Naveen Thuramalla
Ithaca College
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Featured researches published by Naveen Thuramalla.
Pediatric Critical Care Medicine | 2008
Nikolai M. Krivitski; Victor V. Kislukhin; Naveen Thuramalla
Objectives: No simple method exists for repeatedly measuring cardiac output in intensive care pediatric and neonatal patients. The purpose of this study is to present the theory and examine the in vitro accuracy of a new ultrasound dilution cardiac output measurement technology in which an extracorporeal arteriovenous tubing loop is inserted between existing arterial and venous catheters. Design: Laboratory experiments. Setting: Research laboratory. Subjects: None. Interventions: None. Measurements and Main Results: In vitro validations of cardiac output, central blood volume, total end-diastolic volume, and active circulation volume were performed in a model mimicking pediatric (children 2–10 kg) and neonatal (0.5–3 kg) flows and volumes against flows and volumes measured volumetrically. Reusable sensors were clamped onto the arterial and venous limbs of the arteriovenous loop. A peristaltic pump was used to circulate liquid at 6–12 mL/min from the artery to the vein through the arteriovenous loop. Body temperature injections of isotonic saline (0.3–10 mL) were performed. In the pediatric setting, the absolute difference between cardiac output measured by dilution and cardiac output measured volumetrically was 3.97% ± 2.97% (range 212–1200 mL/min); for central blood volume the difference was 4.59% ± 3.14% (range 59–315 mL); for total end-diastolic volume the difference was 4.10% ± 3.08% (range 24–211 mL); and for active circulation volume the difference was 3.30% ± 3.07% (range 247–645 mL). In the neonatal setting the difference for cardiac output was 4.40% ± 4.09% (range 106–370 mL/min); for central blood volume the difference was 4.90% ± 3.69% (range 50–62 mL); and for active circulation volume the difference was 5.39% ± 4.42% (range 104–247 mL). Conclusions: In vitro validation confirmed the ability of the ultrasound dilution technology to accurately measure small flows and volumes required for hemodynamic assessments in small pediatric and neonatal patients. Clinical studies are in progress to assess the reliability of this technology under different clinical situations.
Resuscitation | 2012
Alessio Vigani; Andre Shih; Patricia Queiroz; Romain Pariaut; Andrea Gabrielli; Naveen Thuramalla; Carsten Bandt
OBJECTIVEnNew volumetric variables of preload, such as total end-diastolic volume index (TEDVI) and active circulation volume index (ACVI) and central blood volume index (CBVI), may represent good indicators of preload and predictors of fluid responsiveness. During acute changes of intravascular volume these variables would allow a more accurate intervention.nnnAIMnThe aim of the present study was to investigate the changes in TEDVI, ACVI, CBVI in a juvenile model of hemorrhagic shock and resuscitation.nnnMETHODSnTwelve anaesthetized ponies (3-8 months of age) were studied at normovolaemia (BASE), after blood withdrawal to mean arterial pressure (MAP) of 40 mmHg (HEMO), after infusion of norepinephrine to reach a MAP of ± 10% of baseline (HE-NE), and after retransfusion of shed blood (RESU). TEDVI, ACVI, CBVI were measured by Ultrasound Dilution (UD) technology with CoStatus device. Data were analyzed using 1-way (ANOVA) followed by Bonferronis multiple pairwise comparisons. Evaluation of dependence between CoStatus volumetric variables and stroke volume index (SVI) were performed using the linear regression analysis and calculating the r(2) coefficient of determination.nnnRESULTSnTEDVI and ACVI changed significantly during HEMO and RESU status. NE administration induced MAP and CVP significant changes, whereas TEDVI and ACVI remained unchanged. CBVI showed high variability and seemed to be inconsistent on the identification of the volume status. In the correlation analysis, only TEDVI consistently correlated with SVI and volume induced SVI changes.nnnCONCLUSIONSnIn this animal model, TEDVI and ACVI were superior to CBVI in consistently reflecting hemorrhage. TEDVI but not ACVI and CBVI correlated with volume-induced changes in SVI. NE administration did not affect this correlation.
Veterinary Anaesthesia and Analgesia | 2011
Andre Shih; Steeve Giguère; Alessio Vigani; Renata Shih; Naveen Thuramalla; Carsten Bandt
OBJECTIVEnThe purpose of this study was to compare CO measured by use of lithium dilution (LiDCO) and ultrasound velocity dilution (UDCO) in a canine model of acute hemorrhage.nnnSTUDY DESIGNnProspective descriptive evaluation.nnnANIMALSnTwelve dogs (15-34 kg).nnnMETHODSnDogs were anesthetized and instrumented to measure direct blood pressure, heart rate, arterial blood gases and CO. The CO was measured by use of LiDCO and UDCO techniques. Measurements were obtained from each animal at baseline and during a low CO state (hemorrhagic state). Measurements were converted to cardiac index (CI = CO/BSA) values for statistical analysis. To measure CO using UDCO, a 20 mL bolus of 0.9% sodium chloride was administered and CO was calculated from the transient dilution of blood proteins created by the injection bolus. Hypovolemia was induced by withdrawing 40% of the blood volume until the mean arterial blood pressure (MAP) was stable at 40 mmHg for 10 minutes. Agreement was determined using Bland & Altman analysis and concordance correlation coefficients.nnnRESULTSnTwenty-four comparisons were made. Lithium determinations of CI ranged between 7.5 and 1.3 L minute(-1) m(-2), and the mean overall difference between the two methods was -0.40 L minute(-1) m(-2). The mean relative bias was -17 ± 21% (limits of agreements: -59% to 25%). There was no significant effect of state of CI on bias or relative bias (p = 0.24 and p = 0.10, respectively). The concordance correlation coefficient between LiDCO and UDCO as 0.88 (p < 0.0001).nnnCONCLUSIONSnWhen compared to lithium dilution, the UDCO technique is a viable method for measuring cardiac output in a model of normovolemia and hypovolemia in dogs.
Archives of Disease in Childhood | 2012
Nikolai M. Krivitski; Victor V. Kislukhin; Naveen Thuramalla; A Kriksunov
Background and Aims Major challenge for treatment of Hypoplastic left heart syndrome by Norwood procedure is in achieving the adequate Qp/Qs value. The absence of routine method of assessing the Qp/Qs value can lead to hypoxia, brain injury, for Qp/Qs< < 1 or to insufficient tissue perfusion and lung edema for Qp/Qs>>1. The aim of the study was to develop routine method for Qp/Qs assessment for PICU and NICU patients. Method development: A mathematical model of indicator movement for SV anatomy was developed. After intravenous injection and mixing in SV the first portion of the indicator enters systemic circulation via aorta. Second portion of the indicator enters lungs via PA, then again enters SV via left atria etc. The model suggests that Qp/Qs may be calculated from dilution curve (Pic.1) Qp/Qs=S2/S1. Results COstatus monitor, (Transonic Systems Inc., NY, USA) was used in NICU and PICU patients to measures cardiac output, blood volumes and to identify shunts and PDA. According to Transonic curve data archive recoded by COstatus for single ventricle patients the actual shape of dilution curves (example, Pic.2) well agrees with model data. Abstract 782 Figure 1 Dilution Curve Model Abstract 782 Figure 2 SV Patient Dilution Curve Conclusions Mathematical model for indicator movement in SV anatomy proved that Qp/Qs value can be calculated from indicator dilution curve. Next step is to validate the Qp/Qs values measured by COstatus in animal model and in patients. Grant NIH SBIR # R43 HL111852–01.
Archive | 2013
Nikolai M. Krivitski; Victor V. Kislukhin; Naveen Thuramalla; Anton Kriksunov
Archive | 2006
Nikolai M. Krivitski; Naveen Thuramalla
Pediatric Critical Care Medicine | 2014
Nikolai M. Krivitski; G. Galyanov; Naveen Thuramalla
Archive | 2014
Nikolai M. Krivitski; Naveen Thuramalla; Gregory Galyanov
Archive | 2008
Naveen Thuramalla; Nikolai M. Krivitski; Mark Alsberge
The FASEB Journal | 2007
Michael F. Callahan; Victor Kislukhin; Naveen Thuramalla; Nikolai M. Krivitski; Thomas L. Smith