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1.
Clin Case Rep ; 11(6): e7455, 2023 Jun.
Article in English | MEDLINE | ID: covidwho-20242265

ABSTRACT

Although immunodeficient patients are less prone to develop Coronavirus disease 2019 (COVID-19)-mediated cytokine storm, secondary infections can cause serious complications in this vulnerable population. They are more likely to develop opportunistic infections that can mimic the symptoms of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Herein, we presented a 27-year-old male patient of SARS-CoV-2 infection, who was complicated with Pneumocystis jirovecii pneumonia (PJP), following treatment with rituximab. First, he was hospitalized for 5 days with fever, cough, and dyspnea due to COVID-19 infection, and treated with remdesivir and glucocorticoid. Then, he has been referred to our center with cough, dyspnea, body pain, and fever. Due to persistent fever, the progression of pulmonary lesions, and reduced oxygen saturation, we began treatment with piperacillin + tazobactam, vancomycin, and levofloxacin. Nevertheless, the patient's fever did not stop after the aforementioned empiric treatment and his condition got worse and he was admitted to the intensive care unit. The result of BAL fluid, tested for P. jirovecii by RT-PCR, turned out to be positive. Therefore, we started trimethoprim-sulfamethoxazole and dexamethasone, which improved his condition. We hope this article helps clinicians consider causes other than COVID-19, especially opportunistic infections such as PJP, in patients with respiratory symptoms and fever.

3.
Journal of Modern Medicine & Health ; 38(24):4195-4200, 2022.
Article in Chinese | Academic Search Complete | ID: covidwho-2201252

ABSTRACT

Objective To compare the computed tomography (CT) signs of Corona Virus Disease 2019 (COVID-19) and pneumocystis jirovecii pneumonia (PJP),and improve the level of differential diagnosis.Methods The first CT data of 32 COVID-19 patients admitted to Bao Ding No.1 Central Hospital and Bao Ding infectious Diseases Hospital of Hebei Province and 10 PJP patients admitted to Bao Ding No.1 Central Hospital of Hebei Province from December 2019 to March 2020 were collected, and their CT signs were compared.Results The COVID-19 patients were mainly characterized by multiple lung lesions in subpleural area, and their probability of pleural parallel sign and vascular thickening sign were significantly higher than those of the PJP patients, while the probability of pulmonary balloon sign, lunar arch sign and map sign were significantly lower than those of the PJP patients, with statistical significance (P<0.05) .Conclusion COVID-19 and PJP not only share common CT features but also have typical imaging features and chest CT plays an important role in the differential diagnosis of COVID-19 and PJP. (English) [ FROM AUTHOR]

4.
Medicina (Kaunas) ; 58(9)2022 Aug 24.
Article in English | MEDLINE | ID: covidwho-1997708

ABSTRACT

Here, we report two cases of patients with interstitial pneumonia (IP) on steroids who developed Pneumocystis jirovecii pneumonia (PJP) following coronavirus disease 2019 (COVID-19) infection. Case 1: A 69-year-old man on 10 mg of prednisolone (PSL) daily for IP developed new pneumonia shortly after his COVID-19 infection improved and was diagnosed with PJP based on chest computed tomography (CT) findings and elevated serum ß-D-glucan levels. Trimethoprim-sulfamethoxazole (TMP-SMZ) was administered, and the pneumonia resolved. Case 2: A 70-year-old woman taking 4 mg/day of PSL for IP and rheumatoid arthritis developed COVID-19 pneumonia, which resolved mildly, but her pneumonia flared up and was diagnosed as PJP based on CT findings, elevated ß-D-glucan levels, and positive polymerase chain reaction for P. jirovecii DNA in the sputum. The autopsy revealed diffuse alveolar damage, increased collagen fiver and fibrotic foci, mucinous component accumulation, and the presence of a P. jirovecii cyst. In conclusion, steroids and immunosuppressive medications are well-known risk factors for PJP. Patients with IP who have been taking these drugs for a long time are frequently treated with additional steroids for COVID-19; thus, PJP complications should be avoided in such cases.


Subject(s)
COVID-19 , Lung Diseases, Interstitial , Pneumocystis carinii , Pneumonia, Pneumocystis , Aged , COVID-19/complications , Female , Glucans/therapeutic use , Humans , Lung Diseases, Interstitial/complications , Lung Diseases, Interstitial/drug therapy , Male , Pneumocystis carinii/genetics , Pneumonia, Pneumocystis/complications , Pneumonia, Pneumocystis/drug therapy , Prednisolone/therapeutic use , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
5.
Open Forum Infect Dis ; 9(6): ofac076, 2022 Jun.
Article in English | MEDLINE | ID: covidwho-1908872

ABSTRACT

This study aimed to investigate the impact of nationwide nonpharmaceutical interventions against coronavirus disease 2019 (COVID-19) on the incidence of Pneumocystis jirovecii pneumonia (PCP) in kidney transplant recipients. The monthly incidence of PCP during the COVID-19 period decreased significantly compared to that of the pre-COVID-19 period in kidney transplant recipients.

6.
J Fungi (Basel) ; 8(6)2022 May 30.
Article in English | MEDLINE | ID: covidwho-1869675

ABSTRACT

Coronavirus disease 2019 (COVID-19) may occur with concurrent infections caused by bacterial and fungal microorganisms. This systematic review evaluated studies reporting concomitant COVID-19 and Pneumocystis jirovecii pneumonia (PJP). We found 39 patients (74% male, median age: 56.8 (range: 11-83) years), including 66% immunosuppressed individuals (23% HIV-infected and 41% on long-term corticosteroid therapy). Patients were characteristically severely ill (mechanical ventilation: 70%), associated with 41% mortality. The median lymphocyte count was 527 cells/mm3 (range: 110-2200), and the median CD4+ T cell count was 206 cells/mm3 (range: 8-1021). We identified three patterns of concurrent COVID-19 and P. jirovecii infection. The first pattern (airway colonization with a low burden of P. jirovecii) does not seem to modify the COVID-19 course of illness. However, P. jirovecii superinfection, typically occurring weeks after COVID-19 diagnosis as a biphasic illness, and P. jirovecii coinfection characteristically results in progressive multilobar pneumonia, which is associated with poor outcomes. To support this categorization, we reported three patients with concurrent PJP and COVID-19 identified in our institution, presenting these clinical scenarios. The diagnosis of PJP requires a high index of suspicion, since clinical and radiological characteristics overlap with COVID-19. Observational studies are necessary to determine the PJP burden in patients with COVID-19 requiring hospitalization.

7.
Int J STD AIDS ; 33(2): 209-211, 2022 02.
Article in English | MEDLINE | ID: covidwho-1542033

ABSTRACT

We describe the case of a 30-year-old care home employee diagnosed with COVID-19 and acute untreated HIV-1. He was unable to return to work for 119 days due to concerns over transmission risk as his SARS-CoV-2 PCR remained detectable. This highlights the uncertainty in interpreting SARS-CoV-2 PCR results post-infection in acute untreated HIV.


Subject(s)
COVID-19 , HIV Infections , HIV-1 , Adult , HIV Infections/complications , HIV Infections/drug therapy , Humans , Male , Return to Work , SARS-CoV-2
8.
Clin Exp Med ; 22(3): 327-346, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-1368499

ABSTRACT

Treatment of the novel Coronavirus Disease 2019 (COVID-19) remains a complicated challenge, especially among patients with severe disease. In recent studies, immunosuppressive therapy has shown promising results for control of the cytokine storm syndrome (CSS) in severe cases of COVID-19. However, it is well documented that immunosuppressive agents (e.g., corticosteroids and cytokine blockers) increase the risk of opportunistic infections. On the other hand, several opportunistic infections were reported in COVID-19 patients, including Aspergillus spp., Candida spp., Cryptococcus neoformans, Pneumocystis jiroveci (carinii), mucormycosis, Cytomegalovirus (CMV), Herpes simplex virus (HSV), Strongyloides stercoralis, Mycobacterium tuberculosis, and Toxoplasma gondii. This review is a snapshot about the main opportunistic infections that reported among COVID-19 patients. As such, we summarized information about the main immunosuppressive agents that were used in recent clinical trials for COVID-19 patients and the risk of opportunistic infections following these treatments. We also discussed about the main challenges regarding diagnosis and treatment of COVID-19-associated opportunistic infections (CAOIs).


Subject(s)
COVID-19 Drug Treatment , COVID-19 , Candidiasis , Cytomegalovirus Infections , Opportunistic Infections , Pneumonia, Pneumocystis , COVID-19/complications , Candidiasis/complications , Cytomegalovirus Infections/drug therapy , Humans , Immunosuppressive Agents/therapeutic use , Opportunistic Infections/complications , Opportunistic Infections/drug therapy , Opportunistic Infections/epidemiology , Pneumonia, Pneumocystis/etiology
9.
Infection ; 49(6): 1079-1090, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1248754

ABSTRACT

BACKGROUND: Pneumocystis jirovecii (P. jirovecii) is increasingly identified on lower respiratory tract specimens of COVID-19 patients. Our narrative review aims to determine whether the diagnosis of pneumocystis jirovecii pneumonia (PJP) in COVID-19 patients represents coinfection or colonization based on the evidence available in the literature. We also discuss the decision to treat COVID-19 patients with coinfection by PJP. METHODS: A literature search was performed through the Pubmed and Web of Science databases from inception to March 10, 2021. RESULTS: We identified 12 COVID-19 patients suspected to have PJP coinfection. All patients were critically ill and required mechanical ventilation. Many were immunosuppressed from HIV or long-term corticosteroids and other immunosuppressive agents. In both the HIV and non-HIV groups, severe lymphocytopenia was encountered with absolute lymphocyte and CD4+T cell count less than 900 and 200 cells/mm, respectively. The time to PJP diagnosis from the initial presentation was 7.8 (range 2-21) days. Serum lactate dehydrogenase and beta-D-glucan were elevated in those coinfected with PJP. All patients were treated with anti-PJP therapy, predominantly sulfamethoxazole-trimethoprim with corticosteroids. The overall mortality rate was 41.6%, and comparable for both HIV and non-HIV groups. CONCLUSION: As the current evidence is restricted to case reports, the true incidence, risk factors, and prognosis of COVID-19 patients with PJP coinfections cannot be accurately determined. Comorbidities of poorly controlled HIV with lymphocytopenia and multiple immunosuppressive therapies are likely predisposing factors for PJP coinfection.


Subject(s)
COVID-19 , Coinfection , Pneumocystis carinii , Pneumonia, Pneumocystis , Coinfection/epidemiology , Humans , Pneumonia, Pneumocystis/diagnosis , Pneumonia, Pneumocystis/drug therapy , Pneumonia, Pneumocystis/epidemiology , SARS-CoV-2
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