Zhe (Amy) Wang
Research Subjects
Research Interests
Zhe (Amy) Wang has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Aleksandra Gelfman
Touro College of Pharmacy, New York, New York
1 shared publicationAlicia Bryan
Long Island University Pharmacy, Brooklyn, New York
1 shared publicationChristine Le
Touro College of Pharmacy, New York, New York
1 shared publication- Daniel R. Malcom
Sullivan University College of Pharmacy and Health Sciences, Louisville, Kentucky
1 shared publication Dean Gennaro
Long Island University Pharmacy, Brooklyn, New York
1 shared publicationDerek Marshall
Touro College of Pharmacy, New York, New York
1 shared publication
Latest Publications
- Open Access
- 23 April 2025
- Published by Elsevier in American Journal of Pharmaceutical Education
- Vol. 89 (5) , 101407
Perceptions of Service Workload Among United States Pharmacy Faculty and Administrators: A Focus Group Study
- 23 April 2025
- Published by Elsevier in American Journal of Pharmaceutical Education
- Vol. 89 (5) , 101407
Open AccessPerceptions of Service Workload Among United States Pharmacy Faculty and Administrators: A Focus Group Study
- Open Access
- 29 May 2023
- Published by MDPI AG in Preprints.org
Safety of Iron Chelation Therapies in Kidney Disease
Background: Iron chelation medications (desferoxamine, desferasirox, desferiprone) are used to manage iron overload. These medications are partially excreted via the kidneys, desferoxamine and desferiprone excretes primarily in the urine, and desferasirox had about 8% excreted in the urine. Their use in severe kidney disease and dialysis patients is caution as “avoided” concerning adverse effects; however, there are reports safe use. This manuscript reviews the literature in this population. Data Sources: Pubmed: desferasirox, deferiprone, deferoxamine, kidney disease, ESKD, Dialysis. Case reports and case series that described experiences with using iron chelation medications in ESKD patients are included. Data also gathered from reading-related sources. Results: This is a review of desferoxamine, desferasirox, and deferiprone use in kidney disease from 1976 to the present time. Table 1 provides a summary of findings. These are mostly reports and brief descriptions of the experiences used in severe kidney disease and dialysis, but lack of randomized control trials and small number of participants. Conclusions: Iron chelation medications are important for treating iron overload but concerns with adverse effects. Due to limited medications available to treat iron overload in patients with severe kidney disease, their safe use has been reporting in the literature. This is an area that warrants further research.
- 29 May 2023
- Published by MDPI AG in Preprints.org
Open AccessSafety of Iron Chelation Therapies in Kidney Disease
Background: Iron chelation medications (desferoxamine, desferasirox, desferiprone) are used to manage iron overload. These medications are partially excreted via the kidneys, desferoxamine and desferiprone excretes primarily in the urine, and desferasirox had about 8% excreted in the urine. Their use in severe kidney disease and dialysis patients is caution as “avoided” concerning adverse effects; however, there are reports safe use. This manuscript reviews the literature in this population. Data Sources: Pubmed: desferasirox, deferiprone, deferoxamine, kidney disease, ESKD, Dialysis. Case reports and case series that described experiences with using iron chelation medications in ESKD patients are included. Data also gathered from reading-related sources. Results: This is a review of desferoxamine, desferasirox, and deferiprone use in kidney disease from 1976 to the present time. Table 1 provides a summary of findings. These are mostly reports and brief descriptions of the experiences used in severe kidney disease and dialysis, but lack of randomized control trials and small number of participants. Conclusions: Iron chelation medications are important for treating iron overload but concerns with adverse effects. Due to limited medications available to treat iron overload in patients with severe kidney disease, their safe use has been reporting in the literature. This is an area that warrants further research.
- 28 November 2018
- Published by Hindawi Limited in Journal of Clinical Pharmacy and Therapeutics
- Vol. 44 (1) , 122-124
Lemierre's syndrome: One rare disease-Two case studies
What is known and objective Lemierre's syndrome is often misdiagnosed as a common cold or viral infection. Fusobacterium necrophorum is the most common causative organism. The recommended treatment regimen is 6 weeks of a beta‐lactam antibiotic along with metronidazole. Case description We present two cases of Lemierre's syndrome with internal jugular vein thrombophlebitis and positive blood cultures for F. necrophorum. The first case was successfully treated with 6 weeks of a beta‐lactam antibiotic and 4 weeks of metronidazole, while the second case was successfully treated with 4 weeks of a beta‐lactam antibiotic and 2 weeks of metronidazole. What is new and conclusion Two cases of Lemierre's syndrome were treated successfully with only 2‐4 weeks of metronidazole therapy. Shorter duration of metronidazole therapy should be explored in future studies.
- 28 November 2018
- Published by Hindawi Limited in Journal of Clinical Pharmacy and Therapeutics
- Vol. 44 (1) , 122-124
Lemierre's syndrome: One rare disease-Two case studies
What is known and objective Lemierre's syndrome is often misdiagnosed as a common cold or viral infection. Fusobacterium necrophorum is the most common causative organism. The recommended treatment regimen is 6 weeks of a beta‐lactam antibiotic along with metronidazole. Case description We present two cases of Lemierre's syndrome with internal jugular vein thrombophlebitis and positive blood cultures for F. necrophorum. The first case was successfully treated with 6 weeks of a beta‐lactam antibiotic and 4 weeks of metronidazole, while the second case was successfully treated with 4 weeks of a beta‐lactam antibiotic and 2 weeks of metronidazole. What is new and conclusion Two cases of Lemierre's syndrome were treated successfully with only 2‐4 weeks of metronidazole therapy. Shorter duration of metronidazole therapy should be explored in future studies.