiamento de Neoplasias , Estudos Prospectivos , Dosagem Radioterapêutica , Radioterapia Adjuvante/efeitos adversos , Glândula Tireoide/transplante , Tireoidectomia/efeitos adversos , Resultado do Tratamento
4.
Int J Radiat Oncol Biol Phys ; 96(1): 42-5, 2016 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-27511845

RESUMO

PURPOSE: The incidence of hypothyroidism after radiation therapy for head and neck cancer (HNC) has been found to be ≤53%. Medical treatment of hypothyroidism can be costly and difficult to titrate. The aim of the present study was to assess the feasibility of free thyroid transfer as a strategy for the prevention of radiation-induced damage to the thyroid gland during radiation therapy for HNC. METHODS AND MATERIALS: A prospective feasibility study was performed involving 10 patients with a new diagnosis of advanced HNC undergoing ablative surgery, radial forearm free-tissue transfer reconstruction, and postoperative adjuvant radiation therapy. During the neck dissection, hemithyroid dissection was completed with preservation of the thyroid arterial and venous supply for implantation into the donor forearm site. All patients underwent a diagnostic thyroid technetium scan 6 weeks and 12 months postoperatively to examine the functional integrity of the transferred thyroid tissue. RESULTS: Free thyroid transfer was executed in 9 of the 10 recruited patients with advanced HNC. The postoperative technetium scans demonstrated strong uptake of technetium at the forearm donor site at 6 weeks and 12 months for all 9 of the transplanted patients. CONCLUSIONS: The thyroid gland can be transferred as a microvascular free transfer with maintenance of function. This technique could represent a novel strategy for maintenance of thyroid function after head and neck irradiation.


Assuntos
Neoplasias de Cabeça e Pescoço/radioterapia , Hipotireoidismo/etiologia , Hipotireoidismo/cirurgia , Lesões por Radiação/etiologia , Lesões por Radiação/cirurgia , Glândula Tireoide/transplante , Feminino , Retalhos de Tecido Biológico , Neoplasias de Cabeça e Pescoço/complicações , Neoplasias de Cabeça e Pescoço/cirurgia , Humanos , Hipotireoidismo/diagnóstico , Masculino , Pessoa de Meia-Idade , Lesões por Radiação/diagnóstico , Resultado do Tratamento
5.
Clin Interv Aging ; 11: 73-81, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26869776

RESUMO

BACKGROUND: Elderly people (aged 65 years or more) are at increased risk of polypharmacy (five or more medications), inappropriate medication use, and associated increased health care costs. The use of clinical decision support (CDS) within an electronic medical record (EMR) could improve medication safety. METHODS: Participatory action research methods were applied to preproduction design and development and postproduction optimization of an EMR-embedded CDS implementation of the Beers' Criteria for medication management and the Cockcroft-Gault formula for estimating glomerular filtration rates (GFR). The "Seniors Medication Alert and Review Technologies" (SMART) intervention was used in primary care and geriatrics specialty clinics. Passive (chart messages) and active (order-entry alerts) prompts exposed potentially inappropriate medications, decreased GFR, and the possible need for medication adjustments. Physician reactions were assessed using surveys, EMR simulations, focus groups, and semi-structured interviews. EMR audit data were used to identify eligible patient encounters, the frequency of CDS events, how alerts were managed, and when evidence links were followed. RESULTS: Analysis of subjective data revealed that most clinicians agreed that CDS appeared at appropriate times during patient care. Although managing alerts incurred a modest time burden, most also agreed that workflow was not disrupted. Prevalent concerns related to clinician accountability and potential liability. Approximately 36% of eligible encounters triggered at least one SMART alert, with GFR alert, and most frequent medication warnings were with hypnotics and anticholinergics. Approximately 25% of alerts were overridden and ~15% elicited an evidence check. CONCLUSION: While most SMART alerts validated clinician choices, they were received as valuable reminders for evidence-informed care and education. Data from this study may aid other attempts to implement Beers' Criteria in ambulatory care EMRs.


Assuntos
Sistemas de Apoio a Decisões Clínicas/estatística & dados numéricos , Conduta do Tratamento Medicamentoso/normas , Lista de Medicamentos Potencialmente Inapropriados , Atenção Primária à Saúde/normas , Idoso , Interações Medicamentosas , Feminino , Humanos , Entrevistas como Assunto , Masculino , Médicos , Polimedicação
7.
Can J Cardiol ; 22(11): 939-45, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16971979

RESUMO

INTRODUCTION: Ezetimibe (EZ) is a selective cholesterol absorption inhibitor approved for use in Canada. The effect and tolerability of EZ among patients was evaluated in the clinical setting of a specialty cardiovascular risk reduction clinic at the University of Alberta Hospital, Edmonton, Alberta. patients and METHODS: All patients 18 years of age or older who were prescribed EZ were included, unless they failed to take EZ for a minimum of two weeks, did not have baseline and on-EZ low-density lipoprotein cholesterol (LDL-C) levels, or had concomitant lipid-lowering drugs or dosages changed within one month of starting EZ. RESULTS: Eighty-four patients (mean age 57.9 years) were included. By Framingham risk calculation, 71.4% were found to be high-risk patients, 13.1% moderate-risk patients and 15.5% low-risk patients; 66.7% of patients had prior cardiovascular events. On EZ, the mean reductions were: total cholesterol level 1.11 mmol/L (16.5%); LDL-C level 1.01 mmol/L (22.3%); high-density lipoprotein cholesterol level 0.06 mmol/L (4.6%); and ratio of total cholesterol level to high-density lipoprotein cholesterol level 0.68 mmol/L (12.8%); all were statistically significant (P<0.001). Results were similar when stratified by primary (n=28) versus secondary (n=56) prevention. Patients on EZ monotherapy (n=34) had mean LDL-C reductions of 1.03 mmol/L (20.5%) compared with 1.19 mmol/L (30.1%) or 0.95 mmol/L (22.5%), where EZ was added to low-dose or high-dose statins (P<0.01 for all). On EZ, 30 patients (35.7%) achieved previously unattainable target LDL-C levels. Four patients discontinued the drug due to side effects. CONCLUSIONS: EZ is safe and effective in high-risk patients treated in the clinical setting of a cardiovascular risk reduction clinic. A mean LDL-C reduction of 1 mmol/L (20% to 30%) in all patient subgroups is consistent with previous clinical trial results. The significant reduction in LDL-C (mean 22.5%) observed in the EZ plus high-dose statin subgroup provides clinical evidence for use of this medication beyond published studies.


Assuntos
Anticolesterolemiantes/uso terapêutico , Azetidinas/uso terapêutico , Doenças Cardiovasculares/epidemiologia , Doenças Cardiovasculares/prevenção & controle , Hiperlipidemias/epidemiologia , Hiperlipidemias/prevenção & controle , Adulto , Idoso , Idoso de 80 Anos ou mais , Alberta/epidemiologia , Instituições de Assistência Ambulatorial , Anticolesterolemiantes/administração & dosagem , Anticolesterolemiantes/efeitos adversos , Azetidinas/administração & dosagem , Azetidinas/efeitos adversos , Doenças Cardiovasculares/sangue , Doenças Cardiovasculares/complicações , Colesterol/sangue , HDL-Colesterol/sangue , LDL-Colesterol/sangue , Estudos de Coortes , Ezetimiba , Feminino , Humanos , Hiperlipidemias/sangue , Hiperlipidemias/complicações , Masculino , Prontuários Médicos , Pessoa de Meia-Idade , Satisfação do Paciente , Estudos Retrospectivos , Triglicerídeos/sangue
8.
Diabetes Care ; 28(4): 810-5, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15793178

RESUMO

OBJECTIVE: To examine whether hyperglycemia at the time of presentation was associated with outcomes in patients admitted to non-intensive care settings with community-acquired pneumonia (CAP). RESEARCH DESIGN AND METHODS: Prospective cohort study of consecutive patients admitted to six hospitals between 15 November 2000 and 14 November 2002. RESULTS: Of the 2,471 patients in this study (median age 75 years), 279 (11%) had serum glucose at presentation >11 mmol/l: 178 of the 401 patients (44%) with a prior diagnosis of diabetes and 101 of the 2,070 patients (5%) without a history of diabetes. Of patients hospitalized with CAP, 9% died and 23% suffered an in-hospital complication. Compared with those with values < or =11 mmol/l, patients with an admission glucose >11 mmol/l had an increased risk of death (13 vs. 9%, P = 0.03) and in-hospital complications (29 vs. 22%, P = 0.01). Compared with those patients with admission glucose < or =6.1 mmol/l, the mortality risk was 73% higher (95% CI 12-168%) and the in-hospital complication risk was 52% higher (12-108%) in patients with admission glucose >11 mmol/l. Even after adjustment for factors in the Pneumonia Severity Index, hyperglycemia on admission remained significantly associated with subsequent adverse outcomes: for each 1-mmol/l increase, risk of in-hospital complications increased 3% (0.2-6%). CONCLUSIONS: Hyperglycemia on admission is independently associated with adverse outcomes in patients with CAP, with the increased risks evident at lower glucose levels than previously reported.


Assuntos
Infecções Comunitárias Adquiridas/complicações , Hiperglicemia/complicações , Pacientes Internados , Pneumonia/complicações , Idoso , Alberta/epidemiologia , Infecções Comunitárias Adquiridas/mortalidade , Feminino , Instituição de Longa Permanência para Idosos , Mortalidade Hospitalar , Humanos , Hiperglicemia/mortalidade , Tempo de Internação , Masculino , Casas de Saúde , Fatores de Risco , Análise de Sobrevida , Resultado do Tratamento
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