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1.
Occup Med (Lond) ; 74(1): 113-119, 2024 02 19.
Artigo em Inglês | MEDLINE | ID: mdl-38330159

RESUMO

BACKGROUND: Prior studies showed that during the coronavirus disease 2019 (COVID-19) pandemic healthcare workers had a higher risk of developing post-traumatic stress disorder (PTSD) symptoms. However, studies conducted among doctors several years after the beginning of the COVID-19 pandemic are scarce. AIMS: To evaluate the prevalence of PTSD among hospital doctors and to describe potential explanatory factors. METHODS: The Protec-Cov study was an observational, cross-sectional, multicentre study, which used an anonymous online questionnaire to evaluate PTSD in doctors from six hospitals in France between December 2021 and March 2022. The presence of PTSD was assessed using the Post-traumatic Stress Disorder Checklist Scale (PCLS) questionnaire with a cut-off of 44. RESULTS: Among the 307 doctors included, 18% presented a PCLS ≥44. The multivariate analysis showed that factors associated with a PCLS ≥44 were having a higher workload than before the COVID-19 pandemic (odds ratio [OR] = 4.75; 95% confidence interval [CI] 1.68-13.38), not feeling recognized within the professional environment (OR = 2.83; 95% CI 1.26-6.33), and feeling isolated because of the lockdown (OR = 4.2; 95% CI 1.97-8.95). Approximately 30% of hospital doctors (n = 91) felt a need for psychological support but only 31% of them (n = 28) received support. CONCLUSIONS: Based on our findings, a high prevalence of PTSD was observed among hospital doctors 2 years after the beginning of the COVID-19 pandemic. This study supports an early diagnosis of PTSD in this category of healthcare workers and warrants further study.


Assuntos
COVID-19 , Transtornos de Estresse Pós-Traumáticos , Humanos , COVID-19/epidemiologia , COVID-19/complicações , Transtornos de Estresse Pós-Traumáticos/epidemiologia , Transtornos de Estresse Pós-Traumáticos/etiologia , Pandemias , Estudos Transversais , Controle de Doenças Transmissíveis , Hospitais
3.
Br J Dermatol ; 185(6): 1232-1239, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34173243

RESUMO

BACKGROUND: European guidelines propose a 0·5 mg kg-1 per day dose of oral prednisone as initial treatment for bullous pemphigoid (BP). We assessed the safety and efficacy of this regimen depending on BP extent and general condition of the patients. METHODS: In a prospective international study, we consecutively included all patients diagnosed with BP. Patients received a 0·5 mg kg-1 per day dose of prednisone, which was then gradually tapered 15 days after disease control, with the aim of stopping prednisone or maintaining minimal treatment (0·1 mg kg-1 per day) within 6 months after the start of treatment. The two coprimary endpoints were control of disease activity at day 21 and 1-year overall survival. Disease severity was assessed according to the Bullous Pemphigoid Disease Area Index (BPDAI) score. RESULTS: In total, 198 patients were included between 2015 and 2017. The final analysis comprised 190 patients with a mean age of 80·9 (SD 9·1) years. Control of disease activity was achieved at day 21 in 119 patients [62·6%, 95% confidence interval (CI) 55·3-69.5]; 18 of 24 patients (75%, 95% CI 53·3-90·2), 75 of 110 patients (68·8%, 95% CI 59·2-77·3) and 26 of 56 patients (46.4%, 95% CI 33·0-60·3) had mild, moderate and severe BP, respectively (P = 0·0218). A total of 30 patients died during the study. The overall Kaplan-Meier 1-year survival was 82·6% (95% CI 76·3-87·4) corresponding to 90·9%, 83·0% and 80·0% rates in patients with mild, moderate and severe BP, respectively (P = 0·5). Thresholds of 49 points for BPDAI score and 70 points for Karnofsky score yielded maximal Youden index values with respect to disease control at day 21 and 1-year survival, respectively. CONCLUSIONS: A 0·5 mg kg-1 per day dose of prednisone is a valuable therapeutic option in patients with mild or moderate BP whose general condition allows them to be autonomous.


Assuntos
Penfigoide Bolhoso , Administração Oral , Corticosteroides/uso terapêutico , Idoso de 80 Anos ou mais , Humanos , Penfigoide Bolhoso/diagnóstico , Prednisona/uso terapêutico , Estudos Prospectivos
4.
ESMO Open ; 6(3): 100134, 2021 06.
Artigo em Inglês | MEDLINE | ID: mdl-33984676

RESUMO

BACKGROUND: The impact of the first coronavirus disease 2019 (COVID-19) wave on cancer patient management was measured within the nationwide network of the Unicancer comprehensive cancer centers in France. PATIENTS AND METHODS: The number of patients diagnosed and treated within 17 of the 18 Unicancer centers was collected in 2020 and compared with that during the same periods between 2016 and 2019. Unicancer centers treat close to 20% of cancer patients in France yearly. The reduction in the number of patients attending the Unicancer centers was analyzed per regions and cancer types. The impact of delayed care on cancer-related deaths was calculated based on different hypotheses. RESULTS: A 6.8% decrease in patients managed within Unicancer in the first 7 months of 2020 versus 2019 was observed. This reduction reached 21% during April and May, and was not compensated in June and July, nor later until November 2020. This reduction was observed only for newly diagnosed patients, while the clinical activity for previously diagnosed patients increased by 4% similar to previous years. The reduction was more pronounced in women, in breast and prostate cancers, and for patients without metastasis. Using an estimated hazard ratio of 1.06 per month of delay in diagnosis and treatment of new patients, we calculated that the delays observed in the 5-month period from March to July 2020 may result in an excess mortality due to cancer of 1000-6000 patients in coming years. CONCLUSIONS: In this study, the delays in cancer patient management were observed only for newly diagnosed patients, more frequently in women, for breast cancer, prostate cancer, and nonmetastatic cancers. These delays may result is an excess risk of cancer-related deaths in the coming years.


Assuntos
COVID-19 , Neoplasias/complicações , COVID-19/complicações , Feminino , França , Humanos , Masculino , SARS-CoV-2
5.
Clin Nutr ; 39(6): 1900-1907, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31471163

RESUMO

BACKGROUND & AIMS: Malnutrition affects 5-10% of elderly people living in the community. A few studies suggest that nutritional intervention may reduce health care costs. The present study included malnourished elderly patients living at home. It aimed to compare health care costs between patients that were prescribed ONS by their general practitioner and those who were not, and to assess the effect of ONS prescription on the risk of hospitalisation. METHODS: This prospective multicentre observational study included malnourished patients ≥70 years old who lived at home. Patients were defined as malnourished if they presented with one or more of the following criteria: weight loss ≥5% in 1 month, weight loss ≥10% in 6 months, BMI <21 kg/m2, albuminemia <35 g/L or Short-Form MNA ≤ 7. Their general practitioners prescribed an ONS, or not, according to their usual practice. Health care costs were recorded during a 6-month period. Other collected data were diseases, disability, self-perception of current health status, quality of life (QoL), nutritional status, appetite and compliance to ONS. A propensity score method was used to compare costs and risk of hospitalisation to adjust for potential confounding factors and control for selection bias. RESULTS: We analysed 191 patients. At baseline, the 133 patients (70%) who were prescribed ONS were more disabled (p < 0.001) and had poorer perception of their health (p = 0.02), lower QoL (p = 0.04) and lower appetite (p < 0.001) than the 58 patients (30%) who were not prescribed ONS. At 6 months, appetite had improved more in the ONS prescription group (p = 0.001). Weight change was not different between groups. Patients prescribed ONS were more frequently hospitalised (OR 2.518, 95% CI: [1.088; 5.829] hosp; p = 0.03). Analyses of adjusted populations revealed no differences in health care costs between groups. In the ONS prescription group, we identified that health care costs were lower (p = 0.042) in patients with an energy intake from ONS ≥ 500 kcal/d (1389 ± 264 €) vs. < 500 kcal/d (3502 ± 839 €). The risk of hospitalisation was reduced 3 and 5 times when the intake from ONS was ≥30 g of protein/day or ≥500 kcal/d, respectively. CONCLUSIONS: ONS prescription in malnourished elderly patients generated no extra heath care cost. High energy and protein intake from ONS was associated with a reduced risk of hospitalisation and health care costs.


Assuntos
Nutrição Enteral , Serviços de Assistência Domiciliar , Hospitalização , Desnutrição/terapia , Estado Nutricional , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Envelhecimento , Regulação do Apetite , Análise Custo-Benefício , Proteínas Alimentares/administração & dosagem , Ingestão de Energia , Nutrição Enteral/efeitos adversos , Nutrição Enteral/economia , Feminino , França , Custos de Cuidados de Saúde , Serviços de Assistência Domiciliar/economia , Hospitalização/economia , Humanos , Masculino , Desnutrição/diagnóstico , Desnutrição/economia , Desnutrição/fisiopatologia , Estudos Prospectivos , Qualidade de Vida , Medição de Risco , Fatores de Risco , Fatores de Tempo , Resultado do Tratamento
6.
Rev Epidemiol Sante Publique ; 66(3): 187-194, 2018 May.
Artigo em Francês | MEDLINE | ID: mdl-29625860

RESUMO

INTRODUCTION: The Confusion Assessment Method (CAM) is a validated key tool in clinical practice and research programs to diagnose delirium and assess its severity. There is no validated French version of the CAM training manual and coding guide (Inouye SK). The aim of this study was to establish a consensual French version of the CAM and its manual. METHODS: Cross-cultural adaptation to achieve equivalence between the original version and a French adapted version of the CAM manual. RESULTS: A rigorous process was conducted including control of cultural adequacy of the tool's components, double forward and back translations, reconciliation, expert committee review (including bilingual translators with different nationalities, a linguist, highly qualified clinicians, methodologists) and pretesting. A consensual French version of the CAM was achieved. CONCLUSION: Implementation of the CAM French version in daily clinical practice will enable optimal diagnosis of delirium diagnosis and enhance communication between health professionals in French speaking countries. Validity and psychometric properties are being tested in a French multicenter cohort, opening up new perspectives for improved quality of care and research programs in French speaking countries.


Assuntos
Confusão/diagnóstico , Características Culturais , Delírio/diagnóstico , Idioma , Psicometria/métodos , Traduções , Doença Aguda , Idoso , Confusão/psicologia , Comparação Transcultural , Delírio/psicologia , Avaliação Geriátrica/métodos , Humanos , Reprodutibilidade dos Testes , Inquéritos e Questionários
7.
J Frailty Aging ; 5(4): 233-241, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27883170

RESUMO

The Région Languedoc Roussillon is the umbrella organisation for an interconnected and integrated project on active and healthy ageing (AHA). It covers the 3 pillars of the European Innovation Partnership on Active and Healthy Ageing (EIP on AHA): (A) Prevention and health promotion, (B) Care and cure, (C) and (D) Active and independent living of elderly people. All sub-activities (poly-pharmacy, falls prevention initiative, prevention of frailty, chronic respiratory diseases, chronic diseases with multimorbidities, chronic infectious diseases, active and independent living and disability) have been included in MACVIA-LR which has a strong political commitment and involves all stakeholders (public, private, patients, policy makers) including CARSAT-LR and the Eurobiomed cluster. It is a Reference Site of the EIP on AHA. The framework of MACVIA-LR has the vision that the prevention and management of chronic diseases is essential for the promotion of AHA and for the reduction of handicap. The main objectives of MACVIA-LR are: (i) to develop innovative solutions for a network of Living labs in order to reduce avoidable hospitalisations and loss of autonomy while improving quality of life, (ii) to disseminate the innovation. The three years of MACVIA-LR activities are reported in this paper.


Assuntos
Envelhecimento , Política de Saúde , Promoção da Saúde , Vida Independente , Medicina Preventiva , Acidentes por Quedas/prevenção & controle , Idoso , Idoso de 80 Anos ou mais , Doença Crônica , Comorbidade , União Europeia , França , Hospitalização , Humanos , Múltiplas Afecções Crônicas , Saúde Bucal , Autonomia Pessoal , Polimedicação , Qualidade de Vida , Doenças Respiratórias
8.
Clin Interv Aging ; 10: 491-7, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25759568

RESUMO

BACKGROUND AND PURPOSE: Musculoskeletal system deterioration among the aging is a major reason for loss of autonomy and directly affects the quality of life of the elderly. Articular evaluation is part of physiotherapeutic assessment and helps in establishing a precise diagnosis and deciding appropriate therapy. Reference instruments are valid but not easy to use for some joints. The main goal of our study was to determine reliability and intertester reproducibility of the MP-BV, an inertial sensor (the MotionPod(®) [MP]) combined with specific software (BioVal [BV]), for elbow passive range-of-motion measurements in geriatrics. METHODS: This open, monocentric, randomized study compared inertial sensor to inclinometer in patients hospitalized in an acute, post-acute, and long-term-care gerontology unit. RESULTS: Seventy-seven patients (mean age 83.5±6.4 years, sex ratio 1.08 [male/female]) were analyzed. The MP-BV was reliable for each of the three measurements (flexion, pronation, and supination) for 24.3% (CI 95% 13.9-32.8) of the patients. Separately, the percentages of reliable measures were 59.7% (49.2-70.5) for flexion, 68.8% (58.4-79.5) for pronation, and 62.3% (51.2-73.1) for supination. The intraclass correlation coefficients were 0.15 (0.07-0.73), 0.46 (0.27-0.98), and 0.50 (0.31-40 0.98) for flexion, pronation, and supination, respectively. CONCLUSION: This study shows the convenience of the MP-BV in terms of ease of use and of export of measured data. However, this instrument seems less reliable and valuable compared to the reference instruments used to measure elbow range of motion in gerontology.


Assuntos
Articulação do Cotovelo/fisiologia , Amplitude de Movimento Articular/fisiologia , Idoso de 80 Anos ou mais , Feminino , Geriatria/instrumentação , Geriatria/métodos , Humanos , Masculino , Variações Dependentes do Observador , Reprodutibilidade dos Testes
9.
J Nutr Health Aging ; 19(3): 250-7, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25732208

RESUMO

Frailty is a geriatric syndrome that predicts disability, morbidity and mortality in the elderly. Poor nutritional status is one of the main risk factors for frailty. Macronutrients and micronutrients deficiencies are associated with frailty. Recent studies suggest that improving nutritional status for macronutrients and micronutrients may reduce the risk of frailty. Specific diets such as the Mediterranean diet rich in anti-oxidants, is currently investigated in the prevention of frailty. The aim of this paper is to summarize the current body of knowledge on the relations between nutrition and frailty, and provide recommendations for future nutritional research on the field of frailty.


Assuntos
Idoso Fragilizado , Estado Nutricional , Idoso , Dieta Mediterrânea , Ingestão de Energia , Idoso Fragilizado/estatística & dados numéricos , Humanos , Micronutrientes/deficiência , Fatores de Risco , Deficiência de Vitamina D/epidemiologia
10.
J Nutr Health Aging ; 19(2): 234-9, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25651452

RESUMO

INTRODUCTION: Cobalamin deficiency is frequent in elderly patients and the main aetiologies are food-cobalamin malabsorption and pernicious anaemia. The aim of our retrospective study was to identify the causes and methods of management of cobalamin deficiency at Nice geriatric university hospital. METHODS: A retrospective monocentric study was conducted over 14 months at Nice geriatric hospital, which included patients with cobalamin deficiency having received supplementation. The clinical and paraclinical data, etiological diagnosis, treatment and follow-up modalities were analyzed retrospectively. RESULTS: We studied 125 elderly patients whose median age was 85.5 ± 7 years. The etiological diagnosis was food-cobalamin malabsorption for 72 patients (57.6 %), nutritional cobalamin deficiency for 15 patients (12 %), pernicious anaemia for 12 patients (9.6 %) and there was no etiological diagnosis for 26 patients (20.8 %). Concerning cobalamin therapy, 111 patients (88.8 %) received oral therapy and 14 (11.2 %) intramuscular therapy. Vitamin B12 levels increased significantly after supplementation (p<0.001) but cobalamin administration varied according to the diagnoses (p<0.001) and was less effective in patients with dementia (p=0.04) and food-cobalamin malabsorption. CONCLUSION: Our study showed the importance of food-cobalamin malabsorption in etiological diagnosis in accordance with the literature, but also the non-negligible share of nutritional cobalamin deficiency. Mainly oral cobalamin supplementation was used in our study with a significant increase in vitamin B12 levels. An oral cobalamin regimen is proposed for elderly patients with cobalamin deficiency but with no severe neurological signs.


Assuntos
Geriatria , Hospitais Universitários , Deficiência de Vitamina B 12/etiologia , Deficiência de Vitamina B 12/terapia , Vitamina B 12/uso terapêutico , Absorção Fisiológica , Administração Oral , Idoso , Idoso de 80 Anos ou mais , Anemia Perniciosa/complicações , Demência/complicações , Suplementos Nutricionais , Feminino , Alimentos , França , Humanos , Injeções Intramusculares , Síndromes de Malabsorção/complicações , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Vitamina B 12/administração & dosagem , Deficiência de Vitamina B 12/sangue , Deficiência de Vitamina B 12/diagnóstico
11.
J Nutr Health Aging ; 17(4): 402-12, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23538667

RESUMO

BACKGROUND: The prevalence of vitamin D insufficiency is very high in the nursing home (NH) population. Paradoxically, vitamin D insufficiency is rarely treated despite of strong clinical evidence and recommendations for supplementation. This review aims at reporting the current knowledge of vitamin D supplementation in NH and proposing recommendations adapted to the specificities of this institutional setting. DESIGN: Current literature on vitamin D supplementation for NH residents was narratively presented and discussed by the French Group of Geriatrics and Nutrition. RESULT: Vitamin D supplementation is a safe and well-tolerated treatment. Most residents in NH have vitamin D insufficiency, and would benefit from vitamin D supplement. However, only few residents are actually treated. Current specific and personalized protocols for vitamin D supplementation may not be practical for use in NH settings (e.g., assessment of serum vitamin D concentrations before and after supplementation). Therefore, our group proposes a model of intervention based on the systematic supplementation of vitamin D (1,000 IU/day) since the patient's admission to the NH and throughout his/her stay without the need of a preliminary evaluation of the baseline levels. Calcium should be prescribed only in case of poor dietary calcium intake. CONCLUSION: A population-based rather than individual-based approach may probably improve the management of vitamin D insufficiency in the older population living in NH, without increasing the risks of adverse health problems. The clinical relevance and cost effectiveness of this proposal should be assessed under NH real-world conditions to establish its feasibility.


Assuntos
Suplementos Nutricionais , Instituição de Longa Permanência para Idosos , Casas de Saúde , Deficiência de Vitamina D/tratamento farmacológico , Deficiência de Vitamina D/epidemiologia , Vitamina D/administração & dosagem , Idoso , Cálcio da Dieta/administração & dosagem , Cálcio da Dieta/sangue , Avaliação Geriátrica , Humanos , Estado Nutricional , Guias de Prática Clínica como Assunto , Vitamina D/sangue , Deficiência de Vitamina D/sangue
12.
Strahlenther Onkol ; 188(5): 383-7, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22410833

RESUMO

BACKGROUND: Rectal cancer in patients aged ≥ 80 years is increasingly more frequent. Little is known regarding their clinical history and outcome after treatment. This retrospective study was undertaken to provide data on this situation. MATERIAL AND METHOD: A questionnaire was sent to the medical doctors of 414 patients listed in the database of Régime Général of Sécurité Sociale, living in the Provence-Alpes-Côte d'Azur (PACA) region between 2002 and 2005, aged ≥ 80 years, and registered as having rectal cancer. Survival was analyzed and correlated with patients' and treatment characteristics. RESULTS: Validated questionnaire was available for 78 patients representing close to 20% of the PACA-targeted population. The majority of patients presented a T3 tumor treated with surgery (61 cases). Median follow-up for the 78 patients was 42 months and the 5-year overall survival was 51%. In the multivariate analysis, the main prognostic factors were gender (better survival in women), age ≤ 85 years, and most of all performance of surgery. CONCLUSION: Rectal cancer for patients between 79 and 85 years does not differ much from that in younger patients and can be treated in a similar manner--depending on the patient's general condition. In patients > 85 years, it is advisable to reduce surgical trauma as much as possible.


Assuntos
Neoplasias Retais/mortalidade , Idoso de 80 Anos ou mais , Feminino , França , Humanos , Masculino , Análise Multivariada , Prognóstico , Neoplasias Retais/patologia , Estudos Retrospectivos , Fatores de Risco , Inquéritos e Questionários , Análise de Sobrevida , Resultado do Tratamento
13.
Rev Epidemiol Sante Publique ; 58(3): 181-7, 2010 Jun.
Artigo em Francês | MEDLINE | ID: mdl-20430554

RESUMO

BACKGROUND: Given the serious health effects of lead poisoning (Pb> or =10microg/dL), the present study was designed to estimate the time required to reach and identify factors associated with reaching Pb<10microg/dL according to the severity of the poisoning. METHODS: Since 1992, the Greater Paris lead poisoning monitoring system (SSSILF) has been systematically recording data on blood lead levels of screening and follow-up testing of children in the region. In children under the age of seven when screened positive for lead poisoning, survival curves without reaching the threshold of 10microg/dL and the relative risk (RR) of reaching this threshold were calculated (Kaplan-Meier curves and Cox model), according to blood lead level groups (Group 4: Pb> or =45microg/dL; Group 3: 25microg/dL< or =Pb<45microg/dL; Group 2: 10microg/dL< or =Pb<25microg/dL; (by definition, Group 1: Pb<100microg/L and risk factors of poisoning). RESULTS: The median survival times without reaching the threshold of Pb<10microg/dL were 72.7 months for Group 4, 36.8 months for Group 3 and 14.5 months for Group 2. Compared to reference categories, the time to Pb<10microg/dL was longer for children aged four and over at the time they screened positive for poisoning (Groups 4 and 3), for children displaying pica behavior (Groups 3 and 2), for children in an environment with another child suffering from lead poisoning (Groups 3 and 2) and for children of mothers from Sub-Saharan or North Africa countries (Group 2); the differences reached statistical significance. Changes in Pb levels were better for all children (Groups 4, 3 and 2) screened over the most recent period, i.e. 2002 to 2006, and for Group 2 children living in Paris or the nearby district of Seine-Saint-Denis. CONCLUSION: While the time required has gone down over recent years, the time to reach the threshold of Pb<10microg/dL is counted in years and varies depending on known poisoning risk factors and the district responsible for patient management. It is essential to have early lead poisoning screening for children in high-risk groups and then follow-up after rapid implementation of appropriate medical and social measures.


Assuntos
Chumbo/sangue , Fatores Etários , Quelantes/uso terapêutico , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Estimativa de Kaplan-Meier , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/mortalidade , Intoxicação por Chumbo/terapia , Masculino , Fatores Sexuais
14.
J Nutr Health Aging ; 14(2): 110-20, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20126959

RESUMO

This paper aims to define the role of the primary care physician (PCP) in the management of Alzheimer's disease (AD) and to propose a model for a work plan. The proposals in this position paper stem from a collaborative work of experts involved in the care of AD patients. It combines evidence from a literature review and expert's opinions who met in Paris, France, on July 2009 during the International Association of Geriatrics and Gerontology (IAGG) World Congress. The PCP's intervention appears essential at many levels: detection of the onset of dementia, diagnostic management, treatment and follow-up. The key role of the PCP in the management of AD, as care providers and care planners, is consolidated by the family caregiver's confidence in their skills. In primary care practice the first step is to identify dementia. The group proposes a "case finding" strategy, in target situations in which dementia should be detected to allow, secondarily, a diagnosis of AD, in certain cases. We propose that the PCP identifies 'typical' cases. In typical cases, among older subjects, the diagnosis of "probable AD" can be done by the PCP and then confirm by the specialist. While under-diagnosis of AD exists, so does under-disclosure. Disclosure to patient and family should be done by both specialist and PCP. Then, the PCP has a central role in management of the disease with the general objectives to detect, prevent and treat, when possible, the complications of the disease (falls, malnutrition, behavioural and psychological symptoms of dementia). The PCP needs to give basic information to the caregiver on respite care and home support services in order to prevent crisis situations such as unplanned institutionalisation and "emergency" hospital admission. Finally, therapeutic research must be integrated in the daily practice of PCP. It is a matter of patients' right to benefit from access to innovation and clinical research whatever his age or diseases, while of course fully respecting the rules and protective measures that are in force.


Assuntos
Doença de Alzheimer/diagnóstico , Doença de Alzheimer/terapia , Serviços de Saúde para Idosos/normas , Papel do Médico , Atenção Primária à Saúde/normas , Competência Clínica , Diagnóstico Precoce , Humanos , Comunicação Interdisciplinar , Administração dos Cuidados ao Paciente , Equipe de Assistência ao Paciente , Qualidade da Assistência à Saúde , Sociedades
15.
Cancer Radiother ; 13(6-7): 606-8, 2009 Oct.
Artigo em Francês | MEDLINE | ID: mdl-19699674

RESUMO

The problem of the oncogeriatrics is a real challenge for next decades. More than 60% of the patients presenting a cancer in France are more than 65 years old. Indeed, the care services of the old patients affected by cancer require skills of both medical disciplines: geriatrics and oncology. It requires a culture sharing between these two fundamentally transverse specialities. A lot of progresses have to be made, even if this stake has really been considered in our country, in particular because of the implementation of a unique oncogeriatics organization within the French National Cancer Institute (INCA), but also by the structuring of a workgroup within the French Society of Geriatrics and Gerontology.


Assuntos
Geriatria/métodos , Neoplasias/epidemiologia , Academias e Institutos , Idoso , França/epidemiologia , Avaliação Geriátrica/métodos , Geriatria/tendências , Humanos , Oncologia/métodos , Oncologia/tendências , Sociedades Médicas
16.
J Cancer Res Clin Oncol ; 134(1): 51-7, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17593391

RESUMO

PURPOSE: Physiological and molecular findings indicate over-expression of HER proteins and dysregulation of neo-angiogenesis during progression of advanced prostate cancer. The aim of this study was to test a novel rational therapeutic approach by combining docetaxel with an EGFR-targeting agent (cetuximab) and with an anti-angiogenic agent (sunitinib, SUTENT). METHODS: Mice bearing well-established PC3 prostate tumors (mean tumor volume/treatment group approximately 250 mm(3)) were treated every week with vehicle alone (controls), sunitinib (40 mg/kg/day, 5 days/week for 3 weeks, 0.2 ml p.o.), cetuximab (0.2 mg/kg/day, 5 days/week for 3 weeks, 0.2 ml i.p.) and docetaxel (10 mg/kg, 1 day/week for 3 weeks, 0.2 ml i.p.). RESULTS: Each drug, administered as a single-agent, demonstrated comparable and moderate effects on tumor growth with approximately 50 % inhibition at the end of the 3-week dosing schedule. Computed combination ratio (CR) values for tumor growth determined on days 61, 68 and 75 after cell implantation indicated supra-additive effects for the sunitinib-docetaxel (1.53, 1.15 and 1.47, respectively) and sunitinib-cetuximab combinations (1.2, 1.32 and 1.14, respectively), and suggested additive effects only for the sunitinib-cetuximab-docetaxel combination (CR = 1). The effects on tumor growth were accompanied by a parallel diminution in tumor cell proliferation (Ki 67) and tumor vascularization (von Willebrandt factor). There were significantly higher pro-apoptotic effects (caspase-3 cleavage) observed for the sunitinib-docetaxel and sunitinib-docetaxel-cetuximab as compared to the other conditions. CONCLUSION: The supra-additive anti-tumor effect observed with the sunitinib-docetaxel combination might support innovative strategies in the management of advanced prostate cancer.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Neoplasias Hormônio-Dependentes/tratamento farmacológico , Neoplasias da Próstata/tratamento farmacológico , Animais , Anticorpos Monoclonais/administração & dosagem , Anticorpos Monoclonais Humanizados , Biomarcadores Tumorais/genética , Biomarcadores Tumorais/metabolismo , Proliferação de Células , Cetuximab , Docetaxel , Perfilação da Expressão Gênica , Humanos , Indóis/administração & dosagem , Masculino , Camundongos , Camundongos Nus , Neoplasias Hormônio-Dependentes/secundário , Antígeno Prostático Específico/sangue , Neoplasias da Próstata/patologia , Pirróis/administração & dosagem , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Sunitinibe , Taxa de Sobrevida , Taxoides/administração & dosagem , Células Tumorais Cultivadas/efeitos dos fármacos , Ensaios Antitumorais Modelo de Xenoenxerto
17.
J Nutr Health Aging ; 11(1): 38-48, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17315079

RESUMO

Weight loss, together with psychological and behavioural symptoms and problems of mobility, is one of the principal manifestations of Alzheimer's disease (AD). Weight loss may be associated with protein and energy malnutrition leading to severe complications (alteration of the immune system, muscular atrophy, loss of independence). Various explanations have been proposed such as atrophy of the mesial temporal cortex, biological disturbances, or feeding behaviours; however, none has been proven. Prevention of weight loss in AD is a major issue. It requires regular follow-up and must be an integral part of the care plan. The aim of this article is to review the present state of scientific knowledge on weight loss associated with AD. We will consider four points: the natural history of weight loss, its known etiological factors, its consequences and the various management options.


Assuntos
Doença de Alzheimer/fisiopatologia , Metabolismo Energético/fisiologia , Fenômenos Fisiológicos da Nutrição , Redução de Peso , Córtex Cerebral/patologia , Humanos , Estado Nutricional
19.
J Oncol Pharm Pract ; 12(2): 69-73, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16984744

RESUMO

BACKGROUND: Recent advances in the molecular biology and genetics of colorectal cancer have led to the identification of potential therapeutic targets such as epidermal growth factor receptor, vascular endothelial growth factor and endothelial receptors. OBJECTIVE: This review will examine the major therapeutic advances along with the preclinical basis justifying their combination with conventional therapeutic tools. This review will also critically consider current possibilities offered to identify responding patients. DATA SOURCES: Preclinical and primary clinical trial results published in peer-review journals. The authors examined the relevance and subsequent inclusion of the data. CONCLUSIONS: Cetuximab and bevacizumab provide new benefits in terms of the response rate and survival. There remain, however, important questions concerning, for instance, optimal combinations between conventional cytotoxic agents and targeted therapies and also between targeted drugs themselves. These new targeted treatments are costly and in this context the question of the identification of the right drug for the right patient is particularly relevant. Adequate tools in predicting the efficacy of targeted treatments are still needed.


Assuntos
Antineoplásicos/uso terapêutico , Neoplasias Colorretais/tratamento farmacológico , Fator A de Crescimento do Endotélio Vascular/antagonistas & inibidores , Inibidores da Angiogênese/uso terapêutico , Neoplasias Colorretais/metabolismo , Humanos
20.
J Nutr Health Aging ; 9(2): 81-4, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15791350

RESUMO

OBJECTIVES: Weight loss and malnutrition are frequent and serious complications of Alzheimer's disease. The aim of the present article was to describe the cognitive and behavioural characteristics of the test population within the frame of the PHRC REAL.FR cohort (for Réseau sur la Maladie d'Alzheimer Français), depending on their nutritional state, and to consider their evolution one year after the original inclusion. METHOD: The study population' stratification was done in three groups according to their Mini Nutritional Assessment (MNA) score: malnutrition group (MNA < 17.5), at risk of malnutrition group (MNA 17.5-23.5), and normal nutritional status group (MNA > or = 23.5). 561 patients were evaluated at inclusion time, 393 at one year. The evaluation included the following scales: Mini Nutritional Assessment (MNA), Mini Mental State Examination (MMSE), Activities Daily Living (ADL), Instrumental Activities Daily Living (IADL), Neuro Psychiatric Inventory (NPI) and Zarit scale (ZARIT). Comparison and descriptive analysis for each MNA group at baseline and at one year has been performed. RESULTS: at baseline, the well-nourished and the malnutrition risk groups are significantly different concerning age, IADL and NPI; the well-nourished and undernutrition groups are different concerning MMSE, NPI and Zarit; the malnutrition risk and undernutrition groups are only different concerning NPI. At one year, the well-nourished and the malnutrition risk and undernutrition groups are different concerning one lonely variable, the NPI, in a significant way. The comparison of the three groups between baseline and one-year evaluation demonstrate for the well-nourished group an aggravation of MMSE, ADL, IADL, NPI, for the malnutrition risk group of MMSE and IADL, and for the undernutrition group of MMSE, IADL and NPI. CONCLUSION: Among the patients suffering from Alzheimer's disease, the most malnutritioned worsen highly on cognitive and functional capacities. Furthermore, the nutritional aggravation seems strongly linked to behavioural disorders aggravation. The improvement of those disorders has therefore to be part of every improvement strategy applied to the nutritional status of the demented patients.


Assuntos
Doença de Alzheimer/fisiopatologia , Estado Nutricional , Redução de Peso , Atividades Cotidianas , Idoso , Doença de Alzheimer/complicações , Humanos , Desnutrição/complicações , Testes Neuropsicológicos , Avaliação Nutricional , Fatores de Risco
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