Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 7 de 7
Filtrer
1.
Rev. Asoc. Odontol. Argent ; 110(3): 1101201, sept.-dic. 2022.
Article de Espagnol | LILACS | ID: biblio-1419164

RÉSUMÉ

Las evaluaciones radiográficas de tratamientos endodón- ticos realizadas por graduados muestran un alto porcentaje de procedimientos incorrectos. Esta circunstancia lleva a la rea- lización de un elevado número de retratamientos ortógrados y retrógrados, con los inconvenientes y desventajas que conlle- va recurrir a una reintervención endodóntica. Es responsabili- dad de los profesionales, docentes y autoridades universitarias y gubernamentales revertir esta situación que afecta a la salud bucal de la sociedad. En el presente editorial se proponen di- ferentes alternativas para intentar modificar este preocupante panorama (AU)


Radiographic evaluations of endodontic treatments per- formed by graduates show a high percentage of incorrect procedures. This circumstance leads to the performance of a high number of orthograde and retrograde retreatments, with the inconveniences and disadvantages that entails resorting to an endodontic reintervention. It is the responsibility of pro- fessionals, teachers, university and government authorities to reverse this situation that affects the oral health of society. In this editorial, different alternatives are proposed to try to modify this worrying outlook (AU)


Sujet(s)
Traitement de canal radiculaire/méthodes , Dent dévitalisée/imagerie diagnostique , Reprise du traitement/effets indésirables , Erreurs médicales/statistiques et données numériques , Échec de restauration dentaire/statistiques et données numériques , Enseignement dentaire/méthodes , Évaluation des acquis scolaires , Endodontie/enseignement et éducation
2.
Article de Anglais, Portugais | LILACS, Sec. Est. Saúde SP | ID: biblio-1136743

RÉSUMÉ

ABSTRACT Objective: To assess clinical predictors and outcomes associated to the need for surfactant retreatment in preterm infants. Methods: Retrospective cohort study, including very low birth weight preterm infants from January 2006 to December 2015 who underwent surfactant replacement therapy. Beractant was used (100 mg/kg), repeated every six hours if FiO2 ≥0.40. The subjects were classified into two groups: single surfactant dose; and more than one dose (retreatment). We evaluated maternal and neonatal predictors for the need of retreatment and neonatal outcomes associated to retreatment. Results: A total of 605 patients (44.5%) received surfactant; 410 (67.8%) one dose, and 195 (32.2%) more than one dose: 163 (83.5%) two doses and 32 (16.4%) three doses. We could not find clinical predictors for surfactant retreatment. Retreatment was associated to a greater chance of BPD in infants >1000 g (RR 1.78; 95%CI 1.30‒2.45) and ≤1000 g (RR 1.33; 95%CI 1.04‒1.70), in infants with gestational age<28 weeks (RR 1.56; 95%CI 1.12‒2.18) and ≥28 weeks (RR 1.50; 95%CI 1.17‒1.92), in neonates with early sepsis (RR 1.48; 95%CI 1.20‒1.81), and in infants not exposed to antenatal corticosteroids (RR 1.62; 95%CI 1.20‒2.17) Conclusions: We could not find predictor factors associated to surfactant retreatment. The need for two or more doses of surfactant was significantly related to bronchopulmonary dysplasia.


RESUMO Objetivo: Avaliar preditores clínicos e resultados associados à necessidade de retratamento com surfactante. Métodos: Coorte retrospectiva com prematuros de muito baixo peso, no período de janeiro de 2006 a dezembro de 2015, em uso de terapia de reposição de surfactante. O surfactante utilizado foi beractante (100 mg/kg), repetido a cada seis horas se FiO2≥0.40. Foram analisados dois grupos: dose única de surfactante e mais de uma dose (retratamento). Foram avaliados preditores maternos e neonatais para retratamento e resultados neonatais. Resultados: 605 pacientes (44,5%) receberam surfactante; 410 (67,8%) uma dose e 195 (32,2%) mais de uma dose: 163 (83,5%) duas doses e 32 (16.4%) três doses. Não foram encontrados fatores associados ao retratamento com surfactante. A displasia broncopulmonar (DBP) foi associada ao retratamento (p<0.01). A presença de retratamento aumentou a chance de ocorrência de DBP em neonatos >1000 g (RR 1,78; IC95% 1,30‒2,45) e ≤1000 g (RR 1,33; IC95% 1,04‒1,70), em recém-nascidos com idade gestacional <28 semanas (RR 1,56; IC95% 1,12‒218) e ≥28 semanas (RR 1,50; IC95% 1,17‒1,92), naqueles com sepse precoce (RR 1,48; IC95% 1,20‒1,81), e nos que não foram expostos ao corticoide antenatal (RR 1,62; IC95% 1,20‒2,17). Conclusões: Não encontramos fatores preditores associados à necessidade de retratamento. A necessidade de duas ou mais doses de surfactante está associada à displasia broncopulmonar.


Sujet(s)
Humains , Mâle , Femelle , Enfant d'âge préscolaire , Syndrome de détresse respiratoire du nouveau-né/traitement médicamenteux , Produits biologiques/administration et posologie , Surfactants pulmonaires/administration et posologie , Syndrome de détresse respiratoire du nouveau-né/mortalité , Études rétrospectives , Facteurs de risque , Âge gestationnel , Reprise du traitement/effets indésirables , Reprise du traitement/statistiques et données numériques , Nourrisson de poids extrêmement faible à la naissance , Très grand prématuré
3.
Rev Paul Pediatr ; 39: e2019360, 2020.
Article de Anglais, Portugais | MEDLINE | ID: mdl-33206840

RÉSUMÉ

OBJECTIVE: To assess clinical predictors and outcomes associated to the need for surfactant retreatment in preterm infants. METHODS: Retrospective cohort study, including very low birth weight preterm infants from January 2006 to December 2015 who underwent surfactant replacement therapy. Beractant was used (100 mg/kg), repeated every six hours if FiO2 ≥0.40. The subjects were classified into two groups: single surfactant dose; and more than one dose (retreatment). We evaluated maternal and neonatal predictors for the need of retreatment and neonatal outcomes associated to retreatment. RESULTS: A total of 605 patients (44.5%) received surfactant; 410 (67.8%) one dose, and 195 (32.2%) more than one dose: 163 (83.5%) two doses and 32 (16.4%) three doses. We could not find clinical predictors for surfactant retreatment. Retreatment was associated to a greater chance of BPD in infants >1000 g (RR 1.78; 95%CI 1.30‒2.45) and ≤1000 g (RR 1.33; 95%CI 1.04‒1.70), in infants with gestational age<28 weeks (RR 1.56; 95%CI 1.12‒2.18) and ≥28 weeks (RR 1.50; 95%CI 1.17‒1.92), in neonates with early sepsis (RR 1.48; 95%CI 1.20‒1.81), and in infants not exposed to antenatal corticosteroids (RR 1.62; 95%CI 1.20‒2.17). CONCLUSIONS: We could not find predictor factors associated to surfactant retreatment. The need for two or more doses of surfactant was significantly related to bronchopulmonary dysplasia.


Sujet(s)
Produits biologiques/administration et posologie , Surfactants pulmonaires/administration et posologie , Syndrome de détresse respiratoire du nouveau-né/traitement médicamenteux , Femelle , Âge gestationnel , Humains , Nourrisson de poids extrêmement faible à la naissance , Très grand prématuré , Nouveau-né , Mâle , Syndrome de détresse respiratoire du nouveau-né/mortalité , Reprise du traitement/effets indésirables , Reprise du traitement/statistiques et données numériques , Études rétrospectives , Facteurs de risque
4.
J Gastrointest Cancer ; 49(4): 470-475, 2018 Dec.
Article de Anglais | MEDLINE | ID: mdl-28884286

RÉSUMÉ

PURPOSE: Our objective was to evaluate the benefit of re-exposing patients with refractory metastatic colorectal cancer (mCRC) to a combination of oxaliplatin, irinotecan and 5-fluorouracil treatment. METHODS: We retrospectively analysed patients with mCRC who received a combination of oxaliplatin, irinotecan and fluorouracil as a rechallenge regimen after progressing on the same drugs. Both FOLFOXIRI and FOLFIRINOX were used. Toxicity was evaluated for each treatment cycle, and survival analysis was performed using the Kaplan-Meier method. RESULTS: A total of 21 patients who were treated between January 2011 and December 2013 were selected for this study. Most of the patients (95.2%) had an ECOG status of 0-1. The median age at diagnosis was 52.1 years (range 36-77 years), and 14 (66.6%) patients had wild-type KRAS. Thirteen patients received FOLFIRINOX, and eight received FOLFOXIRI. Most patients had previously received at least three regimens, with 80% receiving anti-VEGF and 66% anti-EGFR antibodies. The response rate was 38%, and 24% patients had stable disease. The median time to disease progression was 4.0 months (range 1.0-9.1 months), and the median overall survival duration was 8.6 months (range 6.3-11.5 months). Most patients required dose adjustment and treatment delays. One patient experienced grade 5 neutropenic sepsis. CONCLUSIONS: Both FOLFIRINOX and FOLFOXIRI are active and potentially feasible rechallenge treatment options for heavily pretreated patients with good performance status. With dose reduction and close monitoring for toxicity, the risk of serious adverse events can be minimised.


Sujet(s)
Protocoles de polychimiothérapie antinéoplasique/usage thérapeutique , Camptothécine/analogues et dérivés , Neutropénie fébrile induite par la chimiothérapie/épidémiologie , Tumeurs colorectales/traitement médicamenteux , Résistance aux médicaments antinéoplasiques/effets des médicaments et des substances chimiques , Fluorouracil/usage thérapeutique , Leucovorine/usage thérapeutique , Composés organométalliques/usage thérapeutique , Adulte , Sujet âgé , Protocoles de polychimiothérapie antinéoplasique/pharmacologie , Camptothécine/pharmacologie , Camptothécine/usage thérapeutique , Neutropénie fébrile induite par la chimiothérapie/étiologie , Tumeurs colorectales/mortalité , Tumeurs colorectales/anatomopathologie , Évolution de la maladie , Survie sans rechute , Calendrier d'administration des médicaments , Association médicamenteuse , Femelle , Fluorouracil/pharmacologie , Humains , Irinotécan , Estimation de Kaplan-Meier , Leucovorine/pharmacologie , Mâle , Adulte d'âge moyen , Composés organométalliques/pharmacologie , Composés organiques du platine/pharmacologie , Composés organiques du platine/usage thérapeutique , Oxaliplatine , Reprise du traitement/effets indésirables , Reprise du traitement/méthodes , Études rétrospectives , Résultat thérapeutique
5.
Vox Sang ; 112(5): 453-458, 2017 Jul.
Article de Anglais | MEDLINE | ID: mdl-28516443

RÉSUMÉ

BACKGROUND AND OBJECTIVES: To estimate the risk of iron overload in very low birthweight (VLBW) infants who receive more than two red blood cell (RBC) transfusions, in comparison with those who receive two or less during their hospital stay. MATERIALS AND METHODS: Prospective open cohort study in VLBW infants with >2 (exposed) and ≤2 (non-exposed) RBC transfusions. Ferritin, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were measured at birth and after each RBC transfusion. The incidence of iron overload was determined. Risk factors were analysed using a logistic regression model. RBC transfusion volume correlations with ferritin, ALT and AST were calculated with Spearman's rank correlation coefficient, as well as correlations between ferritin and aminotransferases. RESULTS: A total of 63 patients were enrolled, 18 of which were exposed and 45 non-exposed. Twelve patients developed severe iron overload, eight exposed (44·5%) vs. four (8·8%) non-exposed (RR: 5, 95% CI: 1·7-14·6). Multivariate analysis showed that the number of transfusions increased the risk of iron overload (OR: 2·07, 95% CI: 1·36-2·14) while a higher one-minute Apgar score was associated with a lower risk (OR: 0·56, 95% CI: 0·32-0·99). Severe iron overload mainly occurred with a transfusion volume higher than 120 ml/kg. There was a positive correlation between ferritin and transfusion (r = 0·53; P < 0·001). CONCLUSION: There was a higher risk of iron overload in exposed infants in comparison with non-exposed infants. Severe iron overload in VLBW infants may occur with a total transfusion volume >120 ml/kg.


Sujet(s)
Anémie néonatale/thérapie , Transfusion d'érythrocytes/effets indésirables , Surcharge en fer/étiologie , Anémie néonatale/sang , Femelle , Ferritines/sang , Humains , Nouveau-né , Prématuré , Nourrisson très faible poids naissance , Mâle , Études prospectives , Reprise du traitement/effets indésirables , Facteurs de risque , Résultat thérapeutique
6.
Rev. Assoc. Paul. Cir. Dent ; 70(1): 45-48, jan.-mar. 2016. ilus
Article de Portugais | LILACS, BBO - Ondontologie | ID: lil-797052

RÉSUMÉ

Dens in dente (dens invaginatus) é uma anomalia de desenvolvimento que afeta a formados dentes. O órgão do esmalte é desorganizado e ocorre a invaginação da coroa do dente antes da fase de calcificação. O relato deste caso tem como objetivo apresentar o uso de inserto sultrassônicos e medicação intracanal com iodofórmio no retratamento endodôntico em dens indente tipo II com lesão periapical. O dente necessitou de retratamento endodôntico. O acesso coronário e a instrumentação dos canais radiculares foram realizados com auxílio de insetos ultrassônicos. Utilizou-se iodofórmio e hidróxido de cálcio como medicação intracanal em duas sessões. Na última sessão, a obturação foi realizada. Após dois anos de follow-up, observou-se sucesso no retratamento. O dente apresenta-se sem sintomatologia dolorosa e com redução da lesão periapical.


Dens in dente (dens invaginatus) is a developmental anomaly that affects the shape ofteeth. The enamel organ is disorganized and invagination of the tooth crown occurs before thecalcification stage. The aim of this case report is present the use of ultrasonic tips and intracanalmedication with iodoform in endodontic retreatment in dens in dente type II with periapicallesion. The tooth required endodontic retreatment. Coronal access and root canal instrumentationwere performed with the aid of ultrasonic tips. Iodoform and calcium hydroxide were usedas intracanal medication in two sessions. In the last session, filling was performed. After follow--up of 2 years, successful retreatment was observed. The tooth presented no painful symptomsand the periapical lesion was reduced.


Sujet(s)
Humains , Mâle , Femelle , Dens in dente , Hydroxyde de calcium/effets indésirables , Iodoformium/analyse , Parodontite périapicale/complications , Parodontite périapicale/diagnostic , Reprise du traitement/effets indésirables
7.
Int J Tuberc Lung Dis ; 6(12): 1110-3, 2002 Dec.
Article de Anglais | MEDLINE | ID: mdl-12546120

RÉSUMÉ

SETTING: BCG revaccination is not used worldwide. In Brazil, it has been recommended since 1994 in children aged 6 to 14 years. Reports in the medical literature of adverse reactions due to revaccination are rare. BCG revaccination remains officially recommended by the Brazilian health authorities, based on the current epidemiological tuberculosis situation in the country. OBJECTIVE: We report 13 cases of children and adolescents with complications due to BCG revaccination. DESIGN: Case reports of patients followed up in a pneumology unit of a university pediatric hospital from May 1996 to December 2000. RESULTS: There were seven males and six females, whose ages ranged from 7-12 years. Adverse reactions occurred between 21 days and 9 months after BCG revaccination. All 13 cases had a scar from prior BCG vaccination. All cases treated received isoniazid, 10 mg/kg/day, in the morning until the end of cure. The duration of treatment varied, but all cases were successfully cured. CONCLUSION: Although adverse reactions are rare, it is important to continue monitoring them in order to learn more about them and to be able to orient health professionals to perform appropriate assessment and timely treatment when they occur.


Sujet(s)
Abcès/induit chimiquement , Vaccin BCG/effets indésirables , Reprise du traitement/effets indésirables , Maladies de la peau/induit chimiquement , Ulcère cutané/induit chimiquement , Tuberculose/prévention et contrôle , Adolescent , Facteurs âges , Brésil , Enfant , Femelle , Humains , Mâle
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE