Literature DB >> 35662783

Venlafaxine-induced interstitial lung disease with COVID-19 pandemic-related depression.

Akihito Okazaki1, Katsunao Kita2.   

Abstract

Venlafaxine-associated pulmonary toxicity is rare, with only a few reports of pneumonitis, eosinophilic pneumonia, and asthma. We report a case of venlafaxine-induced interstitial lung disease in a patient with coronavirus disease 2019 pandemic-related depression. Chest imaging findings improved after discontinuation of venlafaxine and treatment with corticosteroids.
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Entities:  

Keywords:  drug‐induced pneumonitis; venlafaxine

Year:  2022        PMID: 35662783      PMCID: PMC9163472          DOI: 10.1002/ccr3.5941

Source DB:  PubMed          Journal:  Clin Case Rep        ISSN: 2050-0904


CASE PRESENTATION

A 73‐year‐old woman with treatment‐free Sjogren's syndrome was hospitalized for depression related to the coronavirus disease 2019 (COVID‐19) pandemic, and venlafaxine was initiated. There were no pulmonary lesions on admission (Figure 1, 2). Two months after starting treatment, the patient complained of dry cough, and chest imaging revealed bilateral multiple ground‐glass opacities, consolidation, and small bilateral pleural effusions (Figure 1, 2). Polymerase chain reaction assay for COVID‐19 was negative. Laboratory findings revealed elevated surfactant protein‐D (187 ng/ml) and C‐reactive protein (15.7 mg/dl), normal Krebs von den Lungen‐6 (306 U/ml), and no novel autoantibodies compared with baseline. Bronchoalveolar lavage fluid was predominantly lymphocytic (82%). Venlafaxine discontinuation and treatment with corticosteroids improved imaging findings (Figure 1C).
FIGURE 1

(A) Chest radiograph showing no pulmonary lesions on admission. (B) Chest radiograph 2 months after venlafaxine treatment showing bilateral multiple opacities

FIGURE 2

(A) Chest CT with no pulmonary lesions on admission. (B) Chest CT showing bilateral multiple ground‐glass opacities, consolidation, and small bilateral pleural effusions 2 months after venlafaxine treatment. (C) Chest CT revealing remarkable improvement 3 months after discontinuation of venlafaxine and corticosteroid treatment. Regarding corticosteroid administration, 500 mg methylprednisolone was first administered for 3 days, then tapered to 40 mg/day prednisolone and then discontinued over 3 months. A probable relationship between venlafaxine and interstitial lung disease was obtained with an Adverse Drug Reaction Probability Score (Naranjo nomogram) of 7. Abbreviation: CT, computed tomography

(A) Chest radiograph showing no pulmonary lesions on admission. (B) Chest radiograph 2 months after venlafaxine treatment showing bilateral multiple opacities (A) Chest CT with no pulmonary lesions on admission. (B) Chest CT showing bilateral multiple ground‐glass opacities, consolidation, and small bilateral pleural effusions 2 months after venlafaxine treatment. (C) Chest CT revealing remarkable improvement 3 months after discontinuation of venlafaxine and corticosteroid treatment. Regarding corticosteroid administration, 500 mg methylprednisolone was first administered for 3 days, then tapered to 40 mg/day prednisolone and then discontinued over 3 months. A probable relationship between venlafaxine and interstitial lung disease was obtained with an Adverse Drug Reaction Probability Score (Naranjo nomogram) of 7. Abbreviation: CT, computed tomography

DISCUSSION AND CONCLUSION

The COVID‐19 pandemic shows no sign of abating, and its negative impact on mental health is a major social problem worldwide. The prevalence of pandemic‐related depression in the general population is estimated at 14.3%–24.3%. Venlafaxine, a serotonin‐noradrenaline reuptake inhibitor, is used to treat depression worldwide. Venlafaxine‐associated pulmonary toxicity is rare, with only a few reports of pneumonitis, eosinophilic pneumonia, and asthma. This rare pulmonary side effect of venlafaxine should be promptly diagnosed and treated to improve patient outcomes.

AUTHOR CONTRIBUTIONS

AO was responsible for manuscript drafting and image modification. KK was responsible for psychiatric diagnosis. Both authors were directly involved in the treatment of the patient, critically revised the manuscript, and approved the final version.

CONFLICT OF INTEREST

None.

CONSENT

Written informed consent to publish this report was obtained from the patient before the submission process.
  3 in total

1.  Venlafaxine-induced interstitial lung disease with COVID-19 pandemic-related depression.

Authors:  Akihito Okazaki; Katsunao Kita
Journal:  Clin Case Rep       Date:  2022-06-02

2.  Desvenlafaxine-Induced Interstitial Pneumonitis: A Case Report.

Authors:  Arjan Flora; Daniel Pipoly
Journal:  Drug Saf Case Rep       Date:  2018-01-17
  3 in total
  1 in total

1.  Venlafaxine-induced interstitial lung disease with COVID-19 pandemic-related depression.

Authors:  Akihito Okazaki; Katsunao Kita
Journal:  Clin Case Rep       Date:  2022-06-02
  1 in total

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