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1.
Chest ; 160(3): 909-918, 2021 09.
Article in English | MEDLINE | ID: mdl-33819472

ABSTRACT

BACKGROUND: Long-term cognitive impairment frequently occurs after critical illness; no treatments are known to improve long-term cognition. RESEARCH QUESTION: Does a single high-dose (540,000 International Units) enteral treatment of vitamin D3 given shortly after hospital admission in critically ill patients who are vitamin D deficient improve long-term global cognition or executive function? STUDY DESIGN AND METHODS: This study evaluated long-term cognitive outcomes among patients enrolled in a multicenter, blinded, randomized clinical trial comparing vitamin D3 treatment vs placebo in critically ill adults with vitamin D deficiency. Global cognition was measured by the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). Executive function was measured with a composite score derived from three Delis-Kaplan Executive Function System subscales. Outcomes were assessed at a median of 443 days (interquartile range, 390-482 days) after randomization and were compared using multivariate proportional odds regression. Adjusted ORs of > 1.0 would indicate better outcomes in the vitamin D3 group compared with the placebo group. RESULTS: Ninety-five patients were enrolled, including 47 patients randomized to vitamin D3 treatment and 48 patients randomized to placebo. The adjusted median RBANS score at follow-up was 79.6 (95% CI, 73.0-84.0) in the vitamin D3 group and 82.1 (95% CI, 74.7-84.6) in the placebo group (adjusted OR, 0.83; 95% CI, 0.50-1.38). The adjusted median executive function composite scores were 8.1 (95% CI, 6.8-9.0) and 8.7 (95% CI, 7.4-9.3), respectively (adjusted OR, 0.72; 95% CI, 0.36-1.42). INTERPRETATION: In vitamin D-deficient, critically-ill adults, a large dose of enteral vitamin D3 did not improve long-term global cognition or executive function. TRIAL REGISTRY: ClinicalTrials.gov; No.: NCT03733418; URL: www.clinicaltrials.gov.


Subject(s)
Cholecalciferol/administration & dosage , Cognition/drug effects , Cognitive Dysfunction , Critical Illness , Executive Function/drug effects , Long Term Adverse Effects/drug therapy , Vitamin D Deficiency , Cognitive Dysfunction/diagnosis , Cognitive Dysfunction/drug therapy , Cognitive Dysfunction/etiology , Critical Illness/psychology , Critical Illness/rehabilitation , Female , Humans , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/etiology , Long Term Adverse Effects/psychology , Male , Middle Aged , Neuropsychological Tests , Pulse Therapy, Drug/methods , Treatment Outcome , Vitamin D Deficiency/drug therapy , Vitamin D Deficiency/psychology , Vitamins/administration & dosage
2.
Geriatr Gerontol Int ; 19(8): 815-822, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31267646

ABSTRACT

AIM: We investigated the long-term risk of dementia for up to 10 years in patients with stroke and broadened the correlates. METHODS: We carried out a case-control study using the Taiwan National Health Insurance Research database in 2000 with a sampled population of 1 million. The study cohort comprised 8236 patients with stroke and no dementia history. We carried out a 1:1 case-control matched analysis on estimated propensity scores. Cox proportional hazards regressions were carried out to estimate the risk of dementia during the 5- and 10-year follow-up periods. The risk factors were also investigated. RESULTS: The stroke cohort was significantly at more risk of dementia during the 5- and 10-year follow-up periods, with adjusted hazard ratios 1.87 and 1.53, respectively. The patients with ischemic stroke, transient ischemic attack and intracerebral hemorrhage had a significantly higher risk of dementia after 5 and 10 years, with adjusted hazard ratios of 1.81 and 1.49, 1.92 and 1.61, and 2.14 and 1.61, respectively. The significant risk factors of dementia were age ≥60 years, resident in southern and eastern regions, having low insurance range, and antiplatelet use. CONCLUSIONS: Stroke and the subtypes, including ischemic stroke, transient ischemic attack and intracerebral hemorrhage, increase the long-term risk of dementia. The incidence of post-stroke dementia increases yearly, but the relative risk decreases gradually. Older adults, residents in southern and eastern regions, having low insurance range and antiplatelet use were prominent risk factors of post-stroke dementia in Taiwan. Careful management of stroke and risk factors of post-stroke dementia with long-term follow up of cognition should be reinforced. Geriatr Gerontol Int 2019; 19: 815-822.


Subject(s)
Brain Ischemia , Cerebral Hemorrhage , Dementia , Ischemic Attack, Transient , Long Term Adverse Effects , Stroke , Age Factors , Aged , Brain Ischemia/complications , Brain Ischemia/epidemiology , Case-Control Studies , Cerebral Hemorrhage/complications , Cerebral Hemorrhage/epidemiology , Dementia/diagnosis , Dementia/epidemiology , Dementia/etiology , Female , Humans , Incidence , Ischemic Attack, Transient/complications , Ischemic Attack, Transient/epidemiology , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/epidemiology , Male , Middle Aged , National Health Programs/statistics & numerical data , Proportional Hazards Models , Risk Factors , Stroke/diagnosis , Stroke/epidemiology , Stroke/etiology , Taiwan/epidemiology
3.
Dis Colon Rectum ; 61(11): 1316-1319, 2018 11.
Article in English | MEDLINE | ID: mdl-30239390

ABSTRACT

BACKGROUND: Full-thickness rectal prolapse has a significant negative impact on quality of life. The therapeutic options, specifically in elderly patients, are imperfect. Perineal stapled rectal prolapse resection is a novel operation for treating external rectal prolapse. Long-term follow-up following this procedure is lacking. In our study, we report a long-term follow-up of 30 patients, analyzing the long-term recurrence rate, morbidity, and functional outcome. OBJECTIVE: This study aimed to examine the long-term results of perineal stapled rectal resection in a population unfit for prolonged general anesthesia. DESIGN: This was a cohort study with a prospective follow-up. SETTINGS: This study was conducted at a single tertiary referral center. PATIENTS: Patients undergoing perineal stapled rectal resection from January 2010 to June 2013 were included. INTERVENTIONS: Perineal stapled rectal prolapse resection was performed. MAIN OUTCOME MEASURES: The primary outcome measured was prolapse recurrence. RESULTS: A total of 30 patients underwent the surgical intervention. The median follow-up period was 61 months (range, 37-65). No intraoperative or postoperative complications occurred. Six patients (20%) had recurrent rectal prolapse, and continence was not achieved in any of the patients. Two patients who had recurrence underwent a redo perineal stapled rectal resection. LIMITATIONS: This study was limited by the small cohort of selected patients. CONCLUSIONS: Frail patients that can only endure a short procedure under regional anesthesia should be considered for perineal stapled rectal prolapse resection. The lack of mortality and morbidity, specifically in this population, along with the low long-term recurrence rates, make this a favorable surgical alternative. See Video Abstract at http://links.lww.com/DCR/A745.


Subject(s)
Colectomy , Long Term Adverse Effects , Postoperative Complications , Quality of Life , Rectal Prolapse , Surgical Stapling , Aged , Aged, 80 and over , Cohort Studies , Colectomy/adverse effects , Colectomy/methods , Female , Follow-Up Studies , Humans , Israel/epidemiology , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/psychology , Male , Perineum/surgery , Postoperative Complications/diagnosis , Postoperative Complications/psychology , Rectal Prolapse/epidemiology , Rectal Prolapse/psychology , Rectal Prolapse/surgery , Recurrence , Surgical Stapling/adverse effects , Surgical Stapling/methods , Treatment Outcome
4.
Int J Colorectal Dis ; 33(10): 1341-1348, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29934702

ABSTRACT

PURPOSE: The aim of the study was to assess the long-term outcome of a Malone antegrade continence enema (MACE) procedure for fecal incontinence or constipation in adults. METHODS: This retrospective single-center study assessed the long-term outcome and quality of life (QoL) of patients who underwent a MACE procedure between 2005 and 2014 at the Maastricht University Medical Centre. Success rate was quantified by using Malone's continence scale. Quality of life was assessed by validated questionnaires covering general quality of life (SF-36 and Karnofsky scale), current pain level (visual analog scale), fecal incontinence (Vaizey incontinence survey), or constipation (Cleveland Clinic Constipation Score). RESULTS: Based on patients' records, 22 out of 30 patients (73%; 95% CI 54-87%) were still using their MACE. Mean follow-up was 43 months (SD 25.9) since time of surgery. According to the Malone continence scale, the overall success rate was 37% (95% CI 20.0-53.3). Nine patients developed a postoperative complication. Eighteen out of 22 patients (13 with constipation and 5 with fecal incontinence) returned the QoL questionnaires (82% response rate). Long-term quality of life of patients with a MACE did not differ from the general Dutch population. CONCLUSIONS: In our cohort of patients with fecal incontinence or constipation, MACE resulted in a disappointed overall success rate of 37%. However, it may be indicated in patients who do not prefer more invasive surgical procedures or a definite stoma. The success and morbidity rate should be thoroughly discussed with the patients preoperatively.


Subject(s)
Colostomy , Constipation , Enema , Fecal Incontinence , Long Term Adverse Effects , Quality of Life , Adult , Colostomy/adverse effects , Colostomy/methods , Colostomy/psychology , Constipation/physiopathology , Constipation/psychology , Constipation/therapy , Defecation/physiology , Enema/adverse effects , Enema/methods , Fecal Incontinence/physiopathology , Fecal Incontinence/psychology , Fecal Incontinence/therapy , Female , Humans , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/epidemiology , Long Term Adverse Effects/etiology , Long Term Adverse Effects/psychology , Male , Middle Aged , Netherlands , Outcome Assessment, Health Care , Pain/diagnosis , Pain/etiology , Pain Measurement/methods , Postoperative Complications/diagnosis , Postoperative Complications/epidemiology , Postoperative Complications/psychology , Retrospective Studies , Surveys and Questionnaires
5.
Angiol Sosud Khir ; 23(2): 82-87, 2017.
Article in Russian | MEDLINE | ID: mdl-28594800

ABSTRACT

The objective of the study was to compare safety and efficacy of rivaroxaban and dabigatran with warfarin in treatment of patients with acute venous thromboembolic complications (VTEC). The authors analysed the results of examining and treating a total of 95 patients presenting with VTEC and randomly divided into three groups. In all groups the initial anticoagulant therapy consisted in unfractionated heparin administered for 5 days, after which the patients followed by switching were switched to a 6-month course of treatment with oral anticoagulants. Patients from Group One received warfarin, Group Two patients were treated with dabigatran etexilate, and Group Three patients were treated with rivaroxaban. Relapses of the disease were diagnosed in 2 (5.7%) patients from Group One. Haemorrhagic complications were noted in 8 (22.9%) Group One patients, in 3 (10%) Group Two patients and in 2 (6.7%) Group Three patients. After the end of treatment, complete recanalization of the thrombosed veins was revealed 13 (37.1%) patients from Group One, in 15 (50%) patients from Group Two and in 14 (46.7%) patients from Group Three. One year after the end of treatment, freedom from chronic venous insufficiency was observed in 8 (23.3%) patients of Group One, in 12 (40%) patients of Group Two and in 11 (36.6%) patients of Group Three. The composite quality of life indices after the treatment course were (appeared to be) higher in Group Two and Three patients compared with those of Group One. Hence, a conclusion was drawn that dabigatran and rivaroxaban turned out to be superior by efficacy and safety to warfarin in treatment of this patient cohort. No statistically significant differences were observed while comparing dabigatran and rivaroxaban.


Subject(s)
Dabigatran , Long Term Adverse Effects , Rivaroxaban , Venous Thromboembolism , Warfarin , Acute Disease , Anticoagulants/administration & dosage , Anticoagulants/adverse effects , Dabigatran/administration & dosage , Dabigatran/adverse effects , Drug Monitoring/methods , Female , Humans , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/physiopathology , Long Term Adverse Effects/psychology , Male , Middle Aged , Quality of Life , Rivaroxaban/administration & dosage , Rivaroxaban/adverse effects , Treatment Outcome , Venous Thromboembolism/diagnosis , Venous Thromboembolism/drug therapy , Warfarin/administration & dosage , Warfarin/adverse effects
6.
Isr Med Assoc J ; 19(4): 246-250, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28480680

ABSTRACT

BACKGROUND: The very long-term prognostic significance of ventricular late potentials (VLP) in patients post ST-elevation myocardial infarction (STEMI) is unclear. OBJECTIVES: To evaluate the long-term predictive value of VLP for mortality post-STEMI. METHODS: We conducted serial signal-averaged electrocardiography (SAECG) measurements in 63 patients on the 1st, 2nd and 3rd day pre-discharge, and 30 days after STEMI in patients admitted in 2001. We followed the patients for 10 years and correlated the presence of VLP with all-cause and cardiovascular mortality. RESULTS: The mean age was 59.9 ± 12.3 years. Thrombolysis was performed in 41 patients (65%). Percutaneous coronary intervention was performed pre-discharge in 40 patients (63%) and coronary artery bypass grafting in 7 (11%). Five consecutive measurements to define the presence of VLP were obtained in 52 patients (21 with VLP and 31 without). We found a higher prevalence of VLP in males compared to females (QRS segment > 114 msec, 51% vs. 12%, P = 0.02, duration of the low amplitude signal < 40 mV) in the terminal portion of the averaged QRS complex > 38 msec, 47% vs. 25%, P = 0.05). Over 10 years of follow-up, 14 (22%) patients died, 10 (70%) due to cardiovascular non-arrhythmic complications, 6 with VLP compared to only 3 without (28.6% vs. 9.7%, P = 0.125, hazard ratio = 2.96, confidence intervals = 0.74-11.84) (are these numbers meant to total 10?). CONCLUSIONS: Over 10 years of follow-up, the presence of VLP in early post-STEMI is not predictive of arrhythmic or non-arrhythmic cardiovascular mortality.


Subject(s)
Electrophysiologic Techniques, Cardiac , Heart Ventricles/physiopathology , Long Term Adverse Effects , ST Elevation Myocardial Infarction , Aged , Electrocardiography/methods , Electrocardiography/statistics & numerical data , Electrophysiologic Techniques, Cardiac/methods , Electrophysiologic Techniques, Cardiac/statistics & numerical data , Female , Follow-Up Studies , Humans , Israel/epidemiology , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/epidemiology , Male , Middle Aged , Percutaneous Coronary Intervention/adverse effects , Percutaneous Coronary Intervention/statistics & numerical data , Predictive Value of Tests , Prevalence , Prognosis , Risk Factors , ST Elevation Myocardial Infarction/complications , ST Elevation Myocardial Infarction/diagnosis , ST Elevation Myocardial Infarction/mortality , ST Elevation Myocardial Infarction/physiopathology , Sex Factors , Thrombolytic Therapy/adverse effects , Thrombolytic Therapy/statistics & numerical data
7.
Bipolar Disord ; 19(1): 41-49, 2017 02.
Article in English | MEDLINE | ID: mdl-28239952

ABSTRACT

OBJECTIVE: Magnetic resonance imaging (MRI) studies in bipolar I disorder (BD-I) suggest that lithium is associated with increased volumes of cortico-limbic structures. However, more rigorous control of confounding factors is needed to obtain further support for this hypothesis. The aim of the present study was to assess differences in brain volumes among long-term lithium-treated BD-I patients, unmedicated BD-I patients, and healthy controls. METHODS: This was a cross-sectional study with 32 euthymic BD-I patients (16 on lithium monotherapy for a mean of 180 months, and 16 receiving no medication for at least the 2 months prior to the study) and 20 healthy controls. Patients were euthymic (Hamilton Depression Rating Scale [HDRS] <6 and Young Mania Rating Scale [YMRS] <7) and had not taken psychotropic medications other than lithium for at least 6 months. Brain images were acquired on a 1.5 Tesla MRI (Phillips, Amsterdam, The Netherlands) and segmented to generate volumetric measures of cortical and subcortical brain areas, ventricles and global brain. RESULTS: Significant differences were found in the volumes of the left amygdala (P=.0003), right amygdala (P=.030), left hippocampus (P=.022), left thalamus (P=.022), and right thalamus (P=.019) in long-term lithium-treated BD-I patients, compared to unmedicated patients and controls, after multivariable adjustment. No differences were observed in global brain volume or in ventricular size among the three groups. Likewise, there was no correlation between serum lithium levels and the increase in size in the described brain areas. CONCLUSIONS: The structural differences found among the three groups, and specifically those between long-term lithium-treated and unmedicated BD-I patients, indicate increased limbic structure volumes in lithium-treated patients.


Subject(s)
Amygdala , Bipolar Disorder , Hippocampus , Lithium , Long Term Adverse Effects , Thalamus , Adult , Amygdala/diagnostic imaging , Amygdala/drug effects , Amygdala/pathology , Antimanic Agents/administration & dosage , Antimanic Agents/adverse effects , Bipolar Disorder/diagnosis , Bipolar Disorder/drug therapy , Cross-Sectional Studies , Female , Healthy Volunteers , Hippocampus/diagnostic imaging , Hippocampus/drug effects , Hippocampus/pathology , Humans , Lithium/administration & dosage , Lithium/adverse effects , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/etiology , Magnetic Resonance Imaging/methods , Male , Middle Aged , Netherlands , Organ Size/drug effects , Thalamus/diagnostic imaging , Thalamus/drug effects , Thalamus/pathology
8.
Heart Rhythm ; 13(11): 2174-2180, 2016 11.
Article in English | MEDLINE | ID: mdl-27544746

ABSTRACT

BACKGROUND: Atrial arrhythmias may still occur in patients after durable pulmonary vein isolation (PVI). OBJECTIVE: The purpose of this study was to examine the incidence of patients undergoing ablation for recurrent arrhythmia despite chronic PVI and their clinical outcomes. METHODS: Patients undergoing repeat left atrial ablation procedures were selected from a prospective registry. From this population, we identified patients with chronic PVI. Clinical characteristics, ablation strategies, and outcomes were analyzed. RESULTS: Between January 2003 and December 2013, 1045 patients underwent 1298 repeat left atrial procedures. Of these, 900 patients had atrial fibrillation (AF) and 145 had atrial flutter (AFL)/atrial tachycardia (AT). Fifty-two patients (5.0%; 27 with AF and 25 with AFL/AT) had chronic PVI and were included in the study. Patients were followed for 19.7 ± 5.6 months. In patients with AF, 11 (41%) had a non-PV trigger identified. Ablation strategies included non-PV trigger ablation (n = 11), empiric trigger-site ablation (n = 3), provoked arrhythmia ablation (n = 9), complex fractionated atrial electrogram ablation (n = 2), and linear ablation (n = 2). During follow-up, 9 (33%) had no recurrence, 7 (26%) had rare AF (≤2 episodes during follow-up ≥1 year), and 11 (41%) had AF recurrence. In patients with AFL/AT, 12 (48%) had no recurrence, 4 (16%) had rare recurrence (≤2 episodes during follow-up ≥1 year), and 9 (36%) had recurrence. CONCLUSION: In patients with PVI undergoing a repeat procedure during the time period studied, only a small portion had chronic PVI. A strategy of targeting non-PV triggers for AF and linear/focal ablation for AFL/AT may achieve long-term arrhythmia control in the majority of patients.


Subject(s)
Atrial Fibrillation , Atrial Flutter , Catheter Ablation , Long Term Adverse Effects , Pulmonary Veins/surgery , Reoperation , Aged , Anti-Arrhythmia Agents/therapeutic use , Atrial Fibrillation/diagnosis , Atrial Fibrillation/epidemiology , Atrial Fibrillation/physiopathology , Atrial Fibrillation/surgery , Atrial Flutter/diagnosis , Atrial Flutter/epidemiology , Atrial Flutter/physiopathology , Catheter Ablation/adverse effects , Catheter Ablation/methods , Electrophysiologic Techniques, Cardiac/methods , Female , Heart Conduction System/physiopathology , Humans , Incidence , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/epidemiology , Long Term Adverse Effects/physiopathology , Long Term Adverse Effects/surgery , Male , Middle Aged , Pennsylvania , Recurrence , Reoperation/methods , Reoperation/statistics & numerical data
9.
Heart Rhythm ; 13(11): 2151-2158, 2016 11.
Article in English | MEDLINE | ID: mdl-27453126

ABSTRACT

BACKGROUND: Catheter ablation in the right ventricular outflow tract (RVOT) may modify the electrophysiologic substrate for recurrent ventricular tachycardia/ventricular fibrillation (VT/VF) in patients with Brugada syndrome (BrS). OBJECTIVE: The purpose of this study was to investigate the mechanism and arrhythmogenic substrate of VT/VF and to evaluate the long-term outcomes of catheter ablation in patients with BrS. METHODS: Eleven consecutive patients with BrS referred to 2 academic medical centers underwent combined epicardial-endocardial electroanatomic mapping. Catheter ablation was performed in regions of localized conduction slowing. Transmural dispersion of late activation was calculated as the difference between the latest activation between epicardium and endocardium, and low-voltage areas were analyzed. RESULTS: Eleven patients met diagnostic criteria for BrS (spontaneous type 1, n = 9; Na channel provocation = 2). All patients were found to have a localized region in the anterior epicardial RVOT with conduction slowing evidenced by prolonged electrogram duration (78.79 ± 19.87 ms vs 58.93 ± 10.11 ms in epicardial right ventricle, and 59.87 ± 12.61 ms in endocardial RVOT, P <.005, respectively) with variable low voltage (0.97 ± 0.48 mV; median scar area 19.8 ± 25.9 cm2). Epicardial ablation resulted in normalization of spontaneous type 1 Brugada ECG pattern in all patients, and 73% were free from VT/VF at 25 ± 11 months. CONCLUSION: Prolonged electrograms localized to epicardial RVOT with variable low voltage were identified in all patients with BrS. J-point and ST-segment elevation correlated with greater transmural dispersion of late activation and was independent of total low-voltage area. Despite normalization of spontaneous type 1 pattern in all patients after ablation, recurrence was still observed, suggesting the implantable cardioverter-defibrillator as the cornerstone therapy for BrS.


Subject(s)
Brugada Syndrome , Catheter Ablation , Endocardium , Epicardial Mapping/methods , Heart Conduction System , Pericardium , Adult , Brugada Syndrome/complications , Brugada Syndrome/diagnosis , Brugada Syndrome/physiopathology , Brugada Syndrome/surgery , Catheter Ablation/adverse effects , Catheter Ablation/methods , China , Electrocardiography/methods , Electrophysiologic Techniques, Cardiac/methods , Endocardium/pathology , Endocardium/physiopathology , Female , Heart Conduction System/physiopathology , Heart Conduction System/surgery , Heart Ventricles/pathology , Heart Ventricles/physiopathology , Humans , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/physiopathology , Long Term Adverse Effects/prevention & control , Male , Middle Aged , Outcome and Process Assessment, Health Care , Pericardium/pathology , Pericardium/physiopathology , Recurrence , Tachycardia, Ventricular/diagnosis , Tachycardia, Ventricular/etiology , Tachycardia, Ventricular/physiopathology , Tachycardia, Ventricular/prevention & control , Ventricular Fibrillation/diagnosis , Ventricular Fibrillation/etiology , Ventricular Fibrillation/physiopathology , Ventricular Fibrillation/prevention & control
10.
Heart Rhythm ; 13(1): 141-9, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26304713

ABSTRACT

BACKGROUND: Whether ablation of non-pulmonary vein (PV) triggers after pulmonary vein antrum isolation (PVAI) improves the long-term procedure outcome in patients with paroxysmal atrial fibrillation (PAF) and left ventricular systolic dysfunction is unknown. OBJECTIVE: We sought to evaluate whether a more extensive ablation procedure improves outcomes at follow-up. METHODS: Consecutive patients with PAF refractory to antiarrhythmic drugs presenting for PVAI were prospectively studied. Patients were categorized into 2 groups: patients with left ventricular ejection fraction (LVEF) ≤35% (group I; n = 175) and patients with LVEF ≥50% (group II; n = 545). Patients in group I were further divided according to whether additional ablation of non-PV triggers was performed (group IA; n = 88) or not (group IB; n = 87). Long-term ablation success off antiarrhythmic drugs after a single procedure was analyzed. RESULTS: Patients in group I had more non-PV triggers than did patients in group II (69.1% vs 26.6%; P < .001). During a follow-up of 15.8 ± 4.7 months, fewer patients in group I remained free from recurrences than those in group II (53.7% vs 81.7%; P < .001). Long-term ablation success was higher in group IA than in group IB (75.0% vs 32.2%; P < .001) and similar to that in group II (75.0% vs 81.7%; P = .44). In multivariate analysis, LVEF ≤35% (hazard ratio 1.68; P = .003) and non-PV triggers (hazard ratio 3.12; P < .001) were independent predictors of recurrences. CONCLUSION: In patients with PAF and left ventricular systolic dysfunction, ablation of non-PV triggers in addition to PVAI significantly improves their long-term procedure outcome.


Subject(s)
Atrial Fibrillation , Catheter Ablation , Long Term Adverse Effects/prevention & control , Pulmonary Veins/surgery , Ventricular Dysfunction, Left , Aged , Anti-Arrhythmia Agents/therapeutic use , Atrial Fibrillation/diagnosis , Atrial Fibrillation/physiopathology , Atrial Fibrillation/surgery , Catheter Ablation/adverse effects , Catheter Ablation/methods , Electrophysiologic Techniques, Cardiac/methods , Female , Humans , Long Term Adverse Effects/diagnosis , Male , Middle Aged , Proportional Hazards Models , Prospective Studies , Recurrence , Stroke Volume , Treatment Outcome , Ventricular Dysfunction, Left/diagnosis , Ventricular Dysfunction, Left/physiopathology
11.
Indian J Pediatr ; 83(2): 126-30, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26223873

ABSTRACT

OBJECTIVE: To correlate the bone mineral parameters [bone mineral content (BMC) and bone mineral density (BMD)] using Dual energy X ray Absorptiometry (DXA) scan with anthropometric measurements and to study the effect of glucocorticoid therapy on BMC/BMD in children with Congenital adrenal hyperplasia (CAH). METHODS: A cross-sectional study was carried out in the Pediatric Endocrinology unit from January 2012 through March 2013 at Kanchi Kamakoti CHILDS Trust hospital, Chennai. Thirteen CAH children aged 0-132 mo with classic salt wasting due to 21 hydroxylase deficiency were included in the study. All children were treated with T.hydrocortisone @10-15 mg/m(2)/d twice daily and T. fludrocortisone 50 µg once daily orally at the time of enrollment into the study. The duration of glucocorticoid (hydrocortisone) treatment from the date of diagnosis till the time of enrollment into the study was noted and categorized as children receiving < 5 and > 5 y of glucocorticoid therapy. None received Vitamin D/calcium supplementation at the time of enrollment. BMC and areal BMD for the lumbar spine and total body less head (TBLH) were measured with Lunar DXA machine. RESULTS: The mean height, weight and BMI of children were 87.3 ± 33 cm, 13.49 ± 11.2 kg and 14 ± 4.07 kg/m(2) respectively. TBLH BMC was 369.14 ± 312.18 g and TBLH BMD was 0.63 ± 0.11 g/cm(2). There was a significant correlation between height and total body less head BMC/BMD in the index series [P < 0.05, significant]. The TBLH and spine BMD were also assessed with regards to the duration of glucocorticoid therapy and it has been observed that TBLH and spine BMD decreased with increased duration of steroid therapy (p < 0.05, significant). CONCLUSIONS: In the absence of normative data or z scores, BMC/BMD correlates well with height for age. Children who received more than 5 y of glucocorticoid treatment had lower TBLH and spine BMD scores and hence, calcium and Vitamin D supplementation should be considered.


Subject(s)
Adrenal Hyperplasia, Congenital/drug therapy , Bone Density/drug effects , Glucocorticoids , Long Term Adverse Effects , Absorptiometry, Photon/methods , Adrenal Hyperplasia, Congenital/epidemiology , Anthropometry/methods , Child , Child, Preschool , Cross-Sectional Studies , Female , Glucocorticoids/administration & dosage , Glucocorticoids/adverse effects , Humans , India/epidemiology , Long Term Adverse Effects/chemically induced , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/prevention & control , Male , Statistics as Topic
12.
BMC Geriatr ; 15: 149, 2015 Nov 17.
Article in English | MEDLINE | ID: mdl-26572609

ABSTRACT

BACKGROUND: The catabolic state that follows hip fracture contributes to loss of muscle mass and strength, that is sarcopenia, which impacts functional ability and health-related quality of life. Measures to prevent such long-term postoperative consequences are of important concern. The aim of this study was to evaluate the combined effects of protein-rich nutritional supplementation and bisphosphonate on body composition, handgrip strength and health-related quality of life following hip fracture. METHODS: The study included 79 men and women with hip fracture, mean age 79 years (SD 9), without severe cognitive impairment, who were ambulatory and living independently before fracture. Patients were randomized postoperatively to receive liquid supplementation that provided 40 g of protein and 600 kcal daily for six months after the fracture, in addition to bisphosphonates once weekly for 12 months (group N, n = 26), or bisphosphonates alone once weekly for 12 months (group B, n = 28). All patients, including the controls (group C, n = 25) received calcium 1 g and vitamin D3 800 IU daily. Body composition as measured by dual-energy X-ray absorptiometry (DXA), handgrip strength (HGS) and health-related quality of life (HRQoL) were registered at baseline, six and 12 months postoperatively. RESULTS: There were no differences among the groups regarding change in fat-free mass index (FFMI), HGS, or HRQoL during the study year. Intra-group analyses showed improvement of HGS between baseline and six months in the N group (P = 0.04). HRQoL decreased during the first year in the C and B groups (P = 0.03 and P = 0.01, respectively) but not in the nutritional supplementation N group (P = 0.22). CONCLUSIONS: Protein-rich nutritional supplementation was unable to preserve FFMI more effectively than vitamin D and calcium alone, or combined with bisphosphonate, in this relatively healthy group of hip fracture patients. However, trends toward positive effects on both HGS and HRQoL were observed following nutritional supplementation. TRIAL REGISTRATION: Clinicaltrials.gov NCT01950169 (Date of registration 23 Sept 2013).


Subject(s)
Dietary Proteins/administration & dosage , Diphosphonates/administration & dosage , Fracture Fixation , Hip Fractures , Postoperative Complications , Quality of Life , Sarcopenia , Vitamin D/administration & dosage , Absorptiometry, Photon/methods , Activities of Daily Living , Aged , Body Composition/drug effects , Bone Density Conservation Agents/administration & dosage , Dietary Supplements , Female , Fracture Fixation/adverse effects , Fracture Fixation/rehabilitation , Hand Strength , Hip Fractures/complications , Hip Fractures/rehabilitation , Hip Fractures/surgery , Humans , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/etiology , Long Term Adverse Effects/prevention & control , Long Term Adverse Effects/psychology , Male , Postoperative Complications/diagnosis , Postoperative Complications/prevention & control , Postoperative Complications/psychology , Sarcopenia/diagnosis , Sarcopenia/etiology , Sarcopenia/prevention & control , Sarcopenia/psychology
13.
Rev. enferm. neurol ; 11(3): 120-128, sep.- dic. 2012.
Article in Spanish | BDENF, LILACS | ID: biblio-1034708

ABSTRACT

La automedicación, es “el consumo de medicamentos, hierbas y remedios caseros por iniciativa o consejo de otra persona, sin consultar al médico”, considerada también como un fenómeno que se ha incrementado a través del tiempo, convirtiéndose en un serio problema de salud pública. En México no existen estudios o publicaciones que permitan valorar la real magnitud de esta práctica en la población. Objetivo: Conocer los factores que influyen en la automedicación del personal de enfermería a nivel técnico y estudiantes del Instituto Nacional de Neurología y Neurocirugía.


Self-medication, is “the use of drugs, herbs and home remedies or advice on the initiative of another person, without consulting a doctor”, also regarded as a phenomenon that has been increasing over time, becoming a serious public health problem. In Mexico, there are no studies or publications to assess the real magnitude of this practice in the population. Objective: Understanding the factors that influence self-medication nursing staff technical level, and students of the National Institute of Neurology and Neurosurgery.


Subject(s)
Humans , Self Medication/adverse effects , Self Medication/nursing , Self Medication/ethics , Self Medication/methods , Self Medication/mortality , Self Medication/standards , Long Term Adverse Effects/diagnosis , Long Term Adverse Effects/nursing , Long Term Adverse Effects/mortality , Long Term Adverse Effects/prevention & control , Nursing/standards , Nursing
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