Evidence map›Paper›PMID 39988835›Full record

ArticleThe American journal of case reports2025

Severe COVID-19 Pneumonia, Opportunistic Candida krusei Infection, and Acute Respiratory Distress Syndrome with Pulmonary Arterial Hypertension Treated with Bosentan: A Case Report.

Killen H Briones-Claudett, Killen H Briones-Zamora, Jaime Galo Benites Solis, Doménica I Huilcapi Borja, Karelys Nicole Arteaga Ocaña, Maria Antonieta Touriz Bonifaz, Pedro Barberan-Torres, Michelle Grunauer

Abstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Killen H Briones-ClaudettFaculty of Medical, Health and Life Sciences, Universidad Internacional del Ecuador, UIDE, Quito, Ecuador.ORCID 0000-0002-7778-0362
Killen H Briones-ZamoraFaculty of Medical Sciences, Universidad Espíritu Santo, Samborondón, Ecuador.ORCID 0000-0003-2732-7022
Jaime Galo Benites SolisIntensive Care Unit, Omni Hospital, Guayaquil, Ecuador.ORCID 0009-0001-8718-3385
Doménica I Huilcapi BorjaDepartment of Pulmonary and Intensive Care, Briones PulmoCare, Guayaquil, Ecuador.ORCID 0009-0007-8859-7751
Karelys Nicole Arteaga OcañaDepartment of Pulmonary and Intensive Care, Briones PulmoCare, Guayaquil, Ecuador.ORCID 0009-0002-8308-1020
Maria Antonieta Touriz BonifazFaculty of Medical Sciences, Universidad de Guayaquil, Guayaquil, Ecuador.
Pedro Barberan-TorresFaculty of Medical, Health and Life Sciences, Universidad Internacional del Ecuador, UIDE, Quito, Ecuador.ORCID 0000-0002-9489-9859
Michelle GrunauerSchool of Medicine, College of Health Sciences, Universidad San Francisco de Quito (USFQ), Quito, Ecuador.ORCID 0000-0002-5821-7603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Despite global vaccination efforts, COVID-19 still necessitates effective treatments for severe cases that can quickly escalate to life-threatening complications, such as acute respiratory distress syndrome (ARDS) and secondary pulmonary arterial hypertension (PAH). Here, we present the clinical journey of a 73-year-old Ecuadorian man who developed severe COVID-19 pneumonia complicated by an opportunistic Candida krusei infection and ARDS, subsequently progressing to long-term PAH, managed with bosentan, an endothelin 1 (ET-1) antagonist. CASE REPORT The patient, vaccinated with 2 doses of CoronaVac, experienced severe COVID-19 complications, including ARDS and secondary PAH, further complicated by a C. krusei infection. Despite prompt mechanical ventilation and intensive care, his condition rapidly deteriorated. Clinical evaluation confirmed COVID-19-associated ARDS, secondary PAH, and C. krusei infection through bronchoalveolar lavage. The therapeutic approach combined bosentan (125 mg twice daily) with dual antifungal therapy, leading to significant stabilization and eventual discharge. Post-discharge assessments showed persistent cardiopulmonary dysfunction, consistent with post-COVID-19 syndrome. CONCLUSIONS This case highlights critical COVID-19 complications in a vaccinated patient. While vaccination may provide substantial protection, COVID-19 pneumonia treated with corticosteroids can increase the risk of opportunistic infections like C. krusei, and ARDS can lead to pulmonary fibrosis and PAH. This case underscores the need for research on therapeutic strategies for complex COVID-19 cases and emphasizes comprehensive, personalized care for managing COVID-19 complications and sequelae.

Indexed as

Antihypertensive AgentsBosentanCandidiasisOpportunistic InfectionsPulmonary Arterial HypertensionRespiratory Distress SyndromeAgedCOVID-19HumansMalePandemicsSARS-CoV-2Antihypertensive AgentsBosentan

Identifiers

PMID39988835
PMCPMC11868965

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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.