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1.
Arch Pediatr ; 22(5): 468-75, 2015 May.
Artículo en Francés | MEDLINE | ID: mdl-25725972

RESUMEN

AIM: To assess knowledge acquired by adolescents about their inflammatory bowel disease (IBD). METHODS: An anonymous questionnaire was given during consultation to adolescents followed for IBD by pediatricians from 13 hospitals between 1 September 2012 and 1 July 2013. After parental consent, these physicians completed a form at the inclusion of each patient, in which the characteristics of IBD were detailed. The patients mailed back their questionnaire. RESULTS: A total of 124 patients from 12 to 19 years of age were included with a response rate of 82% (all anonymous); 23% of the patients thought that diet was a possible cause of IBD and 22% that one of the targets of their treatment was to cure their disease for good. Of the patients reported having Crohn disease, 46% knew the anoperineal location and 14% knew that Crohn disease can affect the entire digestive tract. Twenty-five percent of the patients were able to name one side effect of azathioprine (88% had already received this treatment), 24% were able to name one side effect of infliximab (54% had already received this treatment), 70% of the adolescents knew that smoking worsens Crohn disease, 68% declared they had learned about their IBD from their pediatrician, and 81% said they would like to receive more information. CONCLUSION: Adolescents with IBD have gaps in their general knowledge and the different treatments of their disease. Their main source of information is their pediatrician, warranting the implementation of customized patient education sessions.


Asunto(s)
Colitis Ulcerosa/psicología , Enfermedad de Crohn/psicología , Alfabetización en Salud , Adolescente , Azatioprina/efectos adversos , Azatioprina/uso terapéutico , Colitis Ulcerosa/tratamiento farmacológico , Colitis Ulcerosa/etiología , Enfermedad de Crohn/tratamiento farmacológico , Enfermedad de Crohn/etiología , Estudios Transversales , Conducta Alimentaria , Femenino , Francia , Humanos , Infliximab/efectos adversos , Infliximab/uso terapéutico , Masculino , Educación del Paciente como Asunto , Factores de Riesgo , Fumar/efectos adversos , Fumar/psicología , Encuestas y Cuestionarios
2.
Arch Pediatr ; 11(5): 412-6, 2004 May.
Artículo en Francés | MEDLINE | ID: mdl-15135422

RESUMEN

UNLABELLED: Studies concerning very preterm newborns are either defined by birth weight (<1500 g) or gestational age (<32 weeks). The aim of our study was to underline limits of cohort definitions by birth weight. METHODS: Data come from the Nord Pas de Calais EPIPAGE cohort. Every birth occurring in 1997 before 32 weeks or with a birth weight less than 1500 g and transferred in a neonatal unit was included. Two cohorts were defined, one by gestational age (<32 weeks), the other by birth weight (<1500 g). Two subgroups could be defined from these to cohorts: group A (<32 weeks and > or =1500 g), from cohort (<32 weeks), group B (> or =32 weeks and <1500 g) from cohort (<1500 g). RESULTS: Five hundred nine newborns were included. Perinatal characteristics of both cohorts seemed comparable. The analysis by subgroups A and B revealed an excess of pulmonary and neurological morbidity in very preterm infant compared to very low birth weight newborn. This was linked to an excess of growth restricted newborns in this cohort with more advanced gestational ages. CONCLUSION: Cohorts of very preterm newborns should rather be defined by gestational age. If not possible, results in very low birth weight cohorts should also be given by gestational age and rate of growth restriction should be described.


Asunto(s)
Retardo del Crecimiento Fetal , Recien Nacido Prematuro , Recién Nacido de muy Bajo Peso , Desarrollo Infantil , Estudios de Cohortes , Femenino , Edad Gestacional , Humanos , Recién Nacido , Enfermedades Pulmonares/etiología , Enfermedades Pulmonares/patología , Masculino , Morbilidad , Enfermedades del Sistema Nervioso/etiología , Enfermedades del Sistema Nervioso/patología , Valores de Referencia
3.
J Heart Valve Dis ; 10(5): 675-80, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11603608

RESUMEN

BACKGROUND AND AIM OF THE STUDY: Aortic valve replacement (AVR) for mechanical prosthetic valvular testing has not been performed in calves because of anatomic difficulties, and sheep have traditionally been used in this situation. Hemodynamically, however, the calf constitutes an excellent model due to vigorous myocardial contractility, high stroke volumes and high cardiac output, and so has been used for preclinical evaluation of mechanical assist devices and mechanical valves in the mitral and tricuspid positions, which can be approached with relative surgical ease. Recently, a juvenile bovine model has been used to test a newly developed mechanical valve in the aortic position. METHODS: Ten calves (body weight 91+/-11 kg) underwent AVR with a 21-mm mechanical prosthesis via a small left intercostal thoracotomy with the aid of a Heartport cannulation device. A standard cardiopulmonary bypass (CPB) circuit was used. To circumvent the short bovine ascending aorta and to gain additional space to perform the aortotomy, two aortic cannulas were inserted for arterial-systemic perfusion. Nine calves each received a 21-mm experimental trileaflet aortic central flow valve prosthesis, and one calf received a 21-mm St. Jude Medical prosthesis. RESULTS: Mean CPB duration was 154.2+/-44.4 min, and mean ischemic time 80.1+/-15.9 min. Mean study duration was 42.6+/-53.7 days. Three calves were killed prematurely: two on days 2 and 7 due to complications arising from inadvertent entrapment of the right coronary artery ostium by a suture, and one on day 0 due to an accidental overdose of magnesium. Three calves, all of which had a first-version test valve, were killed electively due to valve malfunction secondary to early valvular thrombosis. Four animals (three with the final version valve and one with a standard valve as a control) survived until killed electively (range: 33-172 days). CONCLUSION: Results indicate that replacement of the native bovine aortic valve with a mechanical prosthesis can be performed safely in calves. Complication-free survival of up to six months can be achieved in the growing calf, provided that the test valve design satisfies minimum hemodynamic and coagulation criteria.


Asunto(s)
Válvula Aórtica/cirugía , Enfermedades de las Válvulas Cardíacas/terapia , Implantación de Prótesis de Válvulas Cardíacas , Animales , Peso Corporal , Cateterismo Cardíaco , Puente Cardiopulmonar , Bovinos , Enfermedades de las Válvulas Cardíacas/complicaciones , Implantación de Prótesis de Válvulas Cardíacas/instrumentación , Procedimientos Quirúrgicos Mínimamente Invasivos/instrumentación , Modelos Cardiovasculares , Complicaciones Posoperatorias/etiología , Complicaciones Posoperatorias/mortalidad , Diseño de Prótesis , Factores de Tiempo , Resultado del Tratamiento
4.
Tex Heart Inst J ; 27(3): 236-9, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11093405

RESUMEN

Microemboli caused by mechanical heart valves have the potential to cause cerebrovascular events. We investigated the effects of myocardial contractility and heart rate on microemboli production in association with conventional and experimental mechanical heart valves implanted in the mitral position in a bovine model. In 10 calves, the mitral valves were replaced with mechanical valves. Doppler recordings were analyzed for high-intensity transient signals, which are ultrasound reflections from circulating microemboli. The animals were studied at rest, during pacing at 160 bpm, after dobutamine infusion, and after esmolol infusion. The incidence of high intensity transient signals was expressed as signal frequency (signals per hour) and as signal rate (signals per 100 heart cycles). With a 68% increase in the heart rate, signal frequency increased by 135%, but signal rate increased by only 41 %. With a 144% increase in myocardial contractility, signal rate increased by 264 %. With a 31 % decrease in contractility, signal rate decreased by 62 %. We conclude that microemboli production by mechanical heart valves varies with myocardial contractility and heart rate. The fact that contractility affects the incidence of high-intensity transient signals suggests that the microemboli are gaseous in nature, that their production is pressure driven, and that cavitation is a possible cause. It is likely that mechanical heart valve design is responsible for the quantity of microemboli production.


Asunto(s)
Embolia/fisiopatología , Prótesis Valvulares Cardíacas/efectos adversos , Contracción Miocárdica , Agonistas Adrenérgicos beta/farmacología , Antagonistas Adrenérgicos beta/farmacología , Animales , Estimulación Cardíaca Artificial , Cardiotónicos/farmacología , Bovinos , Dobutamina/farmacología , Embolia/diagnóstico por imagen , Embolia/etiología , Frecuencia Cardíaca , Válvula Mitral/cirugía , Contracción Miocárdica/efectos de los fármacos , Propanolaminas/farmacología , Ultrasonografía Doppler
5.
ASAIO J ; 46(3): 344-50, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10826749

RESUMEN

In patients with mechanical heart valves (MHVs), transcranial Doppler methods commonly detect high intensity transient signals (HITS) representing microemboli. These microemboli, which are presumably gaseous, may cause stroke and cognitive deterioration. A bovine model was therefore developed for studying the relationship between mitral MHV induced HITS and potential etiogenic factors. We placed an 18 mm, 4 MHz Doppler probe in the brachiocephalic artery to detect MHV induced microbubbles at baseline (rest) and under 9 other conditions. To elucidate the gas composition (CO2 or N2) of the microbubbles, we administered 1%, 3%, and 5% CO2, and 100% O2. To determine effect of the heart rate, we paced the heart at 120, 160, and 180 bpm. To alter the myocardial contractility, we gave dobutamine and esmolol. Two independent, blinded observers counted the HITS from recorded doppler spectra. HITS were defined by an initial unidirectional spectral deviation, a signal power of >8 dB relative to the background power, and lack of a cyclic appearance. The electrocardiogram, aortic and LV pressures, and LV dP/dt were obtained telemetrically. The calves were studied 4 to 6, 8 to 10, and 12 to 14 weeks postoperatively, after which the animals were sacrificed at an approximate 4 month study duration, and a postmortem evaluation of the heart and the main viscera was performed. In all, 27 HITS recordings were made in 10 calves. Myocardial contractility was the only factor to significantly affect HITS frequency; the heart rate and blood gas concentrations had minimal effect on HITS frequency. Our bovine model will be useful for assessing valve designs, as well as the mechanism of HITS, the composition of the microemboli, and their possible pathophysiologic effects on the kidneys and brain.


Asunto(s)
Prótesis Valvulares Cardíacas/efectos adversos , Embolia Intracraneal/diagnóstico por imagen , Ultrasonografía Doppler Transcraneal/métodos , Glándulas Suprarrenales/irrigación sanguínea , Animales , Análisis de los Gases de la Sangre , Bovinos , Circulación Cerebrovascular/fisiología , Modelos Animales de Enfermedad , Frecuencia Cardíaca , Enfermedades de las Válvulas Cardíacas/complicaciones , Enfermedades de las Válvulas Cardíacas/cirugía , Embolia Intracraneal/etiología , Riñón/irrigación sanguínea , Contracción Miocárdica , Circulación Renal/fisiología , Ultrasonografía Doppler Transcraneal/instrumentación
7.
ASAIO J ; 40(3): M707-13, 1994.
Artículo en Inglés | MEDLINE | ID: mdl-8555606

RESUMEN

Design goals for a mechanical heart valve include duplicating the hemodynamic performance of the natural valve, eliminating the need for anticoagulants, and maintaining safety. The Lapeyre-Dassault (Dassault-Aviation, Paris, France) prosthetic valve, undergoing development, addresses these goals. The unique trileaflet design consists of a solid titanium ring and three leaflets. Prototypes of the valve fabricated with Delrin leaflets were implanted in the mitral position in six calves (70-90 kg). Four calves (Studies 1, 2, 3, 5) had long-term survival of 165, 158, 219, and 281 days, respectively. Two calves were killed, one on Day 37 and one on Day 39, after complications unrelated to the valve developed. In all calves heparin was given intravenously to maintain partial thromboplastin time at 1.5 to 2.0 x baseline for approximately 1 week. In Studies 1 and 2 full anticoagulation and antiplatelet therapy was given (orally administered sodium warfarin to maintain prothrombin time at 1.5 to 2.0 x baseline, along with aspirin (1 g/day) and dipyridamole 400 mg/day). In Study 3, all anticoagulation and antiplatelet therapy was discontinued at 1 month after implant. In Study 5, no anticoagulation therapy was given after the initial week of intravenous heparin; however, antiplatelet therapy was started on the fifth postoperative month and maintained until the study's end at 9 months. At 1, 2, 3, and 5 months, the mean plasma free hemoglobin level in the four long-term animals was 5.0 +/- 2.16, 6.0 +/- 3.83, 8.5 +/- 4.93, and 11.3 +/- 6.74 mg/dl, respectively. Hemolysis was not a problem. Valve performance during normal activity was excellent in all the calves, as evidenced by echocardiography and the overall appearance of good health. In the four completed long-term studies, left heart catheterization showed a mean valve pressure gradient of 11.57 +/- 1.26 mmHg and no apparent valvular regurgitation. Histopathologic examination of major organs showed no evidence of thromboembolic events. This study shows that the innovative design of this trileaflet valve performed well in initial in vivo testing, justifying further development.


Asunto(s)
Prótesis Valvulares Cardíacas , Animales , Anticoagulantes/administración & dosificación , Bovinos , Estudios de Evaluación como Asunto , Prótesis Valvulares Cardíacas/efectos adversos , Hemodinámica , Válvula Mitral/patología , Válvula Mitral/cirugía , Presión , Diseño de Prótesis , Trombosis/etiología , Trombosis/prevención & control
9.
C R Seances Soc Biol Fil ; 175(5): 559-89, 1981.
Artículo en Francés | MEDLINE | ID: mdl-6456789

RESUMEN

Reproducing the function of the natural heart with an artificial heart requires a multi-disciplinary approach. Problems to be solved are anatomical, physiological, biological and technical ones. Moreover, clinical use of the artificial heart on a large scale in the near future may involve economical, ethical and legal issues. These several aspects are reviewed, and the State of the Art in 1981 is established.


Asunto(s)
Corazón Artificial , Corazón/fisiología , Animales , Materiales Biocompatibles , Gasto Cardíaco , Perros , Corazón Artificial/economía , Hemodinámica , Humanos
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