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Your search keyword '"Nusrat, Sanober"' showing total 24 results
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24 results on '"Nusrat, Sanober"'

2. PROMISE: a real-world clinical-genomic database to address knowledge gaps in prostate cancer

Author

Koshkin, Vadim S., Patel, Vaibhav G., Ali, Alicia, Bilen, Mehmet A., Ravindranathan, Deepak, Park, Joseph J., Kellezi, Olesia, Cieslik, Marcin, Shaya, Justin, Cabal, Angelo, Brown, Landon, Labriola, Matthew, Graham, Laura S., Pritchard, Colin, Tripathi, Abhishek, Nusrat, Sanober, Barata, Pedro, Jang, Albert, Chen, Shuang R., Garje, Rohan, Acharya, Luna, Hwang, Clara, Pilling, Amanda, Oh, William, Jun, Tomi, Natesan, Divya, Nguyen, Chris, Kilari, Deepak, Pierro, Michael, Thapa, Bicky, Cackowski, Frank, Mack, Alleda, Heath, Elisabeth, Marshall, Catherine H., Tagawa, Scott T., Halabi, Susan, Schweizer, Michael T., Armstrong, Andrew, Dorff, Tanya, Alva, Ajjai, and McKay, Rana

Published
2022
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3. Thrombotic Microangiopathy After Hematopoietic Stem Cell and Solid Organ Transplantation: A Review for Intensive Care Physicians.

Author

Nusrat, Sanober, Davis, Hugh, MacDougall, Kira, George, James N., Nakamura, Ryotaro, and Borogovac, Azra

Subjects
*HEMATOPOIETIC stem cells, *INTENSIVE care units, *PRIMARY health care, *THROMBOTIC microangiopathies, *RITUXIMAB, *TRANSPLANTATION of organs, tissues, etc.
Abstract

Intensive care physicians may assume the primary care of patients with transplant-associated thrombotic microangiopathy (TA-TMA), an uncommon but potentially critical complication of hematopoietic stem cell transplants (HSCTs) and solid organ transplants. TA-TMA can have a dramatic presentation with multiple organ dysfunction syndrome (MODS) associated with high morbidity and mortality. The typical presenting clinical features are hemolytic anemia, thrombocytopenia, refractory hypertension, proteinuria and worsening renal failure. Intestinal involvement, with abdominal pain, nausea and vomiting, gastrointestinal bleeding, and ascites are also common. Cardiopulmonary involvement may develop from various causes including pulmonary arteriolar hypertension, pleural and pericardial effusions, and diffuse alveolar hemorrhage. Due to other often concurrent complications after HSCT, early diagnosis and effective management of TA-TMA may be challenging. Close collaboration between ICU and transplant physicians, along with other relevant specialists, is needed to best manage these patients. There are currently no approved therapies for the treatment of TA-TMA. Plasma exchange and rituximab are not recommended unless circulating factor H (CFH) antibodies or thrombotic thrombocytopenic purpura (TTP; ADAMTS activity < 10%) are diagnosed or highly suspected. The role of the complement pathway activation in the pathophysiology of TA-TMA has led to the successful use of targeted complement inhibitors, such as eculizumab. However, the relatively larger studies using eculizumab have been mostly conducted in the pediatric population with limited data on the adult population. This review is focused on the role of intensive care physicians to emphasize the clinical approach to patients with suspected TA-TMA and to discuss diagnosis and treatment strategies. [ABSTRACT FROM AUTHOR]

Published
2024
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11. PROMISE: a real-world clinical-genomic database to address knowledge gaps in prostate cancer

Author

Koshkin, Vadim S., primary, Patel, Vaibhav G., additional, Ali, Alicia, additional, Bilen, Mehmet A., additional, Ravindranathan, Deepak, additional, Park, Joseph J., additional, Kellezi, Olesia, additional, Cieslik, Marcin, additional, Shaya, Justin, additional, Cabal, Angelo, additional, Brown, Landon, additional, Labriola, Matthew, additional, Graham, Laura S., additional, Pritchard, Colin, additional, Tripathi, Abhishek, additional, Nusrat, Sanober, additional, Barata, Pedro, additional, Jang, Albert, additional, Chen, Shuang R., additional, Garje, Rohan, additional, Acharya, Luna, additional, Hwang, Clara, additional, Pilling, Amanda, additional, Oh, William, additional, Jun, Tomi, additional, Natesan, Divya, additional, Nguyen, Chris, additional, Kilari, Deepak, additional, Pierro, Michael, additional, Thapa, Bicky, additional, Cackowski, Frank, additional, Mack, Alleda, additional, Heath, Elisabeth, additional, Marshall, Catherine H., additional, Tagawa, Scott T., additional, Halabi, Susan, additional, Schweizer, Michael T., additional, Armstrong, Andrew, additional, Dorff, Tanya, additional, Alva, Ajjai, additional, and McKay, Rana, additional

Published
2021
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15. A Rare Presentation of Neutrophilic Eccrine Hidradenitis in the Management of Acute Myeloid Leukaemia: A Case Report

Author

Sai Sridhar Boddupalli, Syed Talal, Nusrat Sanober, Jennifer Holter, Shannie Frisbie, Susanna Varkey Ulahannan, Midhun Malla, and Adam S. Asch

Subjects
Cancer Research, medicine.medical_specialty, Oncology, business.industry, Neutrophilic eccrine hidradenitis, medicine, Presentation (obstetrics), Myeloid leukaemia, medicine.disease, business, Dermatology
Published
2018

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