Saurabh Chaturvedi

Dr. Saurabh Chaturvedi


Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 February 2015 in Cytokine
Verified
Journal Article
Closed access
Narayan PrasadNarayan Prasad
Narayan Prasad
AJAkhilesh K Jaiswal
Akhilesh K Jaiswal
VAVikas Agarwal
Vikas Agarwal
BYBRIJESH YADAV
BRIJESH YADAV
RSRaj Kumar Sharma
Raj Kumar Sharma
ASAjay Singh
Ajay Singh

12 September 2018 in International Journal of Rheumatic Diseases
Verified
Journal Article
Closed access
PDF file
SCSaurabh Chaturvedi
Saurabh Chaturvedi
Durga Prasanna MisraDurga Prasanna Misra
Durga Prasanna Misra
NPNarayan Prasad
Narayan Prasad
KRKailash Rastogi
Kailash Rastogi
HSHarshit Singh
Harshit Singh
VAVikas Agarwal
Vikas Agarwal

16 November 2018 in Clinical Rheumatology
Verified
Journal Article
Closed access
PDF file
SASajal Ajmani
Sajal Ajmani
HSHarshit Singh
Harshit Singh
SCSaurabh Chaturvedi
Saurabh Chaturvedi
RMRavi Mishra
Ravi Mishra
MRMohit Kumar Rai
Mohit Kumar Rai
VAVikas Agarwal
Vikas Agarwal

1 June 2015 in Journal of Functional Foods
Verified
Journal Article
Closed access
MRMinakshi Rana
Minakshi Rana
SRSukka Santosh Reddy
Sukka Santosh Reddy
PMPreeti Maurya
Preeti Maurya
VSVishal Singh
Vishal Singh
SCSaurabh Chaturvedi
Saurabh Chaturvedi
MBManoj Kumar Barthwal
Manoj Kumar Barthwal

27 July 2016 in Clinical Kidney Journal
Verified
Journal Article
Open access
PDF file
Narayan PrasadNarayan Prasad
Narayan Prasad
AJAkhilesh Jaiswal
Akhilesh Jaiswal
VAVikas Agarwal
Vikas Agarwal
SKShashi Kumar
Shashi Kumar
SCSaurabh Chaturvedi
Saurabh Chaturvedi
AKAnupama Kaul
Anupama Kaul
We aimed to longitudinally analyse changes in the levels of serum fibroblast growth factor 23 (FGF23), intact parathyroid hormone (iPTH) and associated minerals in patients undergoing renal transplantation. Sixty-three patients with end-stage renal disease (ESRD) who underwent living donor transplantation were recruited. Serum FGF23, iPTH, uric acid, inorganic phosphorous (iP), blood urea nitrogen and serum creatinine were measured pre-transplant and at 1 (M1), 3 (M3) and 12 months (M12) post-transplantation. FGF23 levels were decreased at M1, M3 and M12 by 93.81, 96.74 and 97.53%, respectively. iPTH levels were decreased by 67.95, 74.95 and 84.9%, respectively. The prevalence of hyperparathyroidism at M1, M3 and M12 post-transplantation was 63.5, 42.9 and 11.1%, respectively. FGF23 and iP levels remained above the normal range in 23 (36.5%) and 17 (27%) patients at M1, 10 (15.9%) and 5 (8%) at M3 and in none at M12 post-transplantation, respectively. A multivariate regression model revealed that, pre-transplant, iP was positively associated with iPTH (P = 0.016) but not with FGF 23; however, post-transplant, iP level was negatively associated with FGF23 (P < 0.001) but not with iPTH. Post-transplant FGF23 levels settle faster than those of iPTH. However, 11% of patients continued to have hyperparathyroidism even after 12 months.

1 August 2018 in Indian Journal of Critical Care Medicine
Verified
Journal Article
Open access
SCSaurabh Chaturvedi
Saurabh Chaturvedi
PMPrabhaker Mishra
Prabhaker Mishra
RMRavi Mishra
Ravi Mishra
PGPralay Shankar Ghosh
Pralay Shankar Ghosh
HSHarshit Singh
Harshit Singh
RSRatender Kumar Singh
Ratender Kumar Singh
Neutrophil CD64 (nCD64) has been found to identify sepsis from nonseptic patients. It is also reported to be a predictor of survival and severity of sepsis. The goal of this study was to correlate serial nCD64 with Intensive Care Unit (ICU) outcome and severity of sepsis. A prospective observational study was conducted in 12-bedded critical care unit of a tertiary care center. Adult patients with sepsis were included in this study. Demographics, illness severity scores, clinical parameters, laboratory data, and 28-day outcome were recorded. Serial nCD64 analysis was done (on days 0, 4, and 8) in consecutive patients. Fifty-one consecutive patients were included in the study. Median Acute Physiology and Chronic Health Evaluation II was 16 (12-20) and mean Sequential Organ Failure Assessment was 9 (8-10). Compared to survivors, nonsurvivors had higher nCD64 on day 8 (P = 0.001). nCD64 was higher in the septic shock group compared to sepsis group on days 0 and 8 (P < 0.05). Survivors showed improving trend of nCD64 over time while nonsurvivors did not. This trend was similar in the presence or absence of septic shock. nCD64 count was a good predictor of the septic shock on day 0 (area under the curve [AUC] = 0.747, P = 0.010) and moderate predictor at day 8 (AUC = 0.679, P = 0.028). Monitoring serial nCD64 during ICU stay may be helpful in determining the clinical course of septic patients.