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Mann, Steven A.

https://orcid.org/0000-0002-8163-1423

Mayo Clinic

University of Alabama at Birmingham

Citations 2

Use of hydroxyethyl starch in leukocytapheresis procedures does not increase renal toxicity
Harmon, Charles S., Cooling, Laura , Connelly‐Smith, Laura , Mann, Steven A. , Pham, Huy P. , Marques, Marisa B. , Schlueter, Annette J. , Case, Rosemary, King, Karen E., Cataife, Guido, Wu, Yanyun , Wong, Edward C.C. , Winters, Jeffrey L , Pagano, Monica B. , Winters, Jeffrey L. , Pham, Huy P , Schlueter, Annette J , Marques, Marisa B

Transfusion | September 7, 2016 | Volume: 56 | Issue: 11 | Pages: 2848-2856

10.1111/trf.13795 Get It

BACKGROUNDHydroxyethyl starch (HES) is reportedly associated with an increased risk of renal failure and death when used for fluid resuscitation in critically ill patients. HES can be used during therapeutic leukocytapheresis (TL) procedures to enhance cell separation. The purpose of this study was to evaluate the occurrence of adverse events associated with HES during TL procedures.STUDY DESIGN AND METHODSWe performed a retrospective review of patients who underwent TL with and without HES in the period 2009 to 2013 at six academic medical institutions.RESULTSA difference‐in‐difference regression analysis was used to estimate the mean change before and after TL in selected outcomes in the HES group relative to the average change in the non‐HES group. Selected outcomes included serum creatinine, estimated glomerular filtration rate (eGFR), and white blood cell (WBC) count. A total of 195 patients who underwent 278 TL procedures were studied. We found no significant differences in serum creatinine levels and eGFR on Days 1 and 7 after TL procedure between patients who received and those who did not receive HES. The rate of adverse events and overall and early mortality were similar in both groups. Patients with acute myeloid leukemia who received HES had greater WBC reduction when HES was used. Additionally, patients who received HES had improvement in pulmonary leukostasis symptoms.CONCLUSIONHES, used at low doses during TL procedures, was not associated with adverse events previously ascribed to its use as a volume expander.
Establishing an institutional therapeutic apheresis registry
Mann, Steven A. , McCleskey, Brandi , Marques, Marisa B. , Adamski, Jill , Marques, Marisa B

Journal of Clinical Apheresis | January 23, 2016 | Volume: 31 | Issue: 6 | Pages: 516-522

10.1002/jca.21443 Get It

Apheresis was first performed as a therapeutic procedure in the 1950s. The first national therapeutic apheresis (TA) registry was established in Canada in 1981 and other national registries followed, including two attempts at establishing an international TA registry. There is no national registry in the United States. Our large, academic, tertiary hospital has a very active TA service. We created a TA database to track all procedures performed by the apheresis service by transferring data from paper appointment logs and the electronic medical records into a Microsoft Access database. Retrospective data from each TA procedure performed at UAB from January 1, 2003 through December 31, 2012 were entered, including the type of procedure, indication, date, and patient demographics. Microsoft Excel was used for data analysis. During the 10‐year period, our TA service treated 1,060 patients and performed 11,718 procedures. Of these patients, 70% received therapeutic plasma exchange (TPE), 21% received extracorporeal photopheresis (ECP), 4.5% received red cell exchange (RCE), 4.2% received leukocytapheresis, and 0.6% underwent platelet depletion. Among the procedures, 54% were TPEs, 44% were ECPs, 1.3% were RCEs, 0.5% were leukocytaphereses, and 0.1% were platelet depletions. According to the current literature, national and international TA use is underreported. We believe that the UAB TA registry provides useful information about TA practices in our region and can serve as a model for other institutions. Furthermore, data from multiple institutional registries can be used for clinical research to increase the available evidence for the role of TA in various conditions. J. Clin. Apheresis 31:516–522, 2016. © 2015 Wiley Periodicals, Inc.