Evidence map›Paper›PMID 35748549›Full record

ReviewCurrent drug targets2022

Therapeutic Approaches for Combating

Aruna Punia, Pooja Choudhary, Namita Sharma, Sweety Dahiya, Prity Gulia, Anil K Chhillar

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current drug targets, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Frontiers in microbiology · 2023
    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

6 authors.

Aruna PuniaDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.
Pooja ChoudharyDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.
Namita SharmaDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.
Sweety DahiyaDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.
Prity GuliaDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.
Anil K ChhillarDepartment of Biotechnology, Maharishi Dayanand University, Rohtak, Haryana 124001, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Now-a-days fungal infection emerges as a significant problem to healthcare management systems due to high frequency of associated morbidity, mortality toxicity, drug-drug interactions, and resistance of the antifungal agents. Aspergillus is the most common mold that cause infection in immunocompromised hosts. It's a hyaline mold that is cosmopolitan and ubiquitous in nature. Aspergillus infects around 10 million population each year with a mortality rate of 30-90%. Clinically available antifungal formulations are restricted to four classes (i.e., polyene, triazole, echinocandin, and allylamine), and each of them have their own limitations associated with the activity spectrum, the emergence of resistance, and toxicity. Consequently, novel antifungal agents with modified and altered chemical structures are required to combat these invasive fungal infections. To overcome these limitations, there is an urgent need for new antifungal agents that can act as potent drugs in near future. Currently, some compounds have shown effective antifungal activity. In this review article, we have discussed all potential antifungal therapies that contain old antifungal drugs, combination therapies, and recent novel antifungal formulations, with a focus on the Aspergillus associated infections.

Indexed as

Antifungal AgentsAspergillosisMycosesAspergillusDrug Resistance, FungalEchinocandinsHumansAntifungal AgentsEchinocandinsAspergillusazolesechinocandinsinvasive aspergillosisnovel drugspolyenes

Identifiers

PMID35748549

What Socratic holds

Textmetadata
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 Socratic graph.