ABSTRACT
The recurrence of thrombotic thrombocytopenic purpura (TTP) in 20 to 50% of patients
who survive their initial episode, is not only a challenge to manage clinically, but
brings to light our lack of understanding of the underlying pathophysiology. Recurrence
may occur close to apparent hematologic remission or remotely, months later. Given
that surveillance of TTP relies on surrogate measures such as hematologic recovery,
normalization of serum lactate dehydrogenase (LDH) and resolution of clinical signs,
it is plausible that some recurrences are actually a continuum of disease. Standardizing
definitions for remission, exacerbation, and relapse are important for consistency
of patient management and interpreting the medical literature. When TTP recurs, several
adjuncts to therapeutic plasma exchange (TPE) have been used, including splenectomy,
vincristine, and rituximab. Although it would seem intuitive that more severe disease
would predict a greater likelihood of relapse, the degree of thrombocytopenia at presentation,
the persistence of schistocytosis at discontinuation of TPE, the elevation of LDH,
and the length of time to attain clinical remission are not reliable indicators of
the clinical outcome of any individual TTP patient. Measurement of ADAMTS13 activity
and its inhibitor offer new promise for prognostic and pathophysiologic significance;
however, more extensive scientific investigation is needed.
KEYWORDS
Thrombotic thrombocytopenic purpura (TTP) - prognostic factors - relapse - adjunct
therapy
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Nicholas BandarenkoM.D.
University of North Carolina Hospitals, Transfusion Medicine Service
1021 East Wing Campus Box #7600, 101 Manning Drive, Chapel Hill, NC 27514
Email: nbandare@unch.unc.edu