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1.
J Evid Based Dent Pract ; 23(3): 101863, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37689449

RESUMEN

BACKGROUND: Dual antiplatelet therapy (DAPT) provides additional risk reduction of ischemic events compared to aspirin monotherapy, at cost of higher bleeding risk. There are few data comparing new techniques for reducing bleeding after dental extractions in these patients. PURPOSE: This study investigated the effectiveness of the HemCon Dental Dressing (HDD) compared to oxidized cellulose gauze. MATERIALS AND METHODS: This randomized study included 60 patients on DAPT who required at least two dental extractions (120 procedures). Each surgical site was randomized to HDD or oxidized regenerated cellulose gauze as the local hemostatic method. Intra-oral bleeding time was measured immediately after the dental extraction and represents our main endpoint for comparison of both hemostatic agents. Prolonged bleeding, platelet reactivity measured by Multiplate Analyser (ADPtest and ASPItest) and tissue healing comparison after 7 days were also investigated. RESULTS: Intra-oral bleeding time was lower in HDD compared with control (2 [2-5] vs. 5 [2-8] minutes, P=0.001). Prolonged postoperative bleeding was observed in 7 cases (11.6%), all of them successfully managed with local sterile gauze pressure. More HDD treated sites presented better healing when compared with control sites [21 (36.8%) vs. 5 (8.8%), P=0.03]. There was poor correlation between platelet reactivity and intra-oral bleeding time. CONCLUSIONS: In patients on DAPT, HDD resulted in a lower intra-oral bleeding time compared to oxidized cellulose gauze after dental extractions. Moreover, HDD also seems to improve healing conditions.


Asunto(s)
Celulosa Oxidada , Hemostáticos , Humanos , Celulosa Oxidada/uso terapéutico , Inhibidores de Agregación Plaquetaria/uso terapéutico , Persona Soltera , Método Simple Ciego , Hemostáticos/uso terapéutico , Extracción Dental
2.
Clin Transplant ; 33(8): e13658, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31271675

RESUMEN

BACKGROUND: Cardiovascular mortality is increased in chronic kidney disease, a condition with a high prevalence of periodontal disease. Whether periodontitis treatment improves prognosis is unknown. METHODS: The effect of periodontal treatment on the incidence of cardiovascular events and death in 206 waitlist hemodialysis subjects was compared with that in 203 historical controls who did not undergo treatment. Patients were followed up for 24 months or until death or transplantation. RESULTS: The prevalence of moderate/severe periodontitis was 74%. Coronary artery disease correlated with the severity of periodontal disease (P = .02). Survival free of cardiovascular events (94% vs 83%, log-rank 0.009), coronary events (97% vs 89%, log-rank = 0.009), and cardiovascular death (96% vs 87%, log-rank = 0.037) was higher in the evaluated group. Death by any cause did not differ between groups. Multivariate analysis showed that treatment was associated with reduction in cardiovascular events (HR 0.43; 95% CI 0.22-0.87), coronary events (HR 0.31; 95% CI 0.12-0.83), and cardiovascular deaths (HR 0.43; 95% CI 0.19-0.98). CONCLUSION: Periodontal treatment reduced the 24-month incidence of cardiovascular events and cardiovascular death, suggesting that periodontal treatment may improve cardiovascular outcomes. We suggest that periodontal screening and eventual treatment may be considered in patients with advanced renal disease.


Asunto(s)
Enfermedades Cardiovasculares/prevención & control , Atención Odontológica/estadística & datos numéricos , Fallo Renal Crónico/fisiopatología , Trasplante de Riñón/mortalidad , Enfermedades Periodontales/terapia , Listas de Espera/mortalidad , Brasil/epidemiología , Enfermedades Cardiovasculares/epidemiología , Estudios de Casos y Controles , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Enfermedades Periodontales/complicaciones , Pronóstico , Estudios Retrospectivos , Factores de Riesgo
5.
Artículo en Inglés | MEDLINE | ID: mdl-37925270

RESUMEN

OBJECTIVE: Sirolimus (SRL) and everolimus (EVL) are increasingly included in immunosuppressive protocols after heart transplantation. They present some side effects, including the appearance of painful lesions in the oral cavity. Therefore, this systematic review aimed to verify the global prevalence and clinical characteristics of oral lesions induced by SRL and EVL in heart transplant patients. STUDY DESIGN: A systematic review was performed using 5 main electronic databases (Medline/PubMed, SCOPUS, EMBASE, Web of Science, and LILACS), in addition to the gray literature. Studies were independently assessed by 2 reviewers based on established eligibility criteria. The risk of bias was assessed using the Joanna Briggs Institute appraisal tools, and the certainty of evidence was evaluated through GRADE assessment. RESULTS: Seventeen studies (860 patients) were included in the qualitative analysis. Of these, 11 studies were pooled in a meta-analysis of prevalence. The worldwide prevalence of oral lesions induced by SRL and EVL in heart transplant patients was 10.0%, and most lesions were described as ulcers >1.0 cm, related to significant pain. CONCLUSIONS: Oral lesions induced by SRL and/or EVL, although not very prevalent, have a relevant impact on patient's lives and the continuity of treatment.


Asunto(s)
Everolimus , Trasplante de Corazón , Humanos , Everolimus/efectos adversos , Sirolimus/efectos adversos , Prevalencia , Inmunosupresores/efectos adversos , Trasplante de Corazón/efectos adversos
6.
Artículo en Inglés | MEDLINE | ID: mdl-34400124

RESUMEN

OBJECTIVE: Infective endocarditis (IE) may cause devastating complications with high morbidity and mortality rates. The aim of the present study was to study the demographic, cardiological, microbiologic, and dental profiles of patients with oral bacteria-related IE. STUDY DESIGN: We present a retrospective study of patients with oral bacteria-related IE treated at Instituto do Coração, Hospital das Clínicas, Faculdade de Medicina, Universidade de Sao Paulo, Brazil, between January 2009 and December 2019. RESULTS: Of the 100 patients included, 70% were male with a mean age of 45.4 years at diagnosis. The most affected sites were aortic and mitral valves, 60% in prosthetic heart valves, 34% in native valves, and 3% in pacemakers. The most common cause of valvular disease was rheumatic cardiopathy (51.9%), and the most frequent complications were valvular and perivalvular damage (26%). Streptococcus viridans was the most common species (96%), dental caries were present in 57% of the patients, 78% had tooth loss, 45% had apical periodontitis, and 77% were at high/moderate risk for periodontal disease. CONCLUSION: Oral bacteria-related IE among Brazilians was predominant in the prosthetic heart valves of young male adults previously affected by rheumatic cardiopathy. Streptococcus viridans was the main cause of IE, which was linked to patients with a poor oral health status.


Asunto(s)
Caries Dental , Endocarditis Bacteriana , Endocarditis , Adulto , Bacterias , Brasil/epidemiología , Demografía , Endocarditis/epidemiología , Endocarditis Bacteriana/epidemiología , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
7.
J Am Heart Assoc ; 8(15): e012361, 2019 08 06.
Artículo en Inglés | MEDLINE | ID: mdl-31319747

RESUMEN

Background Brugada syndrome and long-QT syndrome may account for at least one third of unexplained sudden cardiac deaths. Dental care in patients with cardiac channelopathies is challenging because of the potential risk of life-threatening events. We hypothesized that the use of local dental anesthesia with lidocaine with and without epinephrine is safe and does not result in life-threatening arrhythmias in patients with channelopathies. Methods and Results We performed a randomized, double-blind pilot trial comparing the use of 2% lidocaine without a vasoconstrictor and with 1:100 000 epinephrine in 2 sessions of restorative dental treatment with a washout period of 7 days (crossover trial). Twenty-eight-hour Holter monitoring was performed, and 12-lead electrocardiography, digital sphygmomanometry, and anxiety scale assessments were also conducted at 3 time points. Fifty-six dental procedures were performed in 28 patients (18 women, 10 men) with cardiac channelopathies: 16 (57.1%) had long-QT syndrome, and 12 (42.9%) had Brugada syndrome; 11 (39.3%) of patients had an implantable defibrillator. The mean age was 45.9±15.9 years. The maximum heart rate increased after the use of epinephrine during the anesthesia period from 82.1 to 85.8 beats per minute (P=0.008). In patients with long-QT syndrome, the median corrected QT was higher, from 450.1 to 465.4 ms (P=0.009) at the end of anesthesia in patients in whom epinephrine was used. The other measurements showed no statistically significant differences. No life-threatening arrhythmias occurred during dental treatment. Conclusions The use of local dental anesthesia with lidocaine, regardless of the use of a vasoconstrictor, did not result in life-threatening arrhythmias and appears to be safe in stable patients with cardiac channelopathies. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT03182777.


Asunto(s)
Anestésicos Locales/administración & dosificación , Síndrome de Brugada/fisiopatología , Canalopatías/fisiopatología , Contraindicaciones de los Procedimientos , Atención Odontológica/efectos adversos , Epinefrina/administración & dosificación , Lidocaína/administración & dosificación , Síndrome de QT Prolongado/fisiopatología , Vasoconstrictores/administración & dosificación , Adolescente , Adulto , Anciano , Anestésicos Locales/efectos adversos , Método Doble Ciego , Epinefrina/efectos adversos , Femenino , Humanos , Lidocaína/efectos adversos , Masculino , Persona de Mediana Edad , Proyectos Piloto , Estudios Prospectivos , Vasoconstrictores/efectos adversos
8.
Int. j. cardiovasc. sci. (Impr.) ; 36: e20200312, 2023. tab, graf
Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1430488

RESUMEN

Abstract Background Dental anesthetic management in implantable cardioverter defibrillator (ICD) recipients with cardiac channelopathies (CCh) can be challenging due to the potential risk of life-threatening arrhythmias and appropriate ICD therapies during procedural time. Objectives The present study assessed the hypothesis that the use of local dental anesthesia with 2% lidocaine with 1:100,000 epinephrine or without a vasoconstrictor can be safe in selected ICD and CCh patients, not resulting in life-threatening events (LTE). Methods Restorative dental treatment under local dental anesthesia was made in two sessions, with a wash-out period of 7 days (cross-over trial), conducting with a 28h - Holter monitoring, and 12-lead electrocardiography, digital sphygmomanometry, and anxiety scale assessments in 3 time periods. Statistical analysis carried out the paired Student's t test and the Wilcoxon signed-rank test. In all cases, a significance level of 5% was adopted. All patients were in stable condition with no recent events before dental care. Results Twenty-four consecutive procedures were performed in 12 patients (9 women, 3 men) with CCh and ICD: 7 (58.3%) had long QT syndrome (LQTS), 4 (33.3%) Brugada syndrome (BrS), and 1 (8.3%) Catecholaminergic polymorphic ventricular tachycardia (CPVT). Holter analysis showed no increased heart rate (HR) or sustained arrhythmias. Blood pressure (BP), electrocardiographic changes and anxiety measurement showed no statistically significant differences. No LTE occurred during dental treatment, regardless of the type of anesthesia. Conclusion Lidocaine administration, with or without epinephrine, can be safely used in selected CCh-ICD patients without LTE. These preliminary findings need to be confirmed in a larger population with ICD and CCh.

9.
Clinics (Sao Paulo) ; 70(3): 185-9, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26017649

RESUMEN

OBJECTIVE: To investigate the variations in blood glucose levels, hemodynamic effects and patient anxiety scores during tooth extraction in patients with type 2 diabetes mellitus T2DM and coronary disease under local anesthesia with 2% lidocaine with or without epinephrine. STUDY DESIGN: This is a prospective randomized study of 70 patients with T2DM with coronary disease who underwent oral surgery. The study was double blind with respect to the glycemia measurements. Blood glucose levels were continuously monitored for 24 hours using the MiniMed Continuous Glucose Monitoring System. Patients were randomized into two groups: 35 patients received 5.4 mL of 2% lidocaine, and 35 patients received 5.4 mL of 2% lidocaine with 1:100,000 epinephrine. Hemodynamic parameters (blood pressure and heart rate) and anxiety levels were also evaluated. RESULTS: There was no difference in blood glucose levels between the groups at each time point evaluated. Surprisingly, both groups demonstrated a significant decrease in blood glucose levels over time. The groups showed no significant differences in hemodynamic and anxiety status parameters. CONCLUSION: The administration of 5.4 mL of 2% lidocaine with epinephrine neither caused hyperglycemia nor had any significant impact on hemodynamic or anxiety parameters. However, lower blood glucose levels were observed. This is the first report using continuous blood glucose monitoring to show the benefits and lack of side effects of local anesthesia with epinephrine in patients with type 2 diabetes mellitus and coronary disease.


Asunto(s)
Anestesia Local/métodos , Enfermedad Coronaria/fisiopatología , Diabetes Mellitus Tipo 2/fisiopatología , Epinefrina/administración & dosificación , Extracción Dental/métodos , Vasoconstrictores/administración & dosificación , Adulto , Anciano , Anciano de 80 o más Años , Anestésicos Locales , Ansiedad/fisiopatología , Glucemia/análisis , Presión Sanguínea/efectos de los fármacos , Combinación de Medicamentos , Métodos Epidemiológicos , Femenino , Índice Glucémico/efectos de los fármacos , Frecuencia Cardíaca/efectos de los fármacos , Hemodinámica/efectos de los fármacos , Humanos , Lidocaína , Masculino , Persona de Mediana Edad , Factores de Tiempo , Resultado del Tratamiento
10.
Clinics (Sao Paulo) ; 69(5): 314-8, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24838895

RESUMEN

OBJECTIVES: In this observational study, we evaluated the peripheral oxygen saturation (SpO2), heart rate, and blood pressure of children with cyanotic congenital heart disease who were undergoing dental extraction. METHODS: Forty-four patients between the ages of 6 and 12 years who underwent upper primary tooth extraction were included in the study. Of these, 20 patients were in the cyanotic congenital heart disease group and 24 were in the control group. RESULTS: Peripheral oxygen saturation, heart rate, and systolic blood pressure in the cyanotic congenital heart disease group varied quite significantly during the treatment protocol (p<0.05), with values of 80.5% (±7.6) to 82.8% (±7.8), 95.3 beats per minute (bpm) (±11.3) to 101.3 bpm (±9.8), and 93.6 mm Hg (±13,3) to 103.8 mm Hg (±12.7), respectively. The variations in the control group during the procedure were also significant. CONCLUSIONS: The changes observed during the study protocol, although statistically significant, were mild and lacked clinical relevance. The results indicate that dental treatment of children with cyanotic heart disease using a standardized protocol in decentralized offices without the support of a surgical center is safe.


Asunto(s)
Presión Sanguínea/fisiología , Cardiopatías Congénitas/fisiopatología , Frecuencia Cardíaca/fisiología , Oxígeno/sangre , Anestésicos Locales/uso terapéutico , Presión Sanguínea/efectos de los fármacos , Niño , Cianosis/fisiopatología , Ansiedad al Tratamiento Odontológico/psicología , Frecuencia Cardíaca/efectos de los fármacos , Humanos , Lidocaína/uso terapéutico , Oximetría , Extracción Dental
11.
Arq Bras Cardiol ; 98(5): 452-8, 2012 May.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-22522720

RESUMEN

BACKGROUND: Benzathine penicillin G every 3 weeks is the standard protocol for secondary prophylaxis for recurrent rheumatic fever. OBJECTIVE: Assess the effect of Benzathine penicillin G on Streptococcus sanguinis and Streptococcus oralis in patients with cardiac valvular disease due to rheumatic fever receiving secondary prophylaxis. METHODS: Oral streptococci were evaluated before (baseline) and after 7 days (day 7) with Benzathine penicillin G in 100 patients receiving routine secondary rheumatic fever prophylaxis. Saliva samples were evaluated for colony count and presence of S. sanguinis and S. oralis. Chewing-stimulated saliva samples were serially diluted and plated onto both nonselective and selective 5% sheep blood agar containing penicillin G. The species were identified using conventional biochemical tests. Minimal inhibitory concentrations were determined with the Etest. RESULTS: No statistical differences were found in the presence of S. sanguinis comparing baseline and day 7 (p = 0.62). However, the existing number of positive cultures of S. oralis on day 7 after Benzathine penicillin G presented a significant increase compared to baseline (p = 0.04). No statistical difference was found between baseline and day 7 concerning the number of S. sanguinis or S. oralis CFU/mL and median minimal inhibitory concentrations. CONCLUSION: This study showed that Benzathine penicillin G every 3 weeks did not change the colonization by S. sanguinis, but increased colonization of S. oralis on day 7 of administration. Therefore, susceptibility of Streptococcus sanguinis and Streptococcus oralis to penicillin G was not modified during the penicillin G routine secondary rheumatic fever prophylaxis.


Asunto(s)
Antibacterianos/administración & dosificación , Boca/microbiología , Penicilina G/administración & dosificación , Resistencia a las Penicilinas/efectos de los fármacos , Estreptococos Viridans/efectos de los fármacos , Adolescente , Adulto , Niño , Esquema de Medicación , Femenino , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Fiebre Reumática/prevención & control , Estadísticas no Paramétricas , Factores de Tiempo , Adulto Joven
12.
Clinics ; 70(3): 185-189, 03/2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-747109

RESUMEN

OBJECTIVE: To investigate the variations in blood glucose levels, hemodynamic effects and patient anxiety scores during tooth extraction in patients with type 2 diabetes mellitus T2DM and coronary disease under local anesthesia with 2% lidocaine with or without epinephrine. STUDY DESIGN: This is a prospective randomized study of 70 patients with T2DM with coronary disease who underwent oral surgery. The study was double blind with respect to the glycemia measurements. Blood glucose levels were continuously monitored for 24 hours using the MiniMed Continuous Glucose Monitoring System. Patients were randomized into two groups: 35 patients received 5.4 mL of 2% lidocaine, and 35 patients received 5.4 mL of 2% lidocaine with 1:100,000 epinephrine. Hemodynamic parameters (blood pressure and heart rate) and anxiety levels were also evaluated. RESULTS: There was no difference in blood glucose levels between the groups at each time point evaluated. Surprisingly, both groups demonstrated a significant decrease in blood glucose levels over time. The groups showed no significant differences in hemodynamic and anxiety status parameters. CONCLUSION: The administration of 5.4 mL of 2% lidocaine with epinephrine neither caused hyperglycemia nor had any significant impact on hemodynamic or anxiety parameters. However, lower blood glucose levels were observed. This is the first report using continuous blood glucose monitoring to show the benefits and lack of side effects of local anesthesia with epinephrine in patients with type 2 diabetes mellitus and coronary disease. .


Asunto(s)
Adulto , Humanos , Masculino , Citocinas/sangre , Infecciones por VIH/sangre , Linfoma Relacionado con SIDA/sangre , Linfoma de Células B/sangre , Linfoma de Células B/virología , Biomarcadores de Tumor/sangre , Bisexualidad , Estudios de Casos y Controles , Infecciones por VIH/inmunología , Homosexualidad , Inflamación/sangre , Inflamación/inmunología , Inflamación/virología , Activación de Linfocitos , Linfoma Relacionado con SIDA/inmunología , Linfoma de Células B/inmunología , Análisis Multivariante
13.
Clinics (Sao Paulo) ; 64(3): 177-82, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19330241

RESUMEN

OBJECTIVES: This study analyzes hemodynamic changes in patients with cardiac valvular diseases submitted to dental treatment under local anesthesia containing epinephrine. METHODS: This randomized clinical trial was performed at the Dental Division of the Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (Brazil). Patients were separated into two groups with the help of an aleatory number table: 2% plain lidocaine (PL, n= 31) and 2% lidocaine with epinephrine (1:100,000) (LE, n= 28). Blood pressure, heart rate, oxygenation and electrocardiogram data were all recorded throughout the procedure. State and trait anxiety levels were measured. RESULTS: Fifty-nine patients were selected for the LE group (n=28), with an average age of 40.3 +/- 10.9, or for the PL group (n=31), age 42.2 +/- 10.3. No differences were shown in blood pressure, heart rate and pulse oximetry values before, during and after local anesthesia injection between the two groups. State and trait anxiety levels were not different. Arrhythmias observed before dental anesthesia did not change in shape or magnitude after treatment. Complaints of pain during the dental procedure were more frequent within the PL group, which received a higher amount of local anesthesia. CONCLUSION: Lidocaine with epinephrine (1:100,000) provided effective local anesthesia. This treatment did not cause an increase in heart rate or blood pressure and did not cause any arrhythmic changes in patients with cardiac valvular diseases.


Asunto(s)
Anestesia Dental/métodos , Anestésicos Locales/administración & dosificación , Epinefrina/administración & dosificación , Enfermedades de las Válvulas Cardíacas , Lidocaína/administración & dosificación , Vasoconstrictores/administración & dosificación , Adolescente , Adulto , Anciano , Anestesia Dental/efectos adversos , Anestésicos Locales/efectos adversos , Presión Sanguínea/efectos de los fármacos , Atención Dental para Enfermos Crónicos/métodos , Electrocardiografía/efectos de los fármacos , Epinefrina/efectos adversos , Frecuencia Cardíaca/efectos de los fármacos , Humanos , Lidocaína/efectos adversos , Persona de Mediana Edad , Oxígeno/sangre , Vasoconstrictores/efectos adversos , Adulto Joven
14.
Clinics ; 69(5): 314-318, 2014. tab
Artículo en Inglés | LILACS | ID: lil-709615

RESUMEN

OBJECTIVES: In this observational study, we evaluated the peripheral oxygen saturation (SpO2), heart rate, and blood pressure of children with cyanotic congenital heart disease who were undergoing dental extraction. METHODS: Forty-four patients between the ages of 6 and 12 years who underwent upper primary tooth extraction were included in the study. Of these, 20 patients were in the cyanotic congenital heart disease group and 24 were in the control group. RESULTS: Peripheral oxygen saturation, heart rate, and systolic blood pressure in the cyanotic congenital heart disease group varied quite significantly during the treatment protocol (p<0.05), with values of 80.5% (±7.6) to 82.8% (±7.8), 95.3 beats per minute (bpm) (±11.3) to 101.3 bpm (±9.8), and 93.6 mm Hg (±13,3) to 103.8 mm Hg (±12.7), respectively. The variations in the control group during the procedure were also significant. CONCLUSIONS: The changes observed during the study protocol, although statistically significant, were mild and lacked clinical relevance. The results indicate that dental treatment of children with cyanotic heart disease using a standardized protocol in decentralized offices without the support of a surgical center is safe. .


Asunto(s)
Niño , Humanos , Presión Sanguínea/fisiología , Cardiopatías Congénitas/fisiopatología , Frecuencia Cardíaca/fisiología , Oxígeno/sangre , Anestésicos Locales/uso terapéutico , Presión Sanguínea/efectos de los fármacos , Cianosis/fisiopatología , Ansiedad al Tratamiento Odontológico/psicología , Frecuencia Cardíaca/efectos de los fármacos , Lidocaína/uso terapéutico , Oximetría , Extracción Dental
15.
Arq Bras Cardiol ; 93(5): 463-742, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20084307

RESUMEN

BACKGROUND: The effects of local dental anesthesia with lidocaine and epinephrine on cardiovascular parameters of pregnant women with heart valve diseases and their fetuses are not fully understood. OBJECTIVES: To assess and analyze cardiotocographic, blood pressure and electrocardiographic parameters of pregnant women with rheumatic heart valve disease undergoing local anesthesia with 1.8mL of lidocaine 2% with or without epinephrine 1:100,000 during restorative dental treatment. METHODS: Maternal ambulatory blood pressure and electrocardiographic monitoring as well as cardiotocography of 31 patients with rheumatic heart disease were performed between the 28th and 37th week of gestation. The patients were divided into two groups, those with or without vasoconstrictor. RESULTS: A significant reduction in maternal heart rate was shown in both groups during the procedure in comparison with the other periods (p<0.001). Cardiac arrhythmia was observed in nine (29.0%) patients, of which seven (41.8%) were from the group of 17 pregnant women who received anesthesia plus epinephrine. No difference in maternal blood pressure was observed when periods or groups were compared (p>0.05). The same occurred (p>0.05) with the number of uterine contractions, baseline level and variability, and number of accelerations of fetal heart rate. CONCLUSION: The use of 1.8mL of lidocaine 2% in combination with epinephrine was safe and efficient in restorative dental procedures during pregnancy in women with rheumatic heart valve disease.


Asunto(s)
Anestesia Dental/efectos adversos , Anestésicos Locales/efectos adversos , Epinefrina/efectos adversos , Lidocaína/efectos adversos , Complicaciones del Embarazo/fisiopatología , Cardiopatía Reumática/fisiopatología , Adolescente , Adulto , Análisis de Varianza , Anestésicos Combinados/administración & dosificación , Anestésicos Combinados/efectos adversos , Anestésicos Locales/administración & dosificación , Arritmias Cardíacas/inducido químicamente , Presión Sanguínea/efectos de los fármacos , Cardiotocografía , Epinefrina/administración & dosificación , Femenino , Edad Gestacional , Frecuencia Cardíaca Fetal/efectos de los fármacos , Humanos , Lidocaína/administración & dosificación , Monitoreo Ambulatorio/métodos , Embarazo , Estadísticas no Paramétricas , Vasoconstrictores/administración & dosificación , Vasoconstrictores/efectos adversos , Adulto Joven
16.
Arq Bras Cardiol ; 91(3): 128-33, 142-7, 2008 Sep.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-18853053

RESUMEN

BACKGROUND: The routine use of local anesthetics associated to vasoconstrictors for the dental treatment of patients with cardiopathies is still controversial, due to the risk of adverse cardiovascular effects. OBJECTIVE: To evaluate and compare the hemodynamic effects of the use of local anesthetics with a non-adrenergic vasoconstrictor in patients with ventricular arrhythmia, when compared to the use of anesthetics without vasoconstrictor. METHODS: A prospective randomized study evaluated 33 patients with positive serology for Chagas' disease and 32 patients with coronary artery disease that presented complex ventricular arrhythmia at Holter monitoring (>10 EV/h and NSVT), of which 21 were females, aged 54.73 + 7.94 years, submitted to routine dental treatment with pterygomandibular anesthesia. These patients were divided in two groups: group I received prilocaine 3% associated with felypressin 0.03 IU/ml and group II received lidocaine 2% without vasoconstrictor. The number and complexity of extrasystoles were analyzed, as well as the heart rate and systemic arterial pressure of the patients on the day before, one hour before, during the procedure and one hour after the dental procedure. RESULTS: No hemodynamic alterations or increase in the number and complexity of the ventricular arrhythmia related to the anesthetic used in the dental procedure were observed in either group. CONCLUSION: The results suggest that prilocaine 3% associated to a felypressin 0.03 IU/ml can be safely used in patients with Chagas' disease or coronariopathy with complex ventricular arrhythmia.


Asunto(s)
Anestesia Dental/efectos adversos , Anestésicos Locales/efectos adversos , Arritmias Cardíacas/fisiopatología , Cardiomiopatía Chagásica/fisiopatología , Vasoconstrictores/efectos adversos , Adolescente , Adulto , Anciano , Presión Sanguínea/efectos de los fármacos , Electrocardiografía Ambulatoria , Felipresina/efectos adversos , Femenino , Frecuencia Cardíaca/efectos de los fármacos , Humanos , Lidocaína/efectos adversos , Masculino , Persona de Mediana Edad , Prilocaína/efectos adversos , Estudios Prospectivos , Factores de Tiempo , Adulto Joven
17.
Arq Bras Cardiol ; 88(5): 545-51, 2007 May.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-17589629

RESUMEN

BACKGROUND: The use of vasoconstrictors for local anesthesia in patients with coronary heart disease is controversial in the literature, and there is concern regarding risk of cardiac decompensation. OBJECTIVE: To evaluate electrocardiographic and blood pressure parameters during restorative dental procedure under local anesthesia with and without a vasoconstrictor in patients with coronary artery disease. METHODS: Sixty-two patients were included in the study, ages ranging from 39 to 80 (mean 58.7 +/- 8.8), 51 (83.2%) of whom were male. Thirty patients were randomly assigned to receive 2% lidocaine with epinephrine (epinephrine group), and the remaining patients, 2% lidocaine without epinephrine (non-epinephrine group) for local anesthesia. All patients underwent 24-hour ambulatory blood pressure monitoring and dynamic electrocardiography. Three periods were considered in the study: 1) baseline--recordings obtained during the 60 minutes prior to the procedure; 2) procedure--recordings obtained from the beginning of anesthesia to the end of the procedure and 3) 24 hours. RESULTS: There was an increase in blood pressure in both groups during the procedure, compared with baseline values; but when the two groups were compared no significant difference was detected between them. Heart rate remained unchanged in both groups. No ST-segment depression > 1 mm occurred either at baseline or during the procedure. Seven patients (12.5%) experienced more than ten arrhythmia episodes per hour during the procedure, four (13.8%) in the non-epinephrine group and three (11.1%) in the epinephrine group. CONCLUSION: No difference was observed in blood pressure, heart rate, or evidence of ischemia and arrhythmias in either group. The use of vasoconstrictor has proved to be safe within the range of the present study.


Asunto(s)
Anestesia Dental/métodos , Anestésicos Locales/administración & dosificación , Enfermedad de la Arteria Coronaria , Atención Dental para Enfermos Crónicos/métodos , Epinefrina/administración & dosificación , Lidocaína/administración & dosificación , Vasoconstrictores/administración & dosificación , Adulto , Anciano , Anciano de 80 o más Años , Anestesia Dental/efectos adversos , Anestésicos Locales/efectos adversos , Presión Sanguínea/efectos de los fármacos , Electrocardiografía , Epinefrina/efectos adversos , Femenino , Humanos , Lidocaína/efectos adversos , Masculino , Persona de Mediana Edad , Vasoconstrictores/efectos adversos
18.
Arq. bras. cardiol ; 98(5): 452-458, maio 2012. graf, tab
Artículo en Portugués | LILACS | ID: lil-643648

RESUMEN

FUNDAMENTO: Penicilina G benzatina a cada 3 semanas é o protocolo padrão para a profilaxia secundária para febre reumática recorrente. OBJETIVO: Avaliar o efeito da penicilina G benzatina em Streptococcus sanguinis e Streptococcus oralis em pacientes com doença valvular cardíaca, devido à febre reumática com recebimento de profilaxia secundária. MÉTODOS: Estreptococos orais foram avaliados antes (momento basal) e após 7 dias (7º dia) iniciando-se com penicilina G benzatina em 100 pacientes que receberam profilaxia secundária da febre reumática. Amostras de saliva foram avaliadas para verificar a contagem de colônias e presença de S. sanguinis e S. oralis. Amostras de saliva estimulada pela mastigação foram serialmente diluídas e semeadas em placas sobre agar-sangue de ovelhas seletivo e não seletivo a 5% contendo penicilina G. A identificação da espécie foi realizada com testes bioquímicos convencionais. Concentrações inibitórias mínimas foram determinadas com o Etest. RESULTADOS: Não foram encontradas diferenças estatísticas da presença de S. sanguinis comparando-se o momento basal e o 7º dia (p = 0,62). No entanto, o número existente de culturas positivas de S. oralis no 7º dia após a Penicilina G benzatina apresentou um aumento significativo em relação ao valor basal (p = 0,04). Não houve diferença estatística existente entre o momento basal e o 7º dia sobre o número de S. sanguinis ou S. oralis UFC/mL e concentrações inibitórias medianas. CONCLUSÃO: O presente estudo mostrou que a Penicilina G benzatina a cada 3 semanas não alterou a colonização por S. sanguinis, mas aumentou a colonização de S. oralis no 7º dia de administração. Portanto, a susceptibilidade do Streptococcus sanguinis e Streptococcus oralis à penicilina G não foi modificada durante a rotina de profilaxia secundária da febre reumática utilizando a penicilina G. (Arq Bras Cardiol. 2012; [online].ahead print, PP.0-0).


BACKGROUND: Benzathine penicillin G every 3 weeks is the standard protocol for secondary prophylaxis for recurrent rheumatic fever. OBJECTIVE: Assess the effect of Benzathine penicillin G on Streptococcus sanguinis and Streptococcus oralis in patients with cardiac valvular disease due to rheumatic fever receiving secondary prophylaxis. METHODS: Oral streptococci were evaluated before (baseline) and after 7 days (day 7) with Benzathine penicillin G in 100 patients receiving routine secondary rheumatic fever prophylaxis. Saliva samples were evaluated for colony count and presence of S. sanguinis and S. oralis. Chewing-stimulated saliva samples were serially diluted and plated onto both nonselective and selective 5% sheep blood agar containing penicillin G. The species were identified using conventional biochemical tests. Minimal inhibitory concentrations were determined with the Etest. RESULTS: No statistical differences were found in the presence of S. sanguinis comparing baseline and day 7 (p = 0.62). However, the existing number of positive cultures of S. oralis on day 7 after Benzathine penicillin G presented a significant increase compared to baseline (p = 0.04). No statistical difference was found between baseline and day 7 concerning the number of S. sanguinis or S. oralis CFU/mL and median minimal inhibitory concentrations. CONCLUSION: This study showed that Benzathine penicillin G every 3 weeks did not change the colonization by S. sanguinis, but increased colonization of S. oralis on day 7 of administration. Therefore, susceptibility of Streptococcus sanguinis and Streptococcus oralis to penicillin G was not modified during the penicillin G routine secondary rheumatic fever prophylaxis. (Arq Bras Cardiol. 2012; [online].ahead print, PP.0-0).


Asunto(s)
Adolescente , Adulto , Niño , Femenino , Humanos , Persona de Mediana Edad , Adulto Joven , Antibacterianos/administración & dosificación , Boca/microbiología , Penicilina G/administración & dosificación , Resistencia a las Penicilinas/efectos de los fármacos , Estreptococos Viridans/efectos de los fármacos , Esquema de Medicación , Modelos Logísticos , Fiebre Reumática/prevención & control , Estadísticas no Paramétricas , Factores de Tiempo
19.
Clinics ; 64(3): 177-182, 2009. graf, tab
Artículo en Inglés | LILACS | ID: lil-509436

RESUMEN

OBJECTIVES: This study analyzes hemodynamic changes in patients with cardiac valvular diseases submitted to dental treatment under local anesthesia containing epinephrine. METHODS: This randomized clinical trial was performed at the Dental Division of the Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (Brazil). Patients were separated into two groups with the help of an aleatory number table: 2 percent plain lidocaine (PL, n= 31) and 2 percent lidocaine with epinephrine (1:100,000) (LE, n= 28). Blood pressure, heart rate, oxygenation and electrocardiogram data were all recorded throughout the procedure. State and trait anxiety levels were measured. RESULTS: Fifty-nine patients were selected for the LE group (n=28), with an average age of 40.3 ± 10.9, or for the PL group (n=31), age 42.2 ± 10.3. No differences were shown in blood pressure, heart rate and pulse oximetry values before, during and after local anesthesia injection between the two groups. State and trait anxiety levels were not different. Arrhythmias observed before dental anesthesia did not change in shape or magnitude after treatment. Complaints of pain during the dental procedure were more frequent within the PL group, which received a higher amount of local anesthesia. CONCLUSION: Lidocaine with epinephrine (1:100,000) provided effective local anesthesia. This treatment did not cause an increase in heart rate or blood pressure and did not cause any arrhythmic changes in patients with cardiac valvular diseases.


Asunto(s)
Adolescente , Adulto , Anciano , Humanos , Persona de Mediana Edad , Adulto Joven , Anestesia Dental/métodos , Anestésicos Locales/administración & dosificación , Epinefrina/administración & dosificación , Enfermedades de las Válvulas Cardíacas , Lidocaína/administración & dosificación , Vasoconstrictores/administración & dosificación , Anestesia Dental/efectos adversos , Anestésicos Locales/efectos adversos , Presión Sanguínea/efectos de los fármacos , Atención Dental para Enfermos Crónicos/métodos , Electrocardiografía/efectos de los fármacos , Epinefrina/efectos adversos , Frecuencia Cardíaca/efectos de los fármacos , Lidocaína/efectos adversos , Oxígeno/sangre , Vasoconstrictores/efectos adversos , Adulto Joven
20.
Rev. Soc. Cardiol. Estado de Säo Paulo ; 19(2,supl.A): 18-22, abr.-jun. 2009. ilus
Artículo en Portugués | LILACS | ID: lil-526820

RESUMEN

Um caso clínico de sindrome da maquiagem de kabuki é apresentado. Trata-se de síndrome rara, com prevalência entre 1:32.000 e 50.000 nascimentos. As implicações odontológicas estão principalmente associadas ao risco de endocardite infecciosa, uma vez que mais de 40 por cento dos pacientes apresentam alterações cardíacas congênitas. A presença de déficit cognitivo requer atenção especial, pois interfere na manutenção da saúde bucal. O conhecimento clínico dessa condição e de suas manifestações sistêmicas é importante para que conduta odontológica correta seja instituída.


Asunto(s)
Humanos , Preescolar , Cardiopatías Congénitas/complicaciones , Personal de Odontología en Hospital , Salud Bucal
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