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Biomedical subjects

Balachundhar Subramaniam

Publications and source records attributed to Balachundhar Subramaniam.

8 recordsLinked to original sources
PubMed2006

Transesophageal echocardiographic assessment of right atrial appendage anatomy and function: comparison with the left atrial appendage and implications for local thrombus formation.

OBJECTIVES: We sought to define right atrial appendage (RAA) anatomic and functional parameters in a consecutive series of participants and to compare these measures with left atrial appendage (LAA) indices among patients with in sinus rhythm and atrial fibrillation (AF). BACKGROUND: With AF, both atria are fibrillating, yet the vast majority of thrombi are located within the LAA. Transesophageal echocardiography provides anatomic and functional information regarding both the LAA and the RAA. METHODS: In a consecutive series of 92 patients (48 men; age 61 +/- 17 years) referred for transesophageal echocardiography, RAA and LAA anatomy (width, length, area) and ejection velocity were measured at two orientations (RAA, 90 and 135 degrees; LAA, 0 and 90 degrees). RESULTS: RAA anatomic measures were similar for both imaging planes, whereas LAA area was larger at 90 degrees. There was a modest correlation between RAA and LAA anatomic measures (area: r = 0.58, P = .001). RAA neck width was substantially greater than LAA neck width (P < .0001) whereas appendage area was similar (P = not significant) and RAA neck width/area was greater than LAA neck width/area (P < .0001). AF was associated with approximately 50% decline in ejection velocity for both the LAA and the RAA with an increase in LAA area (P = .006 vs sinus), but similar anatomic remodeling was not found for the RAA (P = not significant vs sinus). CONCLUSION: In this consecutive series of patients undergoing transesophageal echocardiography, RAA anatomic and functional parameters were found to be independent of imaging plane, with anatomic measures demonstrating a correlation with LAA measures. Although AF is associated with depressed RAA and LAA ejection velocities, anatomic RAA remodeling appears to be absent. The larger RAA width and lack of anatomic remodeling may partially explain the substantially lower prevalence of RAA thrombus found among patients with AF.

Adult↗
PubMed2006

Anesthetic management of pial synangiosis and intracranial hemorrhage with a Fontan circulation.

We report the case of a 11-year-old girl with Moyamoya syndrome, who had undergone staged-repair of tricuspid atresia to a Fontan circulation, scheduled to undergo bilateral pial synangiosis. Surgery for the first hemisphere was complicated by intracranial hemorrhage requiring an emergency craniotomy. The case highlights the importance of understanding Fontan physiology and its interrelationship with the cerebral circulation in the setting of cerebrovascular insufficiency and raised intracranial pressure.

Anesthesia, Intravenous↗
PubMed2005

Perioperative and long-term morbidity and mortality after above-knee and below-knee amputations in diabetics and nondiabetics.

We performed a retrospective review of a vascular surgery quality assurance database to evaluate the perioperative and long-term morbidity and mortality of above-knee amputations (AKA, n = 234) and below-knee amputations (BKA, n = 720) and to examine the effect of diabetes mellitus (DM) (181 of AKA and 606 of BKA patients). All patients in the database who had AKA or BKA from 1990 to May 2001 were included in the study. Perioperative 30-day cardiac morbidity and mortality and 3-yr and 10-yr mortality after AKA or BKA were assessed. The effect of DM on 30-day cardiac outcome was assessed by multivariate logistic regression and the effect on long-term survival was assessed by Cox regression analysis. The perioperative cardiac event rate (cardiac death or nonfatal myocardial infarction) was at least 6.8% after AKA and at most 3.6% after BKA. Median survival was significantly less after AKA (20 mo) than BKA (52 mo) (P < 0.001). DM was not a significant predictor of perioperative 30-day mortality (odds ratio, 0.76 [0.39-1.49]; P = 0.43) or 3-yr survival (Hazard ratio, 1.03 [0.86-1.24]; P = 0.72) but predicted 10-yr mortality (Hazard ratio, 1.34 [1.04-1.73]; P = 0.026). Significant predictors of the 30-day perioperative mortality were the site of amputation (odds ratio, 4.35 [2.56-7.14]; P < 0.001) and history of renal insufficiency (odds ratio, 2.15 [1.13-4.08]; P = 0.019). AKA should be triaged as a high-risk surgery while BKA is an intermediate-risk surgery. Long-term survival after AKA or BKA is poor, regardless of the presence of DM.

Adrenergic beta-Antagonists↗
PubMed2004

Ketamine as adjuvant analgesic to opioids: a quantitative and qualitative systematic review.

Animal studies on ketamine and opioid tolerance have shown promising results. Clinical trials have been contradictory. We performed a systematic review of randomized, double-blind clinical trials of ketamine added to opioid analgesia. Thirty-seven trials with 51 treatment arms and 2385 patients were included. Studies were divided into 5 subgroups: IV ketamine as single dose (n = 11), continuous infusion (n = 11), patient-controlled analgesia (PCA) (n = 6), epidural ketamine with opioids (n = 8), and studies in children (n = 4). Outcome measures included pain scores, time to first request for analgesia, supplemental analgesics, and adverse events. Efficacy was estimated by statistical significance (P < 0.05) of outcome measures as reported in studies and also by calculation of weighted mean difference for pain scores during the first 24 h after surgery. As compared to morphine alone, IV PCA with ketamine and morphine did not improve analgesia. Intravenous infusion of ketamine decreased IV and epidural opioid requirements in 6 of 11 studies. A single bolus dose of ketamine decreased opioid requirements in 7 of 11 studies. Five of 8 trials with epidural ketamine showed beneficial effects. Adverse effects were not increased with small dose ketamine. We conclude that small dose ketamine is a safe and useful adjuvant to standard practice opioid-analgesia.

Adult↗