Evidence map›Paper›PMID 31296835›Full record

ArticleAnnals of transplantation2019

Infectious Complications of Induction Therapies in Kidney Transplantation.

Adem Bayraktar, Yunus Catma, Arif Akyildiz, Erol Demir, Huseyin Bakkaloglu, Ali Riza Ucar, Ahmet Burak Dirim, Sebahat Usta Akgul, Sonay Temurhan, Ali Fuat Kaan Gok and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of transplantation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 23 citations in OpenAlex.

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  4. Acta medica Lituanic · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Adem BayraktarDepartment of General Surgery, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Yunus CatmaDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Arif AkyildizDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Erol DemirDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Huseyin BakkalogluDepartment of General Surgery, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Ali Riza UcarDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Ahmet Burak DirimDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Sebahat Usta AkgulDepartment of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Sonay TemurhanDepartment of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Ali Fuat Kaan GokDepartment of General Surgery, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Yasemin OzlukDepartment of Pathology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Isin KilicaslanDepartment of Pathology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Fatma Savran OguzDepartment of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Mehmet Sukru SeverDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Ali Emin AydinDepartment of General Surgery, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Aydin TurkmenDivision of Nephrology, Department of Internal Medicine, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Istanbul University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Cytomegalovirus (CMV) and BK virus (BKV) are post-transplant opportunistic viral infections that affect patient and graft survival. This study was designed to evaluate the risk of BKV nephropathy and CMV disease in kidney transplant recipients who received induction therapy with ATG or basiliximab. MATERIAL AND METHODS We retrospectively analyzed information on 257 adult patients who underwent kidney transplantation between January 2007 and 2017. Patients were categorized into 3 groups according to the induction therapies. The primary endpoint was the onset of CMV disease or biopsy-confirmed BKV nephropathy. The secondary endpoints were biopsy-proven rejection episodes, graft loss, loss to follow-up, and death. RESULTS We followed 257 patients for a median of 55.5 months. The incidence of CMV disease was significantly higher in the only ATG group compared to the group without induction treatment (p<0.001). There was no significant difference in the incidence of BKV nephropathy among groups (p>0.05). The dosage of ATG (OR, 10.685; 95% CI, 1.343 5 to 85.009; P=0.025) was independent risk factor for death. CONCLUSIONS This study demonstrated that a higher dosage of ATG in high-risk patients is associated with an increased risk of CMV disease and patient death, also, reducing the dosage may be a rational strategy for increasing graft and patient's survival.

Indexed as

AdultBK VirusCytomegalovirusCytomegalovirus InfectionsFemaleHumansImmunosuppressive AgentsInduction ChemotherapyKidney TransplantationMaleMiddle AgedPolyomavirus InfectionsRetrospective StudiesRisk FactorsTumor Virus InfectionsYoung AdultImmunosuppressive Agents

Identifiers

PMID31296835
PMCPMC6652377
OpenAlexW2962192076

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.