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Enregistrement W2954346506 · doi:10.1182/blood.v128.22.1366.1366

Diagnosis and Outcomes of Patients Presenting with Microangiopathic Hemolytic Anemia and Thrombocytopenia to a University Hospital Apheresis Unit

2016· article· en· W2954346506 sur OpenAlexaffabout
Katerina Pavenski, Megan Buchholz, Michelle Sholzberg

Notice bibliographique

RevueBlood · 2016
Typearticle
Langueen
DomaineImmunology and Microbiology
ThématiqueComplement system in diseases
Établissements canadiensUniversity of TorontoSt. Michael's Hospital
Organismes subventionnairesnon disponible
Mots-clésMedicineMicroangiopathic hemolytic anemiaADAMTS13EtiologyApheresisThrombotic thrombocytopenic purpuraPediatricsInternal medicineThrombotic microangiopathyEculizumabComplement systemDiseaseImmune systemImmunologyPlatelet

Résumé

récupéré en direct d'OpenAlex

Abstract Background: A syndrome of MAHA, thrombocytopenia and microthrombosis (MAHATT) can result from a variety of etiologies. Making an accurate diagnosis is important to guide treatment decisions and to inform prognosis. Our centre is one of the two adult apheresis centres serving a catchment area of over 5 million people. Our centre maintains database of all patients who were referred for investigation and treatment of MAHATT. Materials and Methods: ADAMTS13 testing was performed at our centre by a qualitative collagen binding assay before 2011 and by ELISA (Technoclone GmbH, Viennna) after 2011. Complement genetics studies included screening CFI, CFH, CFB, CD46/MCP, CFHR5, C3, APLN and THBD genes and were performed at the Hospital for Sick Children, Toronto. Complement protein and function studies were performed at the laboratories of the University of Heidelberg, Heidelberg and St. Justine Hospital, Montreal. Results: Between January 1 2010 and December 31 2015, 78 patients were referred with a presumed diagnosis of TTP for apheresis. On presentation, all patients had evidence of MAHA, thrombocytopenia and organ involvement. Five additional patients had a history of MAHATT and were referred for a second opinion. 2 patients did not have ADAMTS13 done and died during admission. The remaining 81 patients could be divided into 4 groups. Group 1 (TTP). 34 patients were found to have severe ADAMTS13 deficiency (activity less than 5%) and were diagnosed with TTP. Three additional patients were included in this Group despite having ADAMTS13>5% on presentation: one with relapse of immune TTP and two with known hereditary TTP. All were treated with apheresis. Only one patient required IHD (3%) and 36/37 (97%) survived to discharge. Group 2 (definite secondary thrombotic microangiopathy). 15 patients had been given alternative diagnoses: cancer 5, STEC-HUS 4, scleroderma 3, drug-associated TMA 2 and hemaphagocytic syndrome 1. 6/15 (40%) required dialysis and 9/15 (60%) survived to discharge. Group 3 (possible secondary thrombotic microangiopathy). In 16 patients, MAHATT was associated with other risk factors including autoimmune disease 5, acute pancreatitis 3, malignant hypertension 3, postpartum state 2, post-splenectomy 1, post-alloBMT/sepsis 1, and dyskeratosis congenita/post-alloBMT 1. 11 patients had complement genetics screen and in 10 cases the results were normal. 7/16 (44%) required dialysis and all patients survived to discharge. Group 4 (complement-mediated HUS). 13 patients were diagnosed with cm-HUS. All patients had MAHATT and acute kidney injury. 11/13 had complement genetics screen and in 7/11 the results were normal. 5 patients underwent anti-CFH antibody testing; 2 patients had detectable anti-CFH antibodies. Both of these patients had normal genetics screen. Thus, in 6/11 (55%) patients a complement abnormality has been identified on diagnostic testing. 8/13 (62%) required hemodialysis and all patients survived to discharge. Of note, 4/83 patients had SLE. TMA was attributed to immune TTP (2 cases), lupus flare/vasculitis (1) and cm-HUS due to anti-CFH antibody (1). In these patients SLE was diagnosed from 13 years earlier to 4 years after presentation with MAHATT. Conclusions: TTP accounted for the majority of patients referred with MAHATT to our centre and was generally associated with excellent short-term outcomes. The worst mortality was observed in patients with definite secondary TMA (40%) and dialysis requirement was highest in the cm-HUS group (62%). Anti-CFH antibody testing and complement genetics screen was positive in about 50% of patients diagnosed with cm-HUS. SLE in patients with MAHATT is not common (5%) and may result from different pathogenic processes. Timely diagnosis and appropriate management are imperative to minimizing morbidity and mortality in this vulnerable patient population. Disclosures Pavenski: Alexion Pharmaceuticals Inc.: Honoraria, Other: attended an entity's advisory boards. Sholzberg:Shire (previously Baxter, Baxalta): Honoraria, Research Funding; Novonordisk: Honoraria.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: Observationnel
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,015
Score d'incertitude au seuil0,309

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0000,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,009
Tête enseignante GPT0,207
Écart entre enseignants0,198 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2016
Routes d'admission2
Résumé présentoui

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