Evidence map›Paper›PMID 34748552›Full record

ArticlePloS one2021

Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort.

Hong Si Nga, Lilian Monteiro Pereira Palma, Miguel Ernandes Neto, Ida Maria Maximina Fernandes-Charpiot, Valter Duro Garcia, Roger Kist, Silvana Maria Carvalho Miranda, Pedro Augusto Macedo de Souza, Gerson Marques Pereira, Luis Gustavo Modelli de Andrade

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Hong Si NgaDepartment of Internal Medicine-UNESP, Univ Estadual Paulista, Botucatu, Brazil.
Lilian Monteiro Pereira PalmaDepartamento de Pediatria/Hospital de Clínicas, Universidade Estadual de Campinas, Campinas, SP, Brazil.
Miguel Ernandes NetoDepartment of Internal Medicine-UNESP, Univ Estadual Paulista, Botucatu, Brazil.
Ida Maria Maximina Fernandes-CharpiotTransplant Unit São Jose Rio Preto/FAMERP, Sao Paulo, Brazil.
Valter Duro GarciaTransplant Unit Santa Casa de Misericórdia de Porto Alegre-ISCMPA, Porto Alegre, Brazil.ORCID 0000-0002-7394-1501
Roger KistTransplant Unit Santa Casa de Misericórdia de Porto Alegre-ISCMPA, Porto Alegre, Brazil.ORCID 0000-0001-7338-2431
Silvana Maria Carvalho MirandaSanta Casa de Belo Horizonte, Belo Horizonte, Brazil.
Pedro Augusto Macedo de SouzaSanta Casa de Belo Horizonte, Belo Horizonte, Brazil.ORCID 0000-0001-5436-3956
Gerson Marques PereiraSanta Casa de Belo Horizonte, Belo Horizonte, Brazil.
Luis Gustavo Modelli de AndradeDepartment of Internal Medicine-UNESP, Univ Estadual Paulista, Botucatu, Brazil.ORCID 0000-0002-0230-0766
Grupo Santa Casa de Belo Horizonte · BRUniversidade Estadual Paulista (Unesp) · BRSanta Casa de Misericórdia de Marília · BRFaculdade de Medicina de São José do Rio Preto · BRUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtypical Hemolytic Uremic Syndrome (aHUS) is an ultra-rare disease that potentially leads to kidney graft failure due to ongoing Thrombotic Microangiopathy (TMA). The aim was evaluating the frequency of TMA after kidney transplantation in patients with aHUS in a Brazilian cohort stratified by the use of the specific complement-inhibitor eculizumab.

methodsThis was a multicenter retrospective cohort study including kidney transplant patients diagnosed with aHUS. We collected data from 118 transplant centers in Brazil concerning aHUS transplanted patients between 01/01/2007 and 12/31/2019. Patients were stratified into three groups: no use of eculizumab (No Eculizumab Group), use of eculizumab for treatment of after transplantation TMA (Therapeutic Group), and use of eculizumab for prophylaxis of aHUS recurrence (Prophylactic Group).

resultsThirty-eight patients with aHUS who received kidney transplantation were enrolled in the study. Patients' mean age was 30 years (24-40), and the majority of participants was women (63% of cases). In the No Eculizumab Group (n = 11), there was a 91% graft loss due to the TMA. The hazard ratio of TMA graft loss was 0.07 [0.01-0.55], p = 0.012 in the eculizumab Prophylactic Group and 0.04 [0.00-0.28], p = 0.002 in the eculizumab Therapeutic Group.

conclusionThe TMA graft loss in the absence of a specific complement-inhibitor was higher among the Brazilian cohort of kidney transplant patients. This finding reinforces the need of eculizumab use for treatment of aHUS kidney transplant patients. Cost optimization analysis and the early access to C5 inhibitors are suggested, especially in low-medium income countries.

Indexed as

AdultAntibodies, Monoclonal, HumanizedAtypical Hemolytic Uremic SyndromeBrazilComplement Inactivating AgentsFemaleGraft RejectionHumansKidney TransplantationMaleRetrospective StudiesThrombotic MicroangiopathiesYoung AdultAntibodies, Monoclonal, HumanizedComplement Inactivating Agentseculizumab

Identifiers

PMID34748552
PMCPMC8575299
OpenAlexW3212793120

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.