Evidence map›Paper›PMID 33325084›Full record

Observational studyJournal of clinical apheresis2021

Direct hemoperfusion using a polymyxin B-immobilized polystyrene column for COVID-19.

Daisuke Katagiri, Masahiro Ishikane, Yusuke Asai, Shinyu Izumi, Jin Takasaki, Hiyori Katsuoka, Isao Kondo, Satoshi Ide, Keiji Nakamura, Takato Nakamoto and 22 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of clinical apheresis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Establishment and clinical application of SARS-CoV-2 catch column.Clinical and experimental nephrology · 2023
    Article
  8. Review
  9. Article
  10. Review
  11. Apheresis and COVID-19 in intensive care unit (ICU).Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. When should polymyxin B-immobilized polystyrene column be introduced to improve COVID-19 prognosis?Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy · 2022
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

32 authors at 1 institution in 1 country.

Daisuke KatagiriDepartment of Nephrology, National Center for Global Health and Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1395-2644
Masahiro IshikaneDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Yusuke AsaiAntimicrobial Resistance Clinical Reference Center, Disease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Shinyu IzumiDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Jin TakasakiDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Hiyori KatsuokaMedical Equipment Management Office, National Center for Global Health and Medicine, Tokyo, Japan.
Isao KondoDepartment of Nephrology, National Center for Global Health and Medicine, Tokyo, Japan.
Satoshi IdeDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Keiji NakamuraDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Takato NakamotoDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Hidetoshi NomotoDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Yutaro AkiyamaDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Yusuke MiyazatoDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Tetsuya SuzukiDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Noriko KinoshitaDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Tatsunori OgawaMedical Equipment Management Office, National Center for Global Health and Medicine, Tokyo, Japan.
Tomiteru ToganoDepartment of Hematology, National Center for Global Health and Medicine, Tokyo, Japan.
Manabu SuzukiDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Masao HashimotoDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Keita SakamotoDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Yusaku KusabaDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Takashi KatsunoDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Takashi FukayaMedical Equipment Management Office, National Center for Global Health and Medicine, Tokyo, Japan.
Masayuki HojoDepartment of Respiratory Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Masaya SugiyamaGenome Medical Sciences Project, Research Institute, National Center for Global Health and Medicine, Ichikawa, Japan.
Masashi MizokamiGenome Medical Sciences Project, Research Institute, National Center for Global Health and Medicine, Ichikawa, Japan.
Tatsuya OkamotoDepartment of Intensive Care Medicine, National Center for Global Health and Medicine, Tokyo, Japan.
Akio KimuraDepartment of Emergency Medicine and Critical Care, National Center for Global Health and Medicine, Tokyo, Japan.
Eisei NoiriNational Center Biobank Network, National Center for Global Health and Medicine, Tokyo, Japan.
Norio OhmagariDisease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Fumihiko HinoshitaDepartment of Nephrology, National Center for Global Health and Medicine, Tokyo, Japan.
Haruhito SugiyamaNational Center Biobank Network, National Center for Global Health and Medicine, Tokyo, Japan.
National Center for Global Health and Medicine · JP

Funding

Grants-in-Aid for Research from the National Center for Global Health and Medicine 20A-3002Japan Agency for Medical Research and Development 20he0822003j0001
6 · The paper itself

Abstract

objectiveTo evaluate the efficacy and safety of direct hemoperfusion using a polymyxin B-immobilized polystyrene column (PMX-DHP) in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-positive pneumonia patients.

methodsThis study was a case series conducted at a designated infectious diseases hospital. Twelve SARS-CoV-2-positive patients with partial pressure of arterial oxygen/percentage of inspired oxygen (P/F) ratio < 300 were treated with PMX-DHP on two consecutive days each during hospitalization. We defined day 1 as the first day when PMX-DHP was performed. PMX-DHP efficacy was assessed on days 7 and 14 after the first treatment based on eight categories. Subsequently, improvement in P/F ratio and urinary biomarkers on days 4 and 8, malfunctions, and ventilator and extracorporeal membrane oxygenation avoidance rates were also evaluated.

resultsOn day 14 after the first treatment, disease severity decreased in 58.3% of the patients. P/F ratio increased while urine β2-microglobulin decreased on days 4 and 8. Cytokine measurement pre- and post-PMX-DHP revealed decreased levels of interleukin-6 and the factors involved in vascular endothelial injury, including vascular endothelial growth factor. Twenty-two PMX-DHPs were performed, of which seven and five PMX-DHPs led to increased inlet pressure and membrane coagulation, respectively. When the membranes coagulated, the circuitry needed to be reconfigured. Circuit problems were usually observed when D-dimer and fibrin degradation product levels were high before PMX-DHP.

conclusionsFuture studies are expected to determine the therapeutic effect of PMX-DHP on COVID-19. Because of the relatively high risk of circuit coagulation, coagulation capacity should be assessed beforehand.

Indexed as

AdultAgedAged, 80 and overArteriesbeta 2-MicroglobulinBiomarkersBlood Gas AnalysisCOVID-19CytokinesEndothelium, VascularFemaleHemoperfusionHospitalizationHumansMaleMiddle Agedbeta 2-MicroglobulinBiomarkersCytokinesOxygenPolymyxin BPolystyrenescytokinepneumoniasteroids

Identifiers

PMID33325084
PMCPMC8246724
OpenAlexW3112860025

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.