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Therapeutic plasma exchange for neuromyelitis optica spectrum disorder: A multicenter retrospective study by the ASFA neurologic diseases subcommittee.
Ipe, Tina S; Raval, Jay S; Fernando, Leonor P; Gokhale, Amit; Jacquot, Cyril; Johnson, Andrew D; Kim, Haewon C; Monis, Grace F; Mo, Yunchun D; Morgan, Shanna M; Pagano, Monica B; Pham, Huy P; Sanford, Kimberly; Schmidt, Amy E; Schwartz, Joseph; Waldman, Amy; Webb, Jennifer; Winters, Jeffrey L; Wu, Yanyun; Yamada, Chisa; Wong, Edward C C.
Affiliation
  • Ipe TS; Department of Pathology and Laboratory Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Raval JS; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Fernando LP; Department of Pathology, University of New Mexico, Albuquerque, New Mexico.
  • Gokhale A; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina.
  • Jacquot C; Department of Pathology and Laboratory Medicine, University of California, Davis, Sacramento, California.
  • Johnson AD; Department of Pathology, Stony Brook University, Stony Brook, New York.
  • Kim HC; Department of Laboratory Medicine and Hematology, Children's National Health System, Washington, District of Columbia.
  • Monis GF; Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
  • Mo YD; Department of Pediatrics and Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Morgan SM; Department of Pathology and Laboratory Medicine, University of California, Davis, Sacramento, California.
  • Pagano MB; Department of Laboratory Medicine and Hematology, Children's National Health System, Washington, District of Columbia.
  • Pham HP; American Red Cross, Minneapolis, Minnesota.
  • Sanford K; Department of Laboratory Medicine, University of Washington, Seattle, Washington.
  • Schmidt AE; Department of Pathology, University of Southern California, Los Angeles, California.
  • Schwartz J; Department of Pathology, Virginia Commonwealth University, Richmond, Virginia.
  • Waldman A; Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.
  • Webb J; Department of Pathology and Cell Biology, Columbia University, New York, New York.
  • Winters JL; Department of Pediatrics and Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Wu Y; Department of Laboratory Medicine and Hematology, Children's National Health System, Washington, District of Columbia.
  • Yamada C; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
  • Wong ECC; Bloodworks Northwest, Seattle, Washington.
J Clin Apher ; 35(1): 25-32, 2020 Jan.
Article in En | MEDLINE | ID: mdl-31705563
ABSTRACT
IMPORTANCE Neuromyelitis optica/neuromyelitis optica spectrum disorder patients' response to therapeutic plasma exchange (TPE) is currently incompletely characterized.

OBJECTIVE:

Our study aims to understand the clinical status improvement of neuromyelitis optica/neuromyelitis optica spectrum disorder patients treated with TPE. DESIGN, SETTING, AND

PARTICIPANTS:

This is a multicenter retrospective study conducted between 1 January 2003 and 31 July 2017 at 13 US hospitals performing apheresis procedures. Subjects studied were diagnosed with neuromyelitis optica/neuromyelitis optica spectrum disorder who received TPE during presentation with acute disease. MAIN OUTCOMES AND

MEASURES:

The primary outcome was clinical status improvement in patients treated with TPE. Secondary measures were procedural and patient characteristics associated with response to treatment.

RESULTS:

We evaluated 114 patients from 13 institutions. There was a female predilection. The largest ethnic group affected was non-Hispanic Caucasian. The average age of diagnosis was 43.1 years. The average time to diagnosis was 3.1 years. On average, five procedures were performed during each treatment series. The most commonly performed plasma volume exchange was 1.0 to 1.25 using 5% albumin as replacement fluid. Most patients (52%) did not require an additional course of TPE and noted "mild" to "moderate" clinical status improvement. Maximal symptom improvement appeared by the fourth or fifth TPE treatment. CONCLUSION AND RELEVANCE TPE improved the clinical status of patients. Adults responded more favorably than children. Procedural characteristics, including number of TPEs, plasma volume exchanged, and replacement fluid used, were similar between institutions. TPE was well-tolerated and had a low severe adverse event profile.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Exchange / Neuromyelitis Optica Type of study: Observational_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Humans / Infant / Middle aged / Newborn Country/Region as subject: America do norte Language: En Journal: J Clin Apher Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Exchange / Neuromyelitis Optica Type of study: Observational_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Humans / Infant / Middle aged / Newborn Country/Region as subject: America do norte Language: En Journal: J Clin Apher Year: 2020 Type: Article