18 results on '"MESH: Survivors"'
Search Results
2. Late thyroid complications in survivors of childhood acute leukemia. An LEA study
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Gérard Michel, Marie-Dominique Tabone, Jean-Hugues Dalle, Dominique Plantaz, P Chastagner, Vincent Barlogis, Patrick Lutz, Pascal Auquier, Julie Berbis, Claire Oudin, Maryline Poiree, André Baruchel, Sandrine Thouvenin, Justyna Kanold, Yves Bertrand, Stéphane Ducassou, Virginie Villes, Guy Leverger, Anne Sirvent, Virginie Gandemer, Service d'hématologie pédiatrique, Université de la Méditerranée - Aix-Marseille 2-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE), Santé Publique et maladies Chroniques : Qualité de vie Concepts, Usages et Limites, Déterminants (SPMC), Assistance Publique - Hôpitaux de Marseille (APHM)-Aix Marseille Université (AMU), Hématologie et immunologie pédiatrique, Hospices Civils de Lyon (HCL)-CHU Lyon-Institut d'hématologie et d'oncologie pédiatrique [CHU - HCL] (IHOPe), Hospices Civils de Lyon (HCL)-Hôpital Femme-Mère-Enfant (HFME), CHU Clermont-Ferrand-CIC Inserm 501, Service de Pédiatrie, Unité d'Oncologie et Hématologie Pédiatrique, Centre Hospitalier Universitaire de Nice (CHU Nice), Hôpital Pellegrin Tripode, Service Hématologie Infantile, CHU Grenoble, Service d'hématologie-immunologie-oncologie pédiatrique [CHU Trousseau], Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Hôpital Robert Debré Paris, Hôpital Robert Debré, Institut de Génétique et Développement de Rennes (IGDR), Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), CHU Pontchaillou [Rennes], Service de pédiatrie, Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble, Pédiatrie et oncologie pédiatrique [Hôpital de la Timone - APHM], Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE), Service d'hématologie et immunologie pédiatrique, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré-Université Paris Diderot - Paris 7 (UPD7), Hôpital Trousseau, Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), French National Clinical Research Program, French National Cancer Institute (InCA), French National Research Agency (ANR), Canceropole PACA, Regional Council PACA, Herault Departmental Comity of the Ligue Contre le Cancer, French Institute for Public Health Research (IRESP), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-CHU Trousseau [APHP], Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Université Paris Diderot - Paris 7 (UPD7)-Hôpital Robert Debré-Assistance publique - Hôpitaux de Paris (AP-HP) (APHP), CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), and Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
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Male ,MESH: Therapy/adverse effects ,[SHS.PSY]Humanities and Social Sciences/Psychology ,Gastroenterology ,0302 clinical medicine ,Risk Factors ,MESH: Risk Factors ,MESH: Child ,Prevalence ,Cumulative incidence ,Survivors ,MESH: Incidence ,Child ,Thyroid cancer ,MESH: Combined Modality ,MESH: Survivors ,Acute leukemia ,Leukemia ,MESH: Thyroid Diseases/diagnosis ,MESH: France/epidemiology ,Incidence ,Thyroid ,Hematology ,MESH: Follow-Up Studies ,Total body irradiation ,[SHS.ECO]Humanities and Social Sciences/Economics and Finance ,Combined Modality Therapy ,MESH: Leukemia/complications ,3. Good health ,medicine.anatomical_structure ,Child, Preschool ,030220 oncology & carcinogenesis ,Acute Disease ,MESH: Acute Disease ,Female ,France ,Thyroid function ,medicine.medical_specialty ,MESH: Leukemia/epidemiology ,MESH: Combined Modality Therapy/methods ,MESH: Leukemia/therapy ,MESH: Thyroid Diseases/epidemiology ,Article ,MESH: Multivariate Analysis ,03 medical and health sciences ,Internal medicine ,MESH: Thyroid Diseases/etiology ,medicine ,Humans ,MESH: Prevalence ,MESH: Humans ,business.industry ,MESH: Child, Preschool ,medicine.disease ,Thyroid Diseases ,MESH: Male ,Surgery ,Transplantation ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,Multivariate Analysis ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,Prophylactic cranial irradiation ,business ,MESH: Female ,Follow-Up Studies ,030215 immunology - Abstract
International audience; Thyroid complications are known side effects of irradiation. However, the risk of such complications in childhood acute leukemia survivors who received either central nervous system irradiation or hematopoietic stem cell transplantation is less described. We prospectively evaluated the incidence and risk factors for thyroid dysfunction and tumors in survivors of childhood acute myeloid or lymphoid leukemia. A total of 588 patients were evaluated for thyroid function, and 502 individuals were assessed for thyroid tumors (median follow-up duration: 12.6 and 12.5 years, respectively). The cumulative incidence of hypothyroidism was 17.3% (95% CI: 14.1-21.1) and 24.6% (95% CI: 20.4-29.6) at 10 and 20 years from leukemia diagnosis, respectively. Patients who received total body irradiation (with or without prior central nervous system irradiation) were at higher risk of hypothyroidism (adjusted HR: 2.87; P=0.04 and 2.79, P=0.01, respectively) as compared with transplanted patients who never received any irradiation. Patients transplanted without total body irradiation who received central nervous system irradiation were also at higher risk (adjusted HR: 3.39; P=0.02). Patients irradiated or transplanted at older than 10 years of age had a lower risk (adjusted HR: 0.61; P=0.02). Thyroid malignancy was found in 26 patients (5.2%). Among them, two patients had never received any type of irradiation: alkylating agents could also promote thyroid cancer. The cumulative incidence of thyroid malignancy was 9.6% (95% CI: 6.0-15.0) at 20 years. Women were at higher risk than men (adjusted HR: 4.74; P=0.002). In conclusion, thyroid complications are frequent among patients who undergo transplantation after total body irradiation and those who received prior central nervous system irradiation. Close monitoring is thus warranted for these patients. Clinicaltrials.gov identifier: NCT 01756599.
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- 2016
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3. Meta-Analysis on the Use of Zidovudine and Interferon-Alfa in Adult T-Cell Leukemia/Lymphoma Showing Improved Survival in the Leukemic Subtypes
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William J. Harrington, Yves Plumelle, Olivier Hermine, Graham P. Taylor, Juan Carlos Ramos, Patricia Tortevoye, Antoine Gessain, Gérard Panelatti, Ali Bazarbachi, Zaher K. Otrock, Pathologie et virologie moléculaire ( PVM ), Université Paris Diderot - Paris 7 ( UPD7 ) -Centre National de la Recherche Scientifique ( CNRS ), Service d'Hematologie Biologique, CHU Fort de France, Imperial College London, Cytokines, hématopoïèse et réponse immune ( CHRI ), Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), American University of Beirut [Beyrouth] (AUB), CHU de la Martinique [Fort de France], University of Miami [Coral Gables], Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Départment d'Hématologie, Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Pathologie et virologie moléculaire (PVM (UMR_7151)), Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Cytokines, hématopoïèse et réponse immune (CHRI), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Pathologie et virologie moléculaire (PVM), and Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS)
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Male ,Oncology ,Cancer Research ,Time Factors ,MESH: Chi-Square Distribution ,viruses ,Kaplan-Meier Estimate ,MESH: Risk Assessment ,MESH: Proportional Hazards Models ,MESH: Aged, 80 and over ,0302 clinical medicine ,Risk Factors ,MESH: Martinique ,MESH: Risk Factors ,immune system diseases ,hemic and lymphatic diseases ,Antineoplastic Combined Chemotherapy Protocols ,Mogamulizumab ,Leukemia-Lymphoma, Adult T-Cell ,Medicine ,Survivors ,MESH: Kaplan-Meiers Estimate ,MESH: Leukemia-Lymphoma, Adult T-Cell ,ComputingMilieux_MISCELLANEOUS ,MESH: Treatment Outcome ,Aged, 80 and over ,MESH: Aged ,MESH: Survivors ,0303 health sciences ,MESH: Middle Aged ,MESH: Zidovudine ,Middle Aged ,3. Good health ,MESH: Antineoplastic Combined Chemotherapy Protocols ,Leukemia ,Treatment Outcome ,[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology ,MESH: Young Adult ,030220 oncology & carcinogenesis ,MESH: Great Britain ,Female ,MESH: Interferon-alpha ,Zidovudine ,Martinique ,medicine.drug ,Adult ,MESH: Antiviral Agents ,medicine.medical_specialty ,Adolescent ,Alpha interferon ,Antiviral Agents ,Risk Assessment ,Adult T-cell leukemia/lymphoma ,Young Adult ,03 medical and health sciences ,[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathology ,Internal medicine ,MESH: United States ,Humans ,Interferon alfa ,Aged ,Proportional Hazards Models ,Retrospective Studies ,030304 developmental biology ,MESH: Adolescent ,Chi-Square Distribution ,MESH: Humans ,business.industry ,MESH: Time Factors ,Interferon-alpha ,MESH: Adult ,MESH: Retrospective Studies ,medicine.disease ,United Kingdom ,United States ,MESH: Male ,Lymphoma ,Immunology ,business ,MESH: Female ,[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology - Abstract
Purpose Human T-cell lymphotropic virus type-I–associated adult T-cell leukemia/lymphoma (ATL) is an aggressive, chemotherapy-resistant malignancy. Multiple small studies using zidovudine (AZT) and interferon-alfa (IFN-α) have shown response in patients with ATL. However, the impact of this innovative antiviral treatment strategy on long-term survival remains undetermined. Patients and Methods We report a meta-analysis of antiviral therapy of ATL. Medical records of 254 patients with ATL who were treated in the United States, the United Kingdom, Martinique, and continental France were individually reviewed. Results According to Shimoyama classification, there were 116 patients with acute ATL, 18 patients with chronic ATL, 11 patients with smoldering ATL, and 100 patients with ATL lymphoma. In 231 patients with available survival data, first-line therapy was recorded in 207 patients. Five-year overall survival rates were 46% for 75 patients who received first-line antiviral therapy (P = .004), 20% for 77 patients who received first-line chemotherapy, and 12% for 55 patients who received first-line chemotherapy followed by antiviral therapy. Patients with acute, chronic, and smoldering ATL significantly benefited from first-line antiviral therapy, whereas patients with ATL lymphoma experienced a better outcome with chemotherapy. In acute ATL, achievement of complete remission with antiviral therapy resulted in 82% 5-year survival. Antiviral therapy in chronic and smoldering ATL resulted in 100% 5-year survival. Multivariate analysis confirmed that first-line antiviral therapy significantly improves overall survival of patients with ATL (hazard ratio, 0.47; 95% CI, 0.27 to 0.83; P = .021). Conclusion These results confirm the high efficacy of AZT and IFN, which should now be considered the gold standard first-line therapy in leukemic subtypes of ATL.
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- 2010
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4. Positive and cost-effectiveness effect of spa therapy on the resumption of occupational and non-occupational activities in women in breast cancer remission: a French multicentre randomised controlled trial
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Charline Mourgues, Anne Leger-Enreille, Marie Blanquet, Laurent Gerbaud, Candy Auclair, Stéphanie Léger, Fabrice Kwiatkowski, Yves-Jean Bignon, Fleur Peyrol, Institut Pascal (IP), and SIGMA Clermont (SIGMA Clermont)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS)
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MESH: Remission Induction ,MESH: Massage ,Cost effectiveness ,Spa therapy ,Cost-Benefit Analysis ,Non occupational ,Relaxation Therapy ,law.invention ,Breast cancer ,Randomized controlled trial ,Occupational Therapy ,law ,Activities of Daily Living ,Survivors ,health care economics and organizations ,2. Zero hunger ,Massage ,Randomised controlled trial ,MESH: Survivors ,MESH: Aged ,Work resumption ,MESH: Middle Aged ,Oncology (nursing) ,Remission Induction ,General Medicine ,Middle Aged ,University hospital ,3. Good health ,Oncology ,MESH: Diet Therapy ,Female ,France ,Adult ,medicine.medical_specialty ,Breast Neoplasms ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Steam Bath ,Intervention (counseling) ,medicine ,Humans ,Contraindication ,Aged ,MESH: Occupational Therapy ,MESH: Humans ,business.industry ,MESH: Activities of Daily Living ,MESH: Steam Bath ,MESH: Adult ,medicine.disease ,MESH: France ,Physical therapy ,MESH: Relaxation Therapy ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business ,Body mass index ,MESH: Female ,MESH: Breast Neoplasms ,Diet Therapy ,MESH: Cost-Benefit Analysis - Abstract
Purpose of the research The main aim was to assess the effects of a spa treatment on the resumption of occupational and non-occupational activities and the abilities of women in breast cancer remission. A cost-effectiveness analysis (CEA) was also performed. Methods and sample A multicentre randomised controlled trial was carried out between 2008 and 2010 in the University Hospital of Auvergne and two private hospitals in Clermont-Ferrand, France. Eligible patients were women in complete breast cancer remission without contraindication for physical activities or cognitive disorders and a body mass index between 18.5 and 40 kg/m 2 . The intervention group underwent spa treatment combined with consultation with dietician whereas the control underwent consultations with the dietician only. Of the 181 patients randomised, 92 and 89 were included in the intervention and the control groups, respectively. The CEA involved 90 patients, 42 from the intervention group and 48 from the control group. Key results The main results showed a higher rate of resumption of occupational activities in the intervention group ( p = 0.0025) and a positive effect of the intervention on the women's ability to perform occupational activities 12 months after the beginning of the study ( p = 0.0014), and on their ability to perform family activities ( p = 0.033). The stay in a thermal centre was cost-effective at 12 months. Conclusions Spa treatment is a cost-effective strategy to improve resumption of occupational and non-occupational activities and the abilities of women in breast cancer remission.
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- 2014
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5. Childhood cancer survival in France, 2000–2008
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Aurélie Guyot-Goubin, Brigitte Lacour, Emmanuel Desandes, Sandra Guissou, Jacqueline Clavel, Stéphanie Goujon, Solène Desmée, Registre National des Tumeurs Solides de l'Enfant (RNTSE), Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Cancéropôle du Grand Est, Centre de recherche en épidémiologie et santé des populations (CESP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Sud - Paris 11 (UP11)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Registre National des Hémopathies malignes de l'Enfant (RNHE), and Institut de Veille Sanitaire (INVS)-Institut National de la Santé et de la Recherche Médicale (INSERM)
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Male ,Oncology ,Ependymoma ,Cancer Research ,Time Factors ,Myeloid ,MESH: Registries ,Epidemiology ,0302 clinical medicine ,Neoplasms ,MESH: Child ,MESH: Neoplasms ,Registries ,Survivors ,MESH: Incidence ,Child ,MESH: Survivors ,0303 health sciences ,Relative survival ,Incidence ,Incidence (epidemiology) ,MESH: Infant, Newborn ,Astrocytoma ,MESH: Follow-Up Studies ,Prognosis ,MESH: Infant ,3. Good health ,Survival Rate ,medicine.anatomical_structure ,Child, Preschool ,030220 oncology & carcinogenesis ,Female ,France ,medicine.medical_specialty ,Adolescent ,MESH: Survival Rate ,MESH: Prognosis ,03 medical and health sciences ,Internal medicine ,medicine ,Humans ,Adverse effect ,030304 developmental biology ,MESH: Adolescent ,MESH: Humans ,business.industry ,MESH: Time Factors ,MESH: Child, Preschool ,Infant, Newborn ,Public Health, Environmental and Occupational Health ,Infant ,Cancer ,medicine.disease ,MESH: Male ,Clinical trial ,MESH: France ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business ,MESH: Female ,Follow-Up Studies - Abstract
International audience; This paper reports the latest survival data for French childhood cancer patients at the national level. Data from the two French National Registries of Childhood Cancer (Haematopoietic Malignancies and Solid Tumours) were used to describe survival outcomes for 15,479 children diagnosed with cancer between 2000 and 2008 in mainland France. The overall survival was 91.7% at 1 year, 86.9% at 2 years and 81.6% at 5 years. Relative survival did not differ from overall survival even for infants. Survival was lower among infants for lymphoblastic leukaemia and astrocytoma, but higher for neuroblastoma. For all cancers considered together, 5-year survival increased from 79.5% in the first (2000-2002) diagnostic period to 83.2% in the last (2006-2008) period. The improvement was significant for leukaemia, both myeloid and lymphoid, central nervous system tumours (ependymoma) and neuroblastoma. The results remained valid in the multivariate analysis, and, for all cancers combined, the risk of death decreased by 20% between 2000-2002 and 2006-2008. The figures are consistent with various international estimates and are the result of progress in treatment regimens and collaborative clinical trials. The challenge for the French registries is now to study the long-term follow-up of survivors to estimate the incidence of long-term morbidities and adverse effects of treatments.
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- 2014
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6. Prédicteurs de qualité de vie à long terme dans le cancer du sein
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Brunault , Paul, Toledano , Alain, Aguerre , Colette, Suzanne , Isabelle, Garaud , Pascal, Trzepidur-Edom , Magdalena, Calais , Gilles, Camus , Vincent, Clinique Psychiatrique Universitaire [Tours], CHRU Tours, Oncologie Radiothérapie, Clinique Hartmann - Hôpital américain de paris, Psychologie des âges de la vie ( PAVeA ), Université de Tours, Clinique d'Oncologie et de Radiothérapie [Tours] ( CORAD ), Hôpital Bretonneau-CHRU Tours, Imagerie et cerveau, Université de Tours-Institut National de la Santé et de la Recherche Médicale ( INSERM ), Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Psychologie des âges de la vie et adaptation (PAVeA), Université de Tours (UT), Clinique d'Oncologie et de Radiothérapie [Tours] (CORAD), Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)-Hôpital Bretonneau, Imagerie et cerveau (iBrain - Inserm U1253 - UNIV Tours ), Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM), and Université de Tours-Institut National de la Santé et de la Recherche Médicale (INSERM)
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MESH : Esthetics ,MESH: Radiotherapy ,MESH: breast cancer ,MESH: Depression ,MESH : Survivors ,[ SDV.MHEP.PSM ] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH : Analysis of Variance ,MESH : Breast Neoplasms ,MESH : Anxiety ,MESH: long-term survivors ,MESH : long-term survivors ,MESH : Depression ,MESH: Analysis of Variance ,MESH : Female ,MESH : Middle Aged ,MESH : France ,MESH: Chemoradiotherapy ,MESH: Survivors ,MESH: Humans ,MESH: Middle Aged ,MESH: Anxiety ,MESH : Radiotherapy ,MESH : Humans ,MESH: Quality of Life ,MESH : Follow-Up Studies ,MESH: Follow-Up Studies ,MESH : Quality of Life ,MESH : Chemoradiotherapy ,humanities ,MESH : breast cancer ,MESH: France ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH: Esthetics ,MESH: Female ,MESH: Breast Neoplasms - Abstract
International audience; INTRODUCTION: This study aimed to assess the impact of late treatment toxicity (especially radiotherapy toxicity), chemoradiotherapy treatment type (concurrent or sequential), depression and anxiety on overall, physical and emotional quality of life (QoL) in long-term breast cancer survivors. Method. We assessed 117 patients (mean follow-up since the end of treatment = 8.1 years) for late radiotherapy toxicity (LENT-SOMA scale), patient and doctor ratings of breast cosmetic outcomes, QoL (EORTC QLQ-C30), depression and anxiety (Hospital and Anxiety Depression scale). RESULTS: In univariate analyses, factors associated with significantly decreased QoL were: use of sequential treatment and decreased overall QoL (P = 0.002) and emotional QoL (P = 0.02) ; few radiotherapy late toxicity symptoms (pain and decreased physical QoL, P = 0.01 ; fibrosis and decreased emotional QoL, P = 0.04) ; probable depression or probable anxiety and decreased overall, physical and emotional QoL (P ≤ 0.005). In multivariate analyses, probable depression and probable anxiety were the most stronger predictors for decreased QoL in the overall, physical and emotional domains (P ≤ 0.02). CONCLUSION: Improving screening for and treatment of depression and anxiety might improve QoL in long-term breast cancer survivors.
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- 2012
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7. Impact de l’âge sur la mortalité des patients traumatisés médullaires hospitalisés en réanimation [Impact of age on mortality in patients with acute traumatic spinal cord injury requiring intensive care]
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Seguin, Philippe, Godard, A., Le Maguet, Pascale, Launey, Yoann, Laviolle, Bruno, Mallédant, Yannick, Foie, métabolismes et cancer, Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Service d'anesthésie réanimation chirurgicale [Rennes], Université de Rennes (UR)-Hôpital Pontchaillou, Service de pharmacologie biologique et toxicologie [Rennes], Hôpital Pontchaillou-CHU Pontchaillou [Rennes], Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Hôpital Pontchaillou-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), and Le Corre, Morgane
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Âge ,MESH: Aged, 80 and over ,MESH: Risk Factors ,MESH: Analysis of Variance ,MESH: Hospital Mortality ,MESH: Intensive Care ,MESH: Spinal Cord Injuries ,Réanimation ,MESH: Treatment Outcome ,MESH: Age Factors ,MESH: Survivors ,MESH: Aged ,MESH: Humans ,MESH: Middle Aged ,MESH: Patient Discharge ,MESH: Adult ,MESH: Retrospective Studies ,[SDV.MHEP.HEG]Life Sciences [q-bio]/Human health and pathology/Hépatology and Gastroenterology ,MESH: Recovery of Function ,[SDV.MHEP.HEG] Life Sciences [q-bio]/Human health and pathology/Hépatology and Gastroenterology ,MESH: Male ,MESH: Prospective Studies ,MESH: Independent Living ,MESH: Young Adult ,MESH: Survival Analysis ,Traumatisme médullaire ,MESH: Acute Disease ,MESH: Coronary Disease ,MESH: Female - Abstract
National audience; Objective To evaluate the impact of age (< or ≥ 65 ans) on hospital mortality in traumatic spinal cord injury requiring intensive care. Design Retrospective, monocenter. Patients and methods A total of 131 patients greater or equal to 15 years (< 65 years, n = 109 and ≥ 65 years, n = 22) was analyzed (cervical, n = 71; thoracolumbar, n = 60), over a 10 years period (1998-2008). The hospital and long-term mortality were studied. The risks factors of death were searched by a uni- and multivariate analysis. Intensive care unit (ICU) discharge and long-term neurological recovery, and long-term functional independence measure (FIM) were assessed. Results Hospital mortality was increased in patients greater or equal to 65 years (41% vs 6%, P < 0.001) and long term mortality was not different between the two groups (31% vs 12%, P = 0.150). The risks factors of death were age (HR = 3.44; IC 95%: 1.53-7.72, P = 0.028), previous coronary disease (HR = 3.64; IC 95%: 1.25-10.65; P = 0.018) and fall injury (HR = 2.40; IC 95%: 1.15-5.00, P = 0.020). Among survivors, incompletes forms (Frankel B, C, D, E) were significantly more frequent in older patients at ICU discharge and long term follow up. At long term, FIM was similar in the two groups except a better sphincter control in patient greater or equal to 65 years. Conclusion Mortality rate of older people (≥ 65 years) were greater than those in younger people, mainly caused by an increased hospital mortality. Among survivors, the neurological recovery was better in patients' greater or equal to 65 years, and was associated with a functional status at least comparable than in the youngest patients.
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- 2012
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8. Prédicteurs de qualité de vie à long terme dans le cancer du sein
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Brunault, Paul, Toledano, Alain, Aguerre, Colette, Suzanne, Isabelle, Garaud, Pascal, Trzepidur-Edom, Magdalena, Calais, Gilles, Camus, Vincent, Brunault, Paul, Clinique Psychiatrique Universitaire [Tours], Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Oncologie Radiothérapie, Clinique Hartmann - Hôpital américain de paris, Psychologie des âges de la vie et adaptation (PAVeA), Université de Tours (UT), Clinique d'Oncologie et de Radiothérapie [Tours] (CORAD), Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)-Hôpital Bretonneau, Imagerie et cerveau (iBrain - Inserm U1253 - UNIV Tours ), and Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)
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MESH: Survivors ,MESH: Humans ,MESH: Middle Aged ,MESH: Radiotherapy ,MESH: breast cancer ,MESH: Depression ,MESH: Anxiety ,[SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH: Quality of Life ,MESH: Follow-Up Studies ,humanities ,MESH: France ,MESH: long-term survivors ,MESH: Analysis of Variance ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH: Esthetics ,MESH: Female ,MESH: Breast Neoplasms ,MESH: Chemoradiotherapy - Abstract
International audience; INTRODUCTION: This study aimed to assess the impact of late treatment toxicity (especially radiotherapy toxicity), chemoradiotherapy treatment type (concurrent or sequential), depression and anxiety on overall, physical and emotional quality of life (QoL) in long-term breast cancer survivors. Method. We assessed 117 patients (mean follow-up since the end of treatment = 8.1 years) for late radiotherapy toxicity (LENT-SOMA scale), patient and doctor ratings of breast cosmetic outcomes, QoL (EORTC QLQ-C30), depression and anxiety (Hospital and Anxiety Depression scale). RESULTS: In univariate analyses, factors associated with significantly decreased QoL were: use of sequential treatment and decreased overall QoL (P = 0.002) and emotional QoL (P = 0.02) ; few radiotherapy late toxicity symptoms (pain and decreased physical QoL, P = 0.01 ; fibrosis and decreased emotional QoL, P = 0.04) ; probable depression or probable anxiety and decreased overall, physical and emotional QoL (P ≤ 0.005). In multivariate analyses, probable depression and probable anxiety were the most stronger predictors for decreased QoL in the overall, physical and emotional domains (P ≤ 0.02). CONCLUSION: Improving screening for and treatment of depression and anxiety might improve QoL in long-term breast cancer survivors.
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- 2012
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9. Barriers to procreational intentions among cancer survivors 2 years after diagnosis: a French national cross-sectional survey
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Mancini, Julien, Rey, Dominique, Préau, Marie, Le Corroller-Soriano, Anne Gaëlle, Moatti, Jean-Paul, Sciences Economiques et Sociales de la Santé & Traitement de l'Information Médicale (SESSTIM - U912 INSERM - Aix Marseille Univ - IRD), Institut de Recherche pour le Développement (IRD)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), Laboratoire d'Enseignement et de Recherche sur le Traitement de l'Information Médicale (LERTIM), Université de la Méditerranée - Aix-Marseille 2, Service de Santé Publique et d'Information Médicale (SSPIM), Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE), ORS PACA, Laboratoire de Psychologie Education, Cognition, Développement (LABéCD), Université de Nantes (UN), This survey was initiated by the ‘Direction de la recherche, des études, de l'évaluation et des statistiques' (DREES) and was additionally supported by the ‘Ligue Nationale contre le Cancer'. This work was made possible by the involvement and support of the ‘Caisse Nationale de l'Assurance Maladie des Travailleurs Salariés' (CNAMTS), the ‘Mutualité sociale agricole' (MSA), and the ‘Régime social des indépendants' (RSI)., and Mancini, Julien
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Male ,Reproductive Behavior ,Intention ,Risk Factors ,MESH: Risk Factors ,Neoplasms ,Surveys and Questionnaires ,MESH: Neoplasms ,Survivors ,MESH: Survivors ,MESH: Aged ,MESH: Middle Aged ,MESH: Sex Distribution ,MESH: European Continental Ancestry Group ,Middle Aged ,MESH: Young Adult ,oncology ,Female ,France ,Adult ,MESH: Socioeconomic Factors ,socio-economic status ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,procreational intentions ,Article ,White People ,Young Adult ,Age Distribution ,national survey ,MESH: Cross-Sectional Studies ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,Humans ,cancer ,cancer survivors ,MESH: Reproductive Behavior ,Sex Distribution ,MESH: Age Distribution ,Aged ,parenthood ,MESH: Humans ,MESH: Questionnaires ,MESH: Fertility ,MESH: Adult ,MESH: Intention ,MESH: Male ,MESH: France ,Cross-Sectional Studies ,Fertility ,Socioeconomic Factors ,[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,MESH: Female - Abstract
International audience; Objectives: To determine the procreational intention rates among cancer survivors whose fertility was unimpaired and to identify the factors associated with their procreational intentions.Methods: Six thousand nine hundred and fifty-seven adult cancer patients treated between September and October 2002 were randomly selected from the French National Health Insurance Fund's Chronic Disease File. Of the 6957, 4270 responded to a cross-sectional questionnaire 2 years after diagnosis, of whom 959 reported being fertile and responded to a question about their procreational intentions.Results: Among the 257 male and female survivors aged 20-44, 86 (33.5%) had procreational intentions. After adjusting for age, gender, and already having children, only a high educational level (adjusted odds ratio: 3.1, 95% confidence interval 1.3-7.8) and stable or increasing financial resources (2.4, 1.0-5.7) were independently associated with the respondents' procreational intentions. Neither cancer stage at diagnosis nor the present stage significantly affected their plans in this respect.Conclusions: Two years after cancer diagnosis, the reasons why some survivors who are still fertile have no parenthood projects were similar to those earlier given by members of the general population. Copyright (c) 2010 John Wiley & Sons, Ltd.
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- 2011
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10. Onset and relapse of psychiatric disorders following early breast cancer: a case-control study.: Mental health of primary breast cancer survivors
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Karen Ritchie, Patrick Boulet, Isabelle Carrière, Maryvonne Soulier, Aziz Hermès, C. Gandubert, Isabelle Chaudieu, Chantal Escot, Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM), CRLC Val d'Aurelle-Paul Lamarque, CRLCC Val d'Aurelle - Paul Lamarque, Service de psychiatrie adulte, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Service de radiologie, Fondation de France, INSERM, and Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
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MESH: Psychiatric Status Rating Scales ,Stress Disorders, Post-Traumatic ,0302 clinical medicine ,Psychiatric history ,Recurrence ,Survivors ,relapse ,MESH: Survivors ,MESH: Middle Aged ,Mental Disorders ,PTSD ,Middle Aged ,Anxiety Disorders ,MESH: Case-Control Studies ,3. Good health ,Psychiatry and Mental health ,psychiatric disorders ,MESH: Stress Disorders, Post-Traumatic ,030220 oncology & carcinogenesis ,MESH: Dysthymic Disorder ,oncology ,Major depressive disorder ,Anxiety ,Female ,medicine.symptom ,medicine.medical_specialty ,Generalized anxiety disorder ,MESH: Depressive Disorder, Major ,Experimental and Cognitive Psychology ,Breast Neoplasms ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,03 medical and health sciences ,Breast cancer ,breast cancer ,medicine ,Humans ,MESH: Mental Disorders ,Psychiatry ,Mini-international neuropsychiatric interview ,Psychiatric Status Rating Scales ,Depressive Disorder, Major ,MESH: Humans ,business.industry ,Cancer ,medicine.disease ,030227 psychiatry ,MESH: Recurrence ,Mood disorders ,Case-Control Studies ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH: Anxiety Disorders ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,Dysthymic Disorder ,business ,MESH: Female ,MESH: Breast Neoplasms - Abstract
International audience; OBJECTIVE: Our objective is to evaluate the mental status of primary early breast cancer survivors according to DSM-IV criteria, distinguishing new psychiatric diagnosis, which started after the cancer diagnosis from relapse. METHODS: A comparative study of 144 breast cancer survivors and 125 women without previous history of cancer was carried out. Neuropsychiatric symptomatology was assessed retrospectively using standardized psychiatric examinations (Mini International Neuropsychiatric Interview, Watson's Post-Traumatic Stress Disorder Inventory) over three successive periods, 'before cancer' (from childhood to 3 years before the interview), 'around the cancer event' (the last 3 years including the time of diagnosis and treatment), and 'currently' (the last 2 weeks). RESULTS: Increased rates of anxiety and mood disorders were observed following a diagnosis of breast cancer compared with controls (generalized anxiety disorder (GAD) and major depressive disorder (MDD); 10.4 vs 1.6% and 19.4 vs 8.8%, respectively). The cancer disease promoted the development of dysthymia (n=4 new cases/6 two-year prevalent cases) and PTSD (7/7) and the re-emergence of MDD (n=21 relapses/28 three-year prevalent cases) and GAD (10/15). No improvement in serious mood disorders such as MDD (16.0 vs 7.2%) and dysthymia (4.2 vs 0%) was reported at the time of interview, more than 1.75 years (median time) after the cancer surgery, the prevalence being 2-4 times greater in breast cancer survivors than in controls. CONCLUSION: Despite significant advances in treatment, a diagnosis of breast cancer is highly associated with various forms of psychopathology, regardless of psychiatric history, with symptoms persisting after treatment. These results may assist clinicians in planning mental healthcare for women with breast cancer.
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- 2009
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11. Netrin-1 acts as a survival factor for aggressive neuroblastoma
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Dwayne G. Stupack, Agnès Bernet, Akira Nakagawara, Alain Puisieux, Dominique Valteau-Couanet, Marie-Anne Raquin, Raphael Rousseau, Valérie Combaret, Patrick Mehlen, Julien Fitamant, Andrea Paradisi, Céline Delloye-Bourgeois, Sétha Douc-Rasy, Jean Bénard, David Cappellen, Apoptose Cancer et Développement, Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Interactions moléculaires et cancer (IMC (UMR 8126)), Signalisation, noyaux et innovations en cancérologie (UMR8126), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS)-Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Département de Pédiatrie, Institut Gustave Roussy (IGR), departement of Pathology, University of California [San Diego] (UC San Diego), University of California-University of California, Division od Biochemistry, Chiba Center Center Research Institute, Centre Léon Bérard [Lyon], Laboratoire d'Oncologie Moléculaire, equipe 2, Oncogénèse et progression tumorale, Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM), Département de biologie et pathologie médicales [Gustave Roussy], Apoptosis, Cancer, and Development Laboratory, Bissardon, Bérangère, and University of California (UC)-University of California (UC)
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MESH: Cell Death ,Dependence receptor ,[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology ,Metastasis ,Neuroblastoma ,0302 clinical medicine ,MESH: Reverse Transcriptase Polymerase Chain Reaction ,Netrin ,MESH: RNA, Small Interfering ,MESH: Up-Regulation ,Immunology and Allergy ,Survivors ,RNA, Small Interfering ,Receptor ,MESH: Survivors ,0303 health sciences ,Cell Death ,Reverse Transcriptase Polymerase Chain Reaction ,MESH: Infant, Newborn ,MESH: Gene Expression Regulation, Neoplastic ,MESH: Neoplasm Staging ,Netrin-1 ,Prognosis ,MESH: Infant ,Up-Regulation ,3. Good health ,Gene Expression Regulation, Neoplastic ,MESH: Cell Survival ,030220 oncology & carcinogenesis ,Programmed cell death ,animal structures ,MESH: Cell Line, Tumor ,Cell Survival ,Immunology ,Biology ,Disease-Free Survival ,Article ,MESH: Prognosis ,03 medical and health sciences ,Downregulation and upregulation ,Cell Line, Tumor ,medicine ,Humans ,MESH: Tumor Suppressor Proteins ,Nerve Growth Factors ,Autocrine signalling ,Neoplasm Staging ,030304 developmental biology ,MESH: Humans ,MESH: Nerve Growth Factors ,Tumor Suppressor Proteins ,fungi ,Infant, Newborn ,Infant ,[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology ,medicine.disease ,MESH: Neuroblastoma ,nervous system ,MESH: Disease-Free Survival ,Cancer research - Abstract
International audience; Neuroblastoma (NB), the most frequent solid tumor of early childhood, is diagnosed as a disseminated disease in >60% of cases, and several lines of evidence support the resistance to apoptosis as a prerequisite for NB progression. We show that autocrine production of netrin-1, a multifunctional laminin-related molecule, conveys a selective advantage in tumor growth and dissemination in aggressive NB, as it blocks the proapoptotic activity of the UNC5H netrin-1 dependence receptors. We show that such netrin-1 up-regulation is a potential marker for poor prognosis in stage 4S and, more generally, in NB stage 4 diagnosed infants. Moreover, we propose that interference with the netrin-1 autocrine loop in malignant neuroblasts could represent an alternative therapeutic strategy, as disruption of this loop triggers in vitro NB cell death and inhibits NB metastasis in avian and mouse models.
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- 2009
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12. Onset and relapse of psychiatric disorders following early breast cancer: a case-control study
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Gandubert, Catherine, Carrière, Isabelle, Escot, Chantal, Soulier, Maryvonne, Hermès, Aziz, Boulet, Patrick, Ritchie, Karen, Chaudieu, Isabelle, Villebrun, Dominique, Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), CRLC Val d'Aurelle-Paul Lamarque, CRLCC Val d'Aurelle - Paul Lamarque, Service de psychiatrie adulte, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Service de radiologie, and Fondation de France, INSERM
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relapse ,MESH: Survivors ,MESH: Psychiatric Status Rating Scales ,MESH: Humans ,MESH: Middle Aged ,[SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,MESH: Depressive Disorder, Major ,PTSD ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,MESH: Case-Control Studies ,MESH: Recurrence ,breast cancer ,psychiatric disorders ,MESH: Stress Disorders, Post-Traumatic ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie ,MESH: Dysthymic Disorder ,[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health ,oncology ,MESH: Mental Disorders ,MESH: Anxiety Disorders ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,MESH: Female ,MESH: Breast Neoplasms - Abstract
International audience; OBJECTIVE: Our objective is to evaluate the mental status of primary early breast cancer survivors according to DSM-IV criteria, distinguishing new psychiatric diagnosis, which started after the cancer diagnosis from relapse. METHODS: A comparative study of 144 breast cancer survivors and 125 women without previous history of cancer was carried out. Neuropsychiatric symptomatology was assessed retrospectively using standardized psychiatric examinations (Mini International Neuropsychiatric Interview, Watson's Post-Traumatic Stress Disorder Inventory) over three successive periods, 'before cancer' (from childhood to 3 years before the interview), 'around the cancer event' (the last 3 years including the time of diagnosis and treatment), and 'currently' (the last 2 weeks). RESULTS: Increased rates of anxiety and mood disorders were observed following a diagnosis of breast cancer compared with controls (generalized anxiety disorder (GAD) and major depressive disorder (MDD); 10.4 vs 1.6% and 19.4 vs 8.8%, respectively). The cancer disease promoted the development of dysthymia (n=4 new cases/6 two-year prevalent cases) and PTSD (7/7) and the re-emergence of MDD (n=21 relapses/28 three-year prevalent cases) and GAD (10/15). No improvement in serious mood disorders such as MDD (16.0 vs 7.2%) and dysthymia (4.2 vs 0%) was reported at the time of interview, more than 1.75 years (median time) after the cancer surgery, the prevalence being 2-4 times greater in breast cancer survivors than in controls. CONCLUSION: Despite significant advances in treatment, a diagnosis of breast cancer is highly associated with various forms of psychopathology, regardless of psychiatric history, with symptoms persisting after treatment. These results may assist clinicians in planning mental healthcare for women with breast cancer.
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- 2009
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13. [Radiochemotherapy for oesophageal cancer: a locoregional failure history]
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Créhange, G., Maingon, P., Bosset, Jean-François, Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC ( CEF2P / CARCINO ), Centre Hospitalier Régional Universitaire [Besançon] ( CHRU Besançon ) -Université Bourgogne Franche-Comté ( UBFC ) -Université de Franche-Comté ( UFC ), Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC (EA 3181) (CEF2P / CARCINO), Université de Franche-Comté (UFC), and Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)
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MESH: Combined Modality Therapy ,Esophageal Neoplasms ,MESH: Survival Rate ,MESH: Treatment Failure ,MESH : Survivors ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Adenocarcinoma ,[ SDV.CAN ] Life Sciences [q-bio]/Cancer ,MESH : Adenocarcinoma ,MESH : Treatment Failure ,Image Processing, Computer-Assisted ,Humans ,Survivors ,Treatment Failure ,MESH : Carcinoma, Squamous Cell ,MESH: Radiotherapy Dosage ,MESH: Survivors ,MESH: Humans ,MESH : Radiotherapy Dosage ,MESH: Adenocarcinoma ,MESH : Humans ,Radiotherapy Dosage ,MESH: Carcinoma, Squamous Cell ,MESH : Survival Rate ,Combined Modality Therapy ,MESH: Image Processing, Computer-Assisted ,Survival Rate ,MESH: Esophageal Neoplasms ,Carcinoma, Squamous Cell ,MESH : Esophageal Neoplasms ,MESH : Combined Modality Therapy ,MESH : Image Processing, Computer-Assisted - Abstract
International audience; Esophageal cancer is characterized by various degrees of lymph node invasion and metastasis, both of which are associated with a poor prognosis. Exclusive concomitant radiochemotherapy (RCT) at a dose of 50 Gy delivered over 25 sessions, according to the RTOG 85-01 protocol, has led to improved five-year survival in 25% of patients, whereas no patients survive for five years using radiotherapy alone. Surgery, even when combined with preoperative RCT, also gives disappointing results for locally advanced tumors, which casts serious doubts on the usefulness of preoperative radiotherapy. By varying the fractionation schedule, the length of treatment or the radiotherapy volumes, it has become possible to obtain levels of locoregional relapse of around 35 to 45%. The increasing incidence of adenocarcinoma, which differs from epidermoid cancer with regard to the degree of lymph node invasion, has revived discussion on radiotherapy volumes. Given this difference between these two histological forms, we propose here a number of recommendations concerning radiotherapy volumes for patients presenting with cancer of the esophagus. Finally, analysis of the results for locoregional relapse according to the dose of radiation and the recommended radiotherapy volumes, has led us to investigate why increasing the dose of radiation has no impact in esophageal cancers.
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- 2008
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14. Senescence of reproduction may explain adaptive menopause in humans: a test of the 'mother' hypothesis
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Evelyne Heyer, C. Jessica E. Metcalf, Samuel Pavard, Eco-Anthropologie et Ethnobiologie (EAE), Muséum national d'Histoire naturelle (MNHN)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Max Planck Institute for Demographic Research (MPIDR), Max-Planck-Gesellschaft, and Centre National de la Recherche Scientifique (CNRS)-Université Paris Diderot - Paris 7 (UPD7)-Muséum national d'Histoire naturelle (MNHN)
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0106 biological sciences ,Aging ,MESH: Menopause ,[SDV]Life Sciences [q-bio] ,[SHS.ANTHRO-BIO]Humanities and Social Sciences/Biological anthropology ,MESH: Reproduction ,01 natural sciences ,MESH: Child ,Adaptation, Psychological ,Medicine ,MESH: Aging ,Survivors ,Child ,Maternal Behavior ,ComputingMilieux_MISCELLANEOUS ,media_common ,MESH: Survivors ,0303 health sciences ,Reproduction ,Stillbirth ,Mother-Child Relations ,Menopause ,MESH: Stillbirth ,MESH: Survival Analysis ,Female ,Anatomy ,Senescence ,MESH: Mother-Child Relations ,media_common.quotation_subject ,Fertility ,010603 evolutionary biology ,03 medical and health sciences ,Humans ,MESH: Adaptation, Psychological ,Survival analysis ,Selection (genetic algorithm) ,030304 developmental biology ,MESH: Humans ,[SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE] ,business.industry ,medicine.disease ,Survival Analysis ,El Niño ,Anthropology ,MESH: Maternal Behavior ,Adaptation ,business ,MESH: Female ,Demography - Abstract
The "mother" hypothesis is one of the main adaptive explanations of human menopause. It postulates that reproductive cessation constitutes a strategy that has been selected for during human evolution because mothers at older ages might maximize their fitness by investing resources in the survival and reproduction of their living children rather than by continuing to reproduce. This study provides a test of this hypothesis. Fertility functions that maximize fitness are built into a model incorporating the fact that the survival of females during the rearing period is a major determinant of their children's survival. Results are given according to different scenarios of increase with mothers' age of maternal mortality risk and risk of stillbirth and birth defects (on the assumption that these females do not experience menopause). Different estimates of the effect of a mother's death on her child's survival were also incorporated. Finally, a population genetics framework allows us to estimate selection on these optimal fertility functions. To determine whether or not these fertility functions show a menopause, three criteria are discussed: the rapidity of fertility decline, if any; the magnitude of selection on menopause compared with a nonmenopausal strategy; and the selection on survival during post-reproductive life. Our results show that menopause and subsequent post-reproductive life are significantly advantageous when two conditions are satisfied: a marked increase in stillbirth and risk of birth defects as well as in maternal mortality with mother's age.
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- 2008
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15. Risk of a second malignant neoplasm after cancer in childhood treated with radiotherapy: correlation with the integral dose restricted to the irradiated fields
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Sylvie Guerin, Ibrahima Diallo, Dimitri Lefkopoulos, Michael M. Hawkins, Florent de Vathaire, Odile Oberlin, Carole Rubino, Akthar Samand, Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC ( CEF2P / CARCINO ), Centre Hospitalier Régional Universitaire [Besançon] ( CHRU Besançon ) -Université Bourgogne Franche-Comté ( UBFC ) -Université de Franche-Comté ( UFC ), Epidémiologie des cancers : Radiocarcinogénèse et effets iatrogènes des traitements, Université Paris-Sud - Paris 11 ( UP11 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Department of Public Health and Epidemiology, University of Birmingham [Birmingham], Scottish Universities Physics Alliance ( SUPA ), University of Edinburgh, Département de Pédiatrie, Institut Gustave Roussy ( IGR ), Département de radiothérapie [Gustave Roussy], Carcinogénèse épithéliale : facteurs prédictifs et pronostiques - UFC (EA 3181) (CEF2P / CARCINO), Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), Université Paris-Sud - Paris 11 (UP11)-Institut National de la Santé et de la Recherche Médicale (INSERM), Scottish Universities Physics Alliance (SUPA), and Institut Gustave Roussy (IGR)
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Oncology ,Male ,MESH: Neoplasms, Radiation-Induced ,Neoplasms, Radiation-Induced ,medicine.medical_treatment ,MESH: Regression Analysis ,[ SDV.CAN ] Life Sciences [q-bio]/Cancer ,Correlation ,0302 clinical medicine ,MESH : Child ,MESH: Child ,MESH : Regression Analysis ,MESH : Hodgkin Disease ,Medicine ,MESH: Incidence ,MESH : Neoplasms, Second Primary ,Child ,Radiation ,MESH: Risk ,Incidence ,MESH : Infant ,MESH: Bone Neoplasms ,MESH: Infant ,MESH : Incidence ,3. Good health ,MESH : Antineoplastic Agents ,Integral dose ,England ,030220 oncology & carcinogenesis ,Child, Preschool ,Cohort ,Regression Analysis ,MESH : Dose-Response Relationship, Radiation ,Cohort study ,medicine.medical_specialty ,MESH : Cohort Studies ,Antineoplastic Agents ,Bone Neoplasms ,03 medical and health sciences ,MESH : Adolescent ,Humans ,MESH : Bone Neoplasms ,MESH: Adolescent ,MESH: Humans ,MESH: Child, Preschool ,MESH : Humans ,Infant ,Dose-Response Relationship, Radiation ,medicine.disease ,MESH : Neoplasms ,Radiation therapy ,Relative risk ,MESH: Antineoplastic Agents ,MESH: Female ,Cancer Research ,MESH : Risk ,MESH : Child, Preschool ,030218 nuclear medicine & medical imaging ,Cohort Studies ,MESH: England ,Neoplasms ,MESH: Neoplasms ,MESH : Female ,Survivors ,MESH: Radiotherapy Dosage ,MESH: Cohort Studies ,MESH : Neoplasms, Radiation-Induced ,MESH: Survivors ,MESH : England ,MESH : Radiotherapy Dosage ,MESH: Infant, Newborn ,Neoplasms, Second Primary ,Radiotherapy Dosage ,Hodgkin Disease ,MESH: Hodgkin Disease ,MESH: Sarcoma, Ewing's ,MESH : Sarcoma, Ewing's ,Female ,France ,Risk ,MESH: Neoplasms, Second Primary ,Adolescent ,MESH : Survivors ,MESH : Male ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Sarcoma, Ewing ,MESH : Infant, Newborn ,Internal medicine ,MESH: Dose-Response Relationship, Radiation ,Radiology, Nuclear Medicine and imaging ,MESH : France ,Chemotherapy ,business.industry ,Infant, Newborn ,Cancer ,MESH: Male ,MESH: France ,business ,Nuclear medicine - Abstract
International audience; PURPOSE: After successful treatment of cancers in childhood, the occurrence of second malignant neoplasm (SMN) came to the fore. Few studies have considered the relationship between the radiation dose received and the risk of developing an SMN. To take into account the heterogeneity of the dose distribution so as to evaluate the overall risk of an SMN after a childhood cancer, we therefore focused on the integral dose restricted to the irradiated fields. METHODS AND MATERIALS: The study was performed in a cohort of 4,401 patients who were 3-year survivors of all types of childhood cancer treated between 1947 and 1986 in France and Great Britain. For each patient, the integral dose was estimated for the volume inside the beam edges. RESULTS: We found a significant dose-response relationship between the overall risk of an SMN and the estimated integral dose. The excess relative risk for each incremental unit of the integral dose was only 0.008 in a linear model and 0.017 when a negative exponential term was considered, when adjusted for chemotherapy. The risk of SMN occurrence was 2.6 times higher in the case of irradiation. However among patients who had received radiotherapy, only those who had received the highest integral dose actually had a higher risk. CONCLUSIONS: The integral dose in our study cannot be considered as a good predictor of later risks. However other studies with the same study design are obviously needed to evaluate the use of the integral dose as a tool for decision making concerning different radiotherapy techniques.
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- 2008
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16. Radiation dose as a risk factor for malignant melanoma following childhood cancer
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Stanislaw Garwicz, Sylvie Guerin, A. Dupuy, Harald Anderson, A Shamsaldin, Marie-Françoise Avril, Michael M. Hawkins, Eric Quiniou, Jean Chavaudra, F. de Vathaire, Odile Oberlin, Gudrun Svahn-Tapper, Torgil Möller, Epidémiologie des cancers : Radiocarcinogénèse et effets iatrogènes des traitements, Université Paris-Sud - Paris 11 (UP11)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de dermatologie [Paris], Université Paris Diderot - Paris 7 (UPD7)-Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-Assistance publique - Hôpitaux de Paris (AP-HP) (APHP), Département de radiothérapie [Gustave Roussy], Institut Gustave Roussy (IGR), Physique médicale, Institut Gustave Roussy (IGR)-Institut Gustave Roussy (IGR), Biophysique moléculaire, Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Curie, Department of Public Health and Epidemiology, University of Birmingham [Birmingham], Service de dermatologie, Département de médecine oncologique [Gustave Roussy], Département de Pédiatrie, Médecine nucléaire, Département d'imagerie médicale [Gustave Roussy], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), and Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
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Oncology ,Cancer Research ,MESH: Neoplasms, Radiation-Induced ,MESH: Radiotherapy ,Neoplasms, Radiation-Induced ,Skin Neoplasms ,medicine.medical_treatment ,Cohort Studies ,MESH: Risk Factors ,Risk Factors ,MESH: Child ,Neoplasms ,Medicine ,MESH: Neoplasms ,Survivors ,MESH: Radiotherapy Dosage ,Child ,MESH: Cohort Studies ,Melanoma ,MESH: Survivors ,MESH: Middle Aged ,MESH: Infant, Newborn ,Neoplasms, Second Primary ,Radiotherapy Dosage ,MESH: Follow-Up Studies ,Middle Aged ,MESH: Infant ,Child, Preschool ,Cohort ,Cohort study ,Adult ,medicine.medical_specialty ,MESH: Neoplasms, Second Primary ,Adolescent ,MESH: Melanoma ,Internal medicine ,Humans ,Risk factor ,MESH: Adolescent ,MESH: Humans ,Radiotherapy ,business.industry ,MESH: Skin Neoplasms ,MESH: Child, Preschool ,Case-control study ,Infant, Newborn ,Cancer ,Infant ,MESH: Adult ,Odds ratio ,medicine.disease ,Surgery ,Radiation therapy ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business ,Follow-Up Studies - Abstract
The aim of this study was to determine therapy-related risk factors for the development of melanoma after childhood cancer. Among 4401 3-year survivors of a childhood cancer in eight French and British centres and 25120 patients younger than 20 years old at first malignant neoplasm (FMN) extracted from the Nordic Cancer Registries, 16 patients developed a melanoma as a second malignant neoplasm (SMN). A cohort study of the French and British cohorts was performed. In a nested case-control study, the 16 patients who developed a melanoma as a SMN (cases) were matched with 3-5 controls in their respective cohort according to gender, age at the first cancer, the calendar year of occurrence of the first cancer and follow-up. Radiotherapy appeared to increase the risk of melanoma for local doses >15 Gy, Odds Ratio (OR)=13 (95% Confidence Interval (CI): 0.94-174). Regarding chemotherapy, we observed an increased OR for both alkylating agents and spindle inhibitors, OR=2.7 (95% CI: 0.5-14). Children treated for a gonadal tumour as a FMN were found to be at a higher risk of melanoma, OR=8.7 (95% CI: 0.9-86). The adjusted OR for the local radiation dose was 1.07 (95% CI: 1.00-1.15). In conclusion, radiotherapy may contribute to an increased risk of melanoma as a SMN, but only at very high doses of low linear energy transfer radiation. Common genetic origins between gonadal tumours and malignant melanomas are likely.
- Published
- 2003
17. Wine drinking and risks of cardiovascular complications after recent acute myocardial infarction
- Author
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Francois Paillard, François Boucher, Michel de Lorgeril, Jean-Louis Martin, Joël de Leiris, Patricia Salen, Techniques de l'Ingénierie Médicale et de la Complexité - Informatique, Mathématiques et Applications, Grenoble - UMR 5525 (TIMC-IMAG), Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-IMAG-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), Laboratoire Univers et Théories (LUTH (UMR_8102)), Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, PSL Research University (PSL)-PSL Research University (PSL)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Institut des Matériaux Jean Rouxel (IMN), Université de Nantes (UN)-Centre National de la Recherche Scientifique (CNRS), VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Diderot - Paris 7 (UPD7), Université de Nantes - UFR des Sciences et des Techniques (UN UFR ST), Université de Nantes (UN)-Université de Nantes (UN)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Ecole Polytechnique de l'Université de Nantes (EPUN), and Université de Nantes (UN)-Université de Nantes (UN)
- Subjects
Male ,Myocardial Infarction ,Alcohol ,Wine ,030204 cardiovascular system & hematology ,chemistry.chemical_compound ,0302 clinical medicine ,MESH: Risk Factors ,Recurrence ,Risk Factors ,030212 general & internal medicine ,Myocardial infarction ,Survivors ,Total energy ,MESH: Survivors ,MESH: Middle Aged ,MESH: Follow-Up Studies ,Middle Aged ,Prognosis ,3. Good health ,MESH: Myocardial Infarction ,MESH: Dietary Fats ,Cardiovascular Diseases ,Cardiology and Cardiovascular Medicine ,medicine.medical_specialty ,MESH: Ethanol ,MESH: Prognosis ,03 medical and health sciences ,Drug treatment ,Physiology (medical) ,Internal medicine ,medicine ,Humans ,Risk factor ,MESH: Humans ,Ethanol ,business.industry ,MESH: Cardiovascular Diseases ,medicine.disease ,Dietary Fats ,Confidence interval ,MESH: Wine ,MESH: Male ,Surgery ,MESH: Recurrence ,chemistry ,Ethanol intake ,business ,[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition ,Follow-Up Studies - Abstract
Background— Scientific data on the clinical impact of moderate alcohol consumption after a recent acute myocardial infarction (AMI) are limited, and the specific effect of wine ethanol has not been studied. Methods and Results— In survivors of a recent AMI, we analyzed the association between ethanol intake and the risk of recurrence. The patients were classified according to the amount of ethanol that they consumed regularly during follow-up. Major prognostic factors, including the severity of the prior AMI and drug treatment, were recorded and included in the analyses. Only patients with at least 2 reliable assessments of drinking (and dietary) habits were included (n=437). The average ethanol intake was 7.6% of the total energy intake, wherein wine ethanol represented 92% of the total. Among these patients, 104 cardiovascular complications occurred during a mean follow-up period of 4 years. In comparison with abstainers, the adjusted risk of complications was reduced by 59% (95% confidence interval: 17 to 80) in patients whose average ethanol intake was 7.7% of the total energy intake (about 2 drinks/day), and by 52% (95% confidence interval: 4 to 76) in those whose average ethanol intake was of 16% of energy (about 4 drinks/day). Conclusion— Whereas moderate wine drinking was associated with a significant reduction in the risk of complications in this homogenous population of coronary heart disease patients, further studies are required to confirm the data, define the clinical and biological profile of the patients who would most benefit from wine drinking after recent AMI, and examine whether the relations found are due to ethanol or other wine ingredients.
- Published
- 2002
18. Predictors of mortality and short-term physical and cognitive dependence in critically ill persons 75 years and older: a prospective cohort study
- Author
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Michel Ramakers, Jean-Jacques Parienti, Nicolas Terzi, Xavier Valette, Stéphanie Chevalier, Amélie Seguin, Cathy Gaillard, Pierre Charbonneau, Damien du Cheyron, Cédric Daubin, Fabrice Prevost, Service de réanimation médicale [CHU Caen], CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Université de Caen Normandie (UNICAEN), Normandie Université (NU), Cellule Promotion de la Recherche Clinique [CHU Caen] (CPRC), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Cognition, Mobilités, Temporalité (COMETE), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), ESIM - Déterminants Sociaux de la Santé et du Recours aux Soins (DS3), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire d'Immunologie [CHU Caen], and BMC, Ed.
- Subjects
Male ,Health Status ,Dependency, Psychological ,MESH: Cognition ,MESH: Comorbidity ,Comorbidity ,older persons intensive care unit ,intensive care unit ,MESH: Length of Stay ,0302 clinical medicine ,MESH: Aged, 80 and over ,Cognition ,Quality of life ,MESH: Risk Factors ,Risk Factors ,Activities of Daily Living ,Medicine ,030212 general & internal medicine ,Prospective Studies ,Survivors ,Prospective cohort study ,MESH: Health Status ,MESH: Aged ,MESH: Survivors ,Aged, 80 and over ,education.field_of_study ,General Medicine ,MESH: Follow-Up Studies ,functional autonomy ,3. Good health ,Intensive Care Units ,MESH: Critical Illness ,lcsh:R858-859.7 ,SOFA score ,Female ,Cohort study ,MESH: Forecasting ,medicine.medical_specialty ,MESH: Dependency (Psychology) ,Critical Care ,Critical Illness ,Population ,lcsh:Computer applications to medicine. Medical informatics ,03 medical and health sciences ,Internal medicine ,Intensive care ,Humans ,MESH: Intensive Care ,Intensive care medicine ,education ,Aged ,MESH: Humans ,business.industry ,Research ,MESH: Activities of Daily Living ,Public Health, Environmental and Occupational Health ,MESH: Quality of Life ,030208 emergency & critical care medicine ,Odds ratio ,Length of Stay ,mortality ,MESH: Male ,MESH: Prospective Studies ,Nottingham Health Profile ,quality of life ,[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie ,older persons ,MESH: Intensive Care Units ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business ,MESH: Female ,Follow-Up Studies ,Forecasting - Abstract
Background The purpose of this study was to identify predictors of 3-month mortality in critically ill older persons under medical care and to assess the clinical impact of an ICU stay on physical and cognitive dependence and subjective health status in survivors. Methods We conducted a prospective observational cohort study including all older persons 75 years and older consecutively admitted into ICU during a one-year period, except those admitted after cardiac arrest, All patients were followed for 3 months or until death. Comorbidities were assessed using the Charlson index and physical dependence was evaluated using the Katz index of Activity of Daily Living (ADL). Cognitive dependence was determined by a score based on the individual components of the Lawton index of Daily Living and subjective health status was evaluated using the Nottingham Health Profile (NHP) score. Results One hundred patients were included in the analysis. The mean age was 79.3 ± 3.4 years. The median Charlson index was 6 [IQR, 4 to 7] and the mean ADL and cognitive scores were 5.4 ± 1.1 and 1.2 ± 1.4, respectively, corresponding to a population with a high level of comorbidities but low physical and cognitive dependence. Mortality was 61/100 (61%) at 3 months. In multivariate analysis only comorbidities assessed by the Charlson index [Adjusted Odds Ratio, 1.6; 95% CI, 1.2-2.2; p < 0.003] and the number of organ failures assessed by the SOFA score [Adjusted Odds Ratio, 2.5; 95% CI, 1.1-5.2; p < 0.02] were independently associated with 3-month mortality. All 22 patients needing renal support after Day 3 died. Compared with pre-admission, physical (p = 0.04), and cognitive (p = 0.62) dependence in survivors had changed very little at 3 months. In addition, the mean NHP score was 213.1 ± 132.8 at 3 months, suggesting an acceptable perception of their quality of life. Conclusions In a selected population of non surgical patients 75 years and older, admission into the ICU is associated with a 3-month survival rate of 38% with little impact on physical and cognitive dependence and subjective health status. Nevertheless, a high comorbidity level (ie, Charlson index), multi-organ failure, and the need for extra-renal support at the early phase of intensive care could be considered as predictors of death.
- Published
- 2011
- Full Text
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