Literature DB >> 12368689

32P Radiosynoviorthesis in children with hemophilia.

Marilyn J Manco-Johnson1, Rachelle Nuss, James Lear, Jerome Wiedel, Susan J Geraghty, Michele R Hacker, Sharon Funk, Ray F Kilcoyne, James Murphy.   

Abstract

BACKGROUND: This study was performed to prospectively evaluate the safety, efficacy, and cost of injecting P-colloid into joints of children with hemophilia and synovitis to decrease the rate of joint bleeding. PATIENTS AND METHODS: Eligibility included a diagnosis of hemophilia, history of more than six hemorrhages into a joint within a 6-month period, and evidence of synovitis by objective imaging. With written, informed consent, 0.25 to 1.0 mCi of P-colloid was injected into the problem joints. Safety was monitored by external beta-scanning and physical assessment. Efficacy was determined by analysis of the change in joint hemorrhage frequency from 6 months before and up to 96 months after the injection using a signed-rank test. Physical assessment and pain assessment were analyzed similarly using values obtained within 1 week before and 6 months after the radiosynoviorthesis. Cost was modeled using charges from the authors' institution in relation to existing alternative therapies.
RESULTS: One hundred injections were given into 91 joints in 59 children. Seven children had high-titer neutralizing antibodies to factor VIII or IX. Nine children were infected with HIV. Joints injected included 44 ankles, 19 knees, 27 elbows, and 1 shoulder. Nine joints required reinjection. All children showed a significant decrease in bleeding rate (P < 0.0001) and pain (P = 0.03), with improved physical function (P = 0.02). In one child acute lymphocytic leukemia developed, but it was judged unrelated to the two P injections that he had received 3 and 10 months before the leukemia diagnosis. There were no cases of bleeding, infection, or inflammation caused by the injection. Cost was substantially less than medical and surgical alternatives.
CONCLUSIONS: Radiosynoviorthesis is effective in limiting the frequency of joint hemorrhage, decreasing pain and improving function in children with hemophilia. However, long-term safety studies are needed.

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Year:  2002        PMID: 12368689     DOI: 10.1097/00043426-200210000-00007

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  5 in total

1.  Musculoskeletal complications of hemophilia.

Authors:  E Carlos Rodriguez-Merchan
Journal:  HSS J       Date:  2009-11-17

2.  Intraarticular factor IX protein or gene replacement protects against development of hemophilic synovitis in the absence of circulating factor IX.

Authors:  Junjiang Sun; Narine Hakobyan; Leonard A Valentino; Brian L Feldman; R Jude Samulski; Paul E Monahan
Journal:  Blood       Date:  2008-08-20       Impact factor: 22.113

Review 3.  Haemophilia and joint disease: pathophysiology, evaluation, and management.

Authors:  Karin Knobe; Erik Berntorp
Journal:  J Comorb       Date:  2011-12-27

4.  Treatment with radiosynoviorthesis in hemophilic patients with and without inhibitor.

Authors:  Mario Edgar Tena-Sanabria; Yoriko Fabiola Rojas-Sato; José Carlos Castañeda-Resendiz; Gabriela Fuentes-Herrera; Félix Alejandro Álvarez-Martínez; Yureni Iraí Tena-Gonzalez; Juan Carlos Núñez-Enríquez
Journal:  BMC Pediatr       Date:  2020-04-20       Impact factor: 2.125

5.  The EANM guideline for radiosynoviorthesis.

Authors:  W U Kampen; B Boddenberg-Pätzold; M Fischer; M Gabriel; R Klett; M Konijnenberg; E Kresnik; H Lellouche; F Paycha; L Terslev; C Turkmen; F van der Zant; L Antunovic; E Panagiotidis; G Gnanasegaran; T Kuwert; T Van den Wyngaert
Journal:  Eur J Nucl Med Mol Imaging       Date:  2021-10-20       Impact factor: 9.236

  5 in total

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