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1.
Pacing Clin Electrophysiol ; 38(6): 723-30, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25682988

ABSTRACT

BACKGROUND: A wide variability in the perioperative management of oral anticoagulation (OAC) has been documented in patients receiving cardiac rhythm management devices (CRMDs). We sought to evaluate the safety and feasibility of a new perioperative strategy consisting in systematically continuing OAC in all patients irrespective of their individual thromboembolic (TE) risk. METHODS: A total of 278 consecutive patients on chronic OAC receiving CRMDs were prospectively included. Patients were classified in high and low TE risk according to current guidelines for the perioperative management of antithrombotic therapy, but underwent implantation under active OAC (international normalized ratio 2-4) irrespective of their preoperative TE risk. Bleeding and TE complications were evaluated as well as other procedure-related complications, hospital stays, and the feasibility of outpatient implantations. RESULTS: A total of 117 patients were considered at high TE risk and 161 at low TE risk. Overall, the incidence of pocket hematoma was 2.9% with only three patients requiring pocket revision. Low TE risk patients had a very low incidence of pocket hematoma (1.9%) without needing pocket revision. The mean hospital stay was 1.17 ± 1.8 days and 169 patients (61%) received their CRMD in an outpatient basis, including 77 patients who were implanted with an implantable cardioverter defibrillator. No TE events were detected during the 30-day postimplant observation period in any patient. No other significant complications related with the implant (pneumothorax, hemothorax, cardiac tamponade) were registered. CONCLUSIONS: Systematic continuation of OAC in all patients undergoing implantation of CRMDs is safe and feasible, thus simplifying and standardizing the perioperative management in this setting.


Subject(s)
Anticoagulants/administration & dosage , Defibrillators, Implantable , Pacemaker, Artificial , Administration, Oral , Aged , Anticoagulants/adverse effects , Defibrillators, Implantable/adverse effects , Female , Humans , International Normalized Ratio , Male , Pacemaker, Artificial/adverse effects , Prospective Studies , Treatment Outcome
2.
Metab Brain Dis ; 28(1): 107-10, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23154926

ABSTRACT

The syndrome of dyskinesia associated with hyperglycemia and basal ganglia hyperintensity on T1 - weighted MR images is rare and most often affects elderly patients with type 2 diabetes. We report a case of a 79 year-old female patient who presented to the ED with a 12 h history of a left sided hemichoreoathetosis. Laboratory results revealed pronounced nonketotic hyperglycemia [27 mmol/L (486 mg/dL); HbA1c 140 mmol/mol (15 %)] and brain MRI showed bilateral T1 hyperintensity in the basal ganglia, more noticeable on the right side. One week before she had been admitted with a diagnosis of transient ischemic attack consisting in left hemiparesthesia, also with nonketotic hyperglycemia [38.9 mmol/L (700 mg/dL)] and was discharged home with partial correction of her metabolic disturbance. The movement disorder did not improve with adequate glycemic control so haloperidol was started. Six weeks later she was seen on an outpatient basis. She still had minimal residual involuntary movements of the left arm and leg. Laboratory exams revealed a well controlled diabetes mellitus [glycemia 6.0 mmol/L (109 mg/dL), HbA1c 57 mmol/mol (7.4 %)]. In conclusion, the syndrome of dyskinesia associated to hyperglycemia and hyperintensity in the basal ganglia on T1 - weighted MR images is a rare, intriguing and yet incompletely understood complication of diabetes mellitus. The increasing number of reported cases may help to better understand its peculiarities such as the existence of a clear clinical radiological dissociation and to unveil pathophysiological aspects. We suggest the possibility that the metabolic disturbances unmask a previous established asymptomatic striatum vasculopathy.


Subject(s)
Basal Ganglia/physiopathology , Diabetes Mellitus, Type 2/complications , Dyskinesias/etiology , Hyperglycemia/complications , Aged , Chorea/etiology , Female , Humans
3.
Heart Rhythm ; 9(3): 361-7, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22001709

ABSTRACT

BACKGROUND: Perioperative management of oral anticoagulation (OAC) in patients receiving pacemakers or implantable cardioverter-defibrillators remains an issue of concern. OBJECTIVE: We sought to evaluate the safety and the effect on the hospital length of stay of a new standardized protocol for perioperative management of OAC in this setting. METHODS: The new standardized protocol classified patients according to a renewed evaluation of their thromboembolic (TE) risk. Briefly, patients were considered at moderate-to-high TE risk if they had a mechanical valvular prostheses irrespective of type and location or atrial fibrillation associated with a CHADS(2)score of ≥2, mitral stenosis or previous stroke, and underwent device implantation without stopping OAC (OAC continued, n = 129). Complete interruption of OAC before surgery was performed in low-TE-risk patients (OAC interrupted, n = 82). A retrospective cohort of patients managed with a classic heparin-bridging strategy served as a control group, with 62 patients considered at moderate-to-high TE risk according to previous guidelines (receiving pre- and postoperative low-molecular-weight heparin) and 146 considered at low TE risk (receiving only low doses of postoperative low-molecular-weight heparin). RESULTS: TE events were comparable between the 2 strategies. Patients entering the new standardized protocol had significantly lower rates of pocket hematoma (2.3% for OAC continued vs 17.7% for moderate-to-high TE risk bridging controls, P = .0001, and 0% for OAC interrupted vs 13% for low-TE-risk bridging controls, P <.0001) and shorter hospital stays. A mean of 3.34 hospitalization days per patient were saved with the new standardized protocol, with an estimated cost savings of €850.83 per patient. CONCLUSIONS: Implantation of the new standardized protocol resulted in a significant reduction in bleeding complications and hospital stays, with adequate protection against TE events and significant cost savings.


Subject(s)
Anticoagulants , Cardiac Pacing, Artificial , Perioperative Care , Postoperative Hemorrhage , Thromboembolism , Administration, Oral , Aged , Aged, 80 and over , Anticoagulants/administration & dosage , Anticoagulants/adverse effects , Cardiac Pacing, Artificial/economics , Cardiac Pacing, Artificial/methods , Cardiac Pacing, Artificial/standards , Clinical Protocols/standards , Cost Savings , Defibrillators, Implantable , Drug Substitution/methods , Drug Substitution/standards , Female , Heparin, Low-Molecular-Weight/administration & dosage , Humans , International Normalized Ratio , Length of Stay , Male , Middle Aged , Monitoring, Physiologic/methods , Multivariate Analysis , Pacemaker, Artificial , Patient Selection , Perioperative Care/methods , Perioperative Care/standards , Perioperative Care/statistics & numerical data , Postoperative Hemorrhage/epidemiology , Postoperative Hemorrhage/etiology , Postoperative Hemorrhage/prevention & control , Risk Factors , Thromboembolism/epidemiology , Thromboembolism/etiology , Thromboembolism/prevention & control
4.
Pacing Clin Electrophysiol ; 34(10): 1217-24, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21671955

ABSTRACT

BACKGROUND: Active-fixation pacing leads are being widely employed due to their theoretical advantages when compared with traditional passive-fixation leads: easy fixation and reposition, possible deployment in alternative pacing sites, lower rates of dislodgment, and chronic removability. However, the behavior of the active-fixation mechanism during lead removal has not been yet systematically studied and may have important clinical implications. OBJECTIVE: To evaluate if the active-fixation mechanism was still working properly in pacing leads that were removed due to different causes. METHODS: Thirty-one consecutive patients undergoing active-fixation lead removal (40 leads) were studied. Before lead removal, the helix was retracted using the appropriate tool, and fluoroscopy signs were evaluated. After removal, the helix status was examined, and the active-fixation mechanism was once again retested when possible. RESULTS: In nine of 40 leads (22.5%), the helix remained extended after lead removal in spite of having applied the number of rotations recommended by the manufacturer with the clip-on tool. There was no linear relationship between lead longevity and the presence of an extended helix after lead removal. However, failure of the active-fixation mechanism was more frequent among leads implanted <1 year before versus >1 year before (OR 6.8, 95% CI 1.1-42.7, P = 0.043). In 38% of patients with failure of the active-fixation mechanism, a previous lead reposition had been attempted before lead removal due to significant pacing threshold rise. CONCLUSIONS: In our series, the active-fixation mechanism failed in up to 22.5% of explanted leads. This may have important clinical implications during active-fixation lead removal and reposition.


Subject(s)
Device Removal , Electrodes, Implanted , Equipment Failure , Surgical Fixation Devices , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged
5.
Europace ; 13(3): 395-401, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21131650

ABSTRACT

AIMS: Perioperative management of antiplatelet (AP) therapy in patients undergoing implantation of cardiac rhythm management devices (CRMD) remains an issue of concern that has not been prospectively evaluated in a large series. We sought to describe the morbidity associated with three different AP regimens in this setting. METHODS AND RESULTS: We conducted a prospective observational study including 849 consecutive patients who were classified in three groups according to the presence of any AP treatment: Group 1 (n= 220): single AP therapy; Group 2 (n= 60): dual AP therapy; and Group 3 (n= 40): oral anticoagulant (OAC) + enoxaparin 'bridging' + AP therapy. Two other groups served as controls: Group 4 (n= 375): no AP or OAC therapy; and Group 5 (n= 154): OAC + enoxaparin 'bridging'. The incidence of pocket haematoma, pocket revisions, hospital stays duration, and unscheduled follow-up visits due to pocket-related complications were compared. Patients on Groups 2, 3 and 5 had significantly higher incidences of pocket haematoma (13.3, 15, and 14.9%, respectively) when compared with Groups 1 and 4 (3.2 and 2.4%, respectively), as well as longer hospital stays and more unscheduled follow-up visits. Of note, only patients on enoxaparin 'bridging' required surgical revision of the pocket. Dual AP therapy (P< 0.001), enoxaparin 'bridging' (P< 0.001) and renal insufficiency (P= 0.02) were independent predictors of pocket haematoma in multivariate analysis. CONCLUSION: Dual AP therapy and OAC + AP therapy is strongly associated with a significant risk of pocket haematoma, longer hospital stays, and unscheduled follow-up visits. Importantly, surgical revision of the pocket was associated with enoxaparin 'bridging' strategy but was never necessary in patients taking exclusively antiaggregant agents.


Subject(s)
Anticoagulants/therapeutic use , Arrhythmias, Cardiac/therapy , Cardiac Resynchronization Therapy Devices/adverse effects , Defibrillators, Implantable/adverse effects , Hematoma/prevention & control , Pacemaker, Artificial/adverse effects , Platelet Aggregation Inhibitors/therapeutic use , Aged , Aged, 80 and over , Aspirin/therapeutic use , Drug Therapy, Combination , Enoxaparin/therapeutic use , Female , Hematoma/epidemiology , Humans , Length of Stay , Male , Middle Aged , Multivariate Analysis , Prospective Studies , Pyridines/therapeutic use , Reoperation , Retrospective Studies , Risk Factors
6.
Am J Cardiol ; 105(10): 1426-32, 2010 May 15.
Article in English | MEDLINE | ID: mdl-20451689

ABSTRACT

Chronic right ventricular apical pacing (RVAP) has been associated with negative hemodynamic and clinical effects. The aim of the present study was to compare RVAP with right ventricular septal pacing (RVSP) in terms of echocardiographic features and clinical outcomes. A total of 93 patients without structural heart disease and with an indication for a permanent pacemaker were randomly assigned to receive a screw-in lead either in the RV apex (n = 46) or in the RV mid-septum (n = 47). The patients were divided into 3 subgroups according to the percentage of ventricular pacing: control group (n = 21, percentage of ventricular pacing < or =10%), RVAP group (n = 28), or RVSP group (n = 32; both latter groups had a percentage of ventricular pacing >10%). The RVAP group had more intraventricular dyssynchrony and a trend toward a worse left ventricular ejection fraction compared to the RVSP and control groups at 12 months of follow-up (maximal delay to peak systolic velocity between any of the 6 left ventricular basal segments was 57.8 +/- 38.2, 35.5 +/- 20.6, and 36.5 +/- 17.8 ms for RVAP, RVSP, and control group, respectively; p = 0.006; mean left ventricular ejection fraction 62.9 +/- 7.9%, 66.5 +/- 7.2%, and 66.6 +/- 7.2%, respectively, p = 0.14). Up to 48.1% of the RVAP patients showed significant intraventricular dyssynchrony compared to 19.4% of the RVSP patients and 23.8% of the controls (p = 0.04). However, no overt clinical benefits from RVSP were found. In conclusion, RVAP was associated with increased dyssynchrony compared to the RVSP and control patients. RVSP could represent an alternative pacing site in selected patients to reduce the harmful effects of traditional RVAP.


Subject(s)
Cardiac Pacing, Artificial/methods , Heart Ventricles , Pacemaker, Artificial , Ventricular Septum , Aged , Aged, 80 and over , Analysis of Variance , Atrioventricular Block/diagnostic imaging , Atrioventricular Block/therapy , Chi-Square Distribution , Echocardiography/methods , Electrocardiography , Equipment Design , Equipment Safety , Female , Follow-Up Studies , Humans , Male , Middle Aged , Probability , Prospective Studies , Risk Assessment , Sick Sinus Syndrome/diagnostic imaging , Sick Sinus Syndrome/therapy , Single-Blind Method , Treatment Outcome
7.
Rev. méd. Urug ; 6(1): 34-47, 1982. ilus, tab
Article in Spanish | LILACS | ID: lil-203470

ABSTRACT

6027 personas de siete poblaciones de "alto riesgo" en hidatidosis, del medio rural uruguayo, fueron sometidas a una encuesta epidemiológica y a relevamientos ecográficos hepáticos. Las encuestas demostraron que las condiciones siguen dadas para el automantenimiento de la enfermedad. El seguimiento y confirmación quirúrgica de la hidatidosis hepática en las personas con imágenes quísticas positivas, lleva a establecer un índice promedio de prevalencia en las poblaciones examinadas de 13,9 por mil. En 3593 microrradiografías realizadas concomitantemente no se encontraron quistes pulmonares. El predominio de las imágenes hialinas hepáticas en todos los grupos etarios nos habilita a afirmar que la enfermedad continúa siendo adquirida a lo largo de toda la vida. La frecuencia y el riesgo relativo son tanto mayores en el sexo masculino y a medida que aumenta la edad. El ultrasonido es un método idóneo para lograr su diagnóstico precoz. La existencia de un alto número de imágenes hialinas pequeñas(<5cm.) intrahepáticas, no pasibles de tratamiento quirúrgico llevó a establecer una instancia de vigilancia clínica y ecográfica sobre ellas. Este estudio nos permite reflejar con mejores bases la real prevalencia de la hidatidosis en aquellas poblaciones expuestas, llegar al diagnóstico en la etapa más útil antes de que aparezcan complicaciones y establecer un plan proyectivo para englobar a toda la campaña de este programa de atención primara en salud


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Echinococcosis , Uruguay , Echinococcosis , Echinococcosis, Pulmonary , Echinococcosis, Hepatic
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