Harini Bejjanki
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Harini Bejjanki has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Abhilash Koratala
Division of Nephrology, Medical College of Wisconsin, Milwaukee, Wisconsin
5 shared publications - Chintan Shah
Hematology and Oncology, University of Florida, Gainesville, USA
4 shared publications Rohit Bishnoi
Division of Hospital Medicine, University of Florida, Gainesville, Florida, USA
3 shared publicationsFei Zou
Department of Biostatistics University of Florida, Gainesville, Florida, USA
2 shared publicationsJan S. Moreb
Division of Hematology/Oncology, University of Florida, Gainesville, Florida, USA
2 shared publications- Rohit Bishnoi
Hematology and Oncology, University of Florida, Gainesville, USA
2 shared publications
Latest Publications
- 1 August 2019
- Published by Elsevier in The American Journal of Medicine
- Vol. 132 (8) , e658-e660
Reactive Perforating Collagenosis in End-Stage Renal Disease: Not All that Itches Is Uremic Pruritis!
- 1 August 2019
- Published by Elsevier in The American Journal of Medicine
- Vol. 132 (8) , e658-e660
Reactive Perforating Collagenosis in End-Stage Renal Disease: Not All that Itches Is Uremic Pruritis!
- 6 March 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (3) , e229059
Pauci-immune proliferative glomerulonephritis and fungal endocarditis: More than a mere coincidence?
Glomerulonephritis (GN) due to infective (primarily bacterial) endocarditis is well documented with the most common lesions being necrotising and crescentic GN, followed by endocapillary proliferative GN. Prominent C3 staining and subepithelial immune deposits on electron microscopy are commonly
- 6 March 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (3) , e229059
Pauci-immune proliferative glomerulonephritis and fungal endocarditis: More than a mere coincidence?
Glomerulonephritis (GN) due to infective (primarily bacterial) endocarditis is well documented with the most common lesions being necrotising and crescentic GN, followed by endocapillary proliferative GN. Prominent C3 staining and subepithelial immune deposits on electron microscopy are commonly
- 15 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2) , e229197
Liver transplant, toxoplasmosis and kidney stones: connecting the dots
A 62-year-old woman with a history of orthotopic liver transplantation for cirrhosis secondary to auto-immune hepatitis 3 months prior, presented with fever and new-onset seizures. Her maintenance immunosuppressive therapy included mycophenolate mofetil 500 mg twice a day, tacrolimus 1 mg
- 15 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2) , e229197
Liver transplant, toxoplasmosis and kidney stones: connecting the dots
A 62-year-old woman with a history of orthotopic liver transplantation for cirrhosis secondary to auto-immune hepatitis 3 months prior, presented with fever and new-onset seizures. Her maintenance immunosuppressive therapy included mycophenolate mofetil 500 mg twice a day, tacrolimus 1 mg
- 1 January 2019
- Published by Elsevier in The American Journal of Medicine
- Vol. 132 (1) , e9-e10
Keep an Eye on the Eye Symptoms of Your Dialysis Patient
- 1 January 2019
- Published by Elsevier in The American Journal of Medicine
- Vol. 132 (1) , e9-e10
Keep an Eye on the Eye Symptoms of Your Dialysis Patient
- 12 November 2018
- Published by Springer Nature in CEN Case Reports
- Vol. 8 (2) , 144-145
Calcific olecranon bursitis in end-stage renal disease
- 12 November 2018
- Published by Springer Nature in CEN Case Reports
- Vol. 8 (2) , 144-145
Calcific olecranon bursitis in end-stage renal disease
- Open Access
- 1 October 2018
- Published by Taylor & Francis in ClinicoEconomics and Outcomes Research
- Vol. ume 10, 611-618
The role of a best practice alert in the electronic medical record in reducing repetitive lab tests
Background: The recommendations of the American Board of Internal Medicine Foundation’s “Choosing Wisely®” initiative recognize the importance of improving the appropriateness of testing behavior and reducing the number of duplicate laboratory tests. Objective: To assess the effectiveness of an electronic medical record Best Practice Alert (BPA or “pop up”) intervention aimed at reducing duplicate laboratory tests and hospital costs. Design: Comparison of the number of duplicated laboratory tests performed on inpatients before and after the intervention. Setting: University of Florida Health Shands Hospital, Gainesville, FL, USA, during 2014–2017. Intervention: The electronic medical record intervention was a BPA pop-up alert that informed the ordering physician if a recent identical order already existed along with the “ordering time”, “collecting time”, “resulting time”, and the result itself. Main outcome measures: Percentage change in the number of inpatient duplicate orders of selected clinical biochemistry tests and cost savings from reduction of the duplicates. Student’s t-test and beta-binomial models were used to analyze the data. Results: Results from the beta-binomial model indicated that the intervention reduced the overall duplicates by 18% (OR=0.82, standard error=0.016, P-valueConclusions: The present study included all hospital inpatients and covered 17 clinical laboratory tests. This rather simple and low-cost intervention resulted in significant reductions in percentage duplicates of several tests and resulted in cost savings. The study also highlights the role of hospitalists in quality improvement.
- 1 October 2018
- Published by Taylor & Francis in ClinicoEconomics and Outcomes Research
- Vol. ume 10, 611-618
Open AccessThe role of a best practice alert in the electronic medical record in reducing repetitive lab tests
Background: The recommendations of the American Board of Internal Medicine Foundation’s “Choosing Wisely®” initiative recognize the importance of improving the appropriateness of testing behavior and reducing the number of duplicate laboratory tests. Objective: To assess the effectiveness of an electronic medical record Best Practice Alert (BPA or “pop up”) intervention aimed at reducing duplicate laboratory tests and hospital costs. Design: Comparison of the number of duplicated laboratory tests performed on inpatients before and after the intervention. Setting: University of Florida Health Shands Hospital, Gainesville, FL, USA, during 2014–2017. Intervention: The electronic medical record intervention was a BPA pop-up alert that informed the ordering physician if a recent identical order already existed along with the “ordering time”, “collecting time”, “resulting time”, and the result itself. Main outcome measures: Percentage change in the number of inpatient duplicate orders of selected clinical biochemistry tests and cost savings from reduction of the duplicates. Student’s t-test and beta-binomial models were used to analyze the data. Results: Results from the beta-binomial model indicated that the intervention reduced the overall duplicates by 18% (OR=0.82, standard error=0.016, P-valueConclusions: The present study included all hospital inpatients and covered 17 clinical laboratory tests. This rather simple and low-cost intervention resulted in significant reductions in percentage duplicates of several tests and resulted in cost savings. The study also highlights the role of hospitalists in quality improvement.
- Open Access
- 4 May 2018
- Published by Impact Journals, LLC in Oncotarget
- Vol. 9 (34) , 23704-23717
Efficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials
Efficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials Efficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials
- 4 May 2018
- Published by Impact Journals, LLC in Oncotarget
- Vol. 9 (34) , 23704-23717
Open AccessEfficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials
Efficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials Efficacy and safety of carfilzomib in relapsed and/or refractory multiple myeloma: systematic review and meta-analysis of 14 trials
- 21 February 2018
- Published by Taylor & Francis in Leukemia & Lymphoma
- Vol. 59 (11) , 2557-2569
Cardiotoxicity associated with carfilzomib: systematic review and meta-analysis
Carfilzomib is a second-generation proteasome inhibitor (PI) that is approved for patients with relapsed or refractory multiple myeloma (RRMM) who failed ≥1 prior lines of therapy. We performed a systematic review of carfilzomib literature with meta-analysis to determine cumulative incidence of cardiotoxicity. After the literature search, we included a total of 29 eligible phase I/II, phase II and phase III clinical trials which used carfilzomib. The cumulative incidence and overall odds ratios (OR) were calculated with random effect model, using ‘R’ software with metaphor package. A total of 4164 patients with various malignancies were included. The overall estimated cumulative incidence of cardiotoxicity was 8.68% and 4.92%, respectively, for all-grade and high-grade (≥ grade 3) toxicity, which seems higher than other PIs. Compared to control group, the odds of developing cardiotoxicity due to carfilzomib was significantly higher with OR of 2.03 (95% CI: 1.19–3.46, p = .010) and 2.04 (95% CI: 1.31–3.17, p = .002) for all-grades and high grades, respectively. Concomitant immunomodulatory agents seem to increase the risk of cardiotoxicity (high-grade cardiotoxicity 6.45% and 4.34% with and without concomitant immunomodulatory agents, respectively (p = .033)). There was no variation in the incidence of cardiotoxicity among newly diagnosed versus RRMM (p = .38), and high versus standard dose carfilzomib (p = .86).
- 21 February 2018
- Published by Taylor & Francis in Leukemia & Lymphoma
- Vol. 59 (11) , 2557-2569
Cardiotoxicity associated with carfilzomib: systematic review and meta-analysis
Carfilzomib is a second-generation proteasome inhibitor (PI) that is approved for patients with relapsed or refractory multiple myeloma (RRMM) who failed ≥1 prior lines of therapy. We performed a systematic review of carfilzomib literature with meta-analysis to determine cumulative incidence of cardiotoxicity. After the literature search, we included a total of 29 eligible phase I/II, phase II and phase III clinical trials which used carfilzomib. The cumulative incidence and overall odds ratios (OR) were calculated with random effect model, using ‘R’ software with metaphor package. A total of 4164 patients with various malignancies were included. The overall estimated cumulative incidence of cardiotoxicity was 8.68% and 4.92%, respectively, for all-grade and high-grade (≥ grade 3) toxicity, which seems higher than other PIs. Compared to control group, the odds of developing cardiotoxicity due to carfilzomib was significantly higher with OR of 2.03 (95% CI: 1.19–3.46, p = .010) and 2.04 (95% CI: 1.31–3.17, p = .002) for all-grades and high grades, respectively. Concomitant immunomodulatory agents seem to increase the risk of cardiotoxicity (high-grade cardiotoxicity 6.45% and 4.34% with and without concomitant immunomodulatory agents, respectively (p = .033)). There was no variation in the incidence of cardiotoxicity among newly diagnosed versus RRMM (p = .38), and high versus standard dose carfilzomib (p = .86).
- 1 October 2017
- Published by Elsevier in Journal of Thoracic Oncology
- Vol. 12 (10) , e169-e170
Novel Mutation Pair L858M/L861Q Caused Resistance to Both First- and Third-Generation EGFR Inhibitors, but Was Found to Be Sensitive to the Combination of Lapatinib and Erbitux
- 1 October 2017
- Published by Elsevier in Journal of Thoracic Oncology
- Vol. 12 (10) , e169-e170
Novel Mutation Pair L858M/L861Q Caused Resistance to Both First- and Third-Generation EGFR Inhibitors, but Was Found to Be Sensitive to the Combination of Lapatinib and Erbitux