Literature DB >> 29737462

Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy.

Giovanni Luca Tiscia1, Angelo Ostuni2, Nicola Cascavilla1, Filomena Cappucci1, Potito Scalzulli1, Cosima Battista2, Antonio Abrescia3, Filippo Aucella1, Caterina Buquicchio3, Maurizio Brigante4, Giovanna D'Andrea5, Bruno Di Paolo6, Giulio Giordano4, Barbara Infante5, Silvia Piano4, Prudenza Ranieri2, Livio Tullo4, Elvira Grandone7.   

Abstract

Severe ADAMTS13 deficiency (activity < 10%) is pathognomonic of thrombotic thrombocytopenic purpura. ADAMTS13 testing is time-consuming and unavailable in many hospitals. Recently, a seven-variables score named PLASMIC score, has been developed to stratify acute patients, based on their risk of having a severe ADAMTS13 deficiency. We present the application of this score in a cohort of patients referred to our Center. From 2012 to 2017, 42 patients with suspected thrombotic microangiopathies from 6 Centers were referred to Hemostasis and Thrombosis Center of "Casa Sollievo della Sofferenza" Hospital/Research Institute for ADAMTS13 testing. For all patients, relevant medical and laboratory information were collected. To obtain the statistical measure of the discriminatory power of PLASMIC scoring system, the Area Under the Curve Receiver Operating Characteristic (AUC ROC) was calculated. We were able to calculate the PLASMIC score in 27 out of 42 patients; we found a good discrimination performance of the score with a resulting AUC value of 0.86 (95% CI 0.71-1.0; p = 0.015). All patients but one with a high risk PLASMIC score (6-7) showed a severe deficiency. Among patients belonging to the intermediate risk (PLASMIC score 5) group, 2 showed normal ADAMTS13 activity and 2 levels below 10%. In none of the patients in the low risk group (PLASMIC score 0-4), a severe ADAMTS13 deficiency was found. Present results confirm and extend previous data regarding the predictive value of the PLASMIC score. Indeed, it shows a good diagnostic performance and can be useful for decision makers to properly and promptly define the better therapeutic approach.

Entities:  

Keywords:  ADAMTS13; Plasmapheresis; Thrombotic microangiopathies; Thrombotic thrombocytopenic purpura

Mesh:

Substances:

Year:  2018        PMID: 29737462     DOI: 10.1007/s11239-018-1674-6

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  21 in total

Review 1.  Thrombotic microangiopathies.

Authors:  Joel L Moake
Journal:  N Engl J Med       Date:  2002-08-22       Impact factor: 91.245

2.  ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor.

Authors:  Jing-fei Dong; Joel L Moake; Aubrey Bernardo; Kazuo Fujikawa; Chalmette Ball; Leticia Nolasco; José A López; Miguel A Cruz
Journal:  J Biol Chem       Date:  2003-05-29       Impact factor: 5.157

Review 3.  Cleavage of ultra-large von Willebrand factor by ADAMTS-13 under flow conditions.

Authors:  J-F Dong
Journal:  J Thromb Haemost       Date:  2005-08       Impact factor: 5.824

4.  Survival and relapse in patients with thrombotic thrombocytopenic purpura.

Authors:  Johanna A Kremer Hovinga; Sara K Vesely; Deirdra R Terrell; Bernhard Lämmle; James N George
Journal:  Blood       Date:  2009-12-23       Impact factor: 22.113

5.  Validation of the PLASMIC score at a University Medical Center.

Authors:  Ryan Jajosky; Mark Floyd; Thomas Thompson; James Shikle
Journal:  Transfus Apher Sci       Date:  2017-07-08       Impact factor: 1.764

6.  Derivation and external validation of the PLASMIC score for rapid assessment of adults with thrombotic microangiopathies: a cohort study.

Authors:  Pavan K Bendapudi; Shelley Hurwitz; Ashley Fry; Marisa B Marques; Stephen W Waldo; Ang Li; Lova Sun; Vivek Upadhyay; Ayad Hamdan; Andrew M Brunner; John M Gansner; Srinivas Viswanathan; Richard M Kaufman; Lynne Uhl; Christopher P Stowell; Walter H Dzik; Robert S Makar
Journal:  Lancet Haematol       Date:  2017-03-02       Impact factor: 18.959

7.  Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13).

Authors:  A Tripodi; F Peyvandi; V Chantarangkul; R Palla; A Afrasiabi; M T Canciani; D W Chung; S Ferrari; Y Fujimura; M Karimi; K Kokame; J A Kremer Hovinga; B Lämmle; S F de Meyer; B Plaimauer; K Vanhoorelbeke; K Varadi; P M Mannucci
Journal:  J Thromb Haemost       Date:  2008-07-26       Impact factor: 5.824

8.  Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation.

Authors:  J L Moake; N A Turner; N A Stathopoulos; L H Nolasco; J D Hellums
Journal:  J Clin Invest       Date:  1986-12       Impact factor: 14.808

9.  Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome.

Authors:  C M Legendre; C Licht; P Muus; L A Greenbaum; S Babu; C Bedrosian; C Bingham; D J Cohen; Y Delmas; K Douglas; F Eitner; T Feldkamp; D Fouque; R R Furman; O Gaber; M Herthelius; M Hourmant; D Karpman; Y Lebranchu; C Mariat; J Menne; B Moulin; J Nürnberger; M Ogawa; G Remuzzi; T Richard; R Sberro-Soussan; B Severino; N S Sheerin; A Trivelli; L B Zimmerhackl; T Goodship; C Loirat
Journal:  N Engl J Med       Date:  2013-06-06       Impact factor: 91.245

10.  Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion.

Authors:  H M Tsai
Journal:  Blood       Date:  1996-05-15       Impact factor: 22.113

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  5 in total

1.  Application of PLASMIC Score in Risk Prediction of Thrombotic Thrombocytopenic Purpura: Real-World Experience From a Tertiary Medical Center in Taiwan.

Authors:  Chun-Hui Lee; Yi-Ching Huang; Sin-Syue Li; Ya-Ting Hsu; Ya-Ping Chen; Tsai-Yun Chen
Journal:  Front Med (Lausanne)       Date:  2022-05-09

2.  Comparison of Clinical Scoring Systems in the Management of Patients with Microangiopathic Hemolytic Anemia and Thrombocytopenia

Authors:  Mehmet Baysal; Elif Ümit; Hakkı Onur Kırkızlar; Ahmet Muzaffer Demir
Journal:  Turk J Haematol       Date:  2020-11-09       Impact factor: 1.831

3.  Focus on Key Issues in Immune Thrombotic Thrombocytopenic Purpura: Italian Experience of Six Centers.

Authors:  Giovanni Tiscia; Maria Teresa Sartori; Gaetano Giuffrida; Angelo Ostuni; Nicola Cascavilla; Daniela Nicolosi; Cosima Battista; Teresa Maria Santeramo; Lorella Melillo; Giulio Giordano; Filomena Cappucci; Lucia Fischetti; Elena Chinni; Giuseppe Tarantini; Anna Cerbo; Antonella Bertomoro; Fabrizio Fabris; Elvira Grandone
Journal:  J Clin Med       Date:  2021-12-04       Impact factor: 4.241

4.  Proteinuria Increases the PLASMIC and French Scores Performance to Predict Thrombotic Thrombocytopenic Purpura in Patients With Thrombotic Microangiopathy Syndrome.

Authors:  Nicolas Fage; Corentin Orvain; Nicolas Henry; Chloé Mellaza; François Beloncle; Marie Tuffigo; Franck Geneviève; Paul Coppo; Jean François Augusto; Benoit Brilland
Journal:  Kidney Int Rep       Date:  2021-11-16

5.  Obstetric outcomes in pregnant COVID-19 women: the imbalance of von Willebrand factor and ADAMTS13 axis.

Authors:  Elvira Grandone; Antonella Vimercati; Felice Sorrentino; Donatella Colaizzo; Angelo Ostuni; Oronzo Ceci; Manuela Capozza; Giovanni Tiscia; Antonio De Laurenzo; Mario Mastroianno; Filomena Cappucci; Lucia Fischetti; Maurizio Margaglione; Ettore Cicinelli; Luigi Nappi
Journal:  BMC Pregnancy Childbirth       Date:  2022-02-21       Impact factor: 3.007

  5 in total

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