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. 2021 Feb 10;24(2):143–145. doi: 10.1007/s11102-021-01130-x

Glucocorticoid use in patients with adrenal insufficiency following administration of the COVID-19 vaccine: a pituitary society statement

Laurence Katznelson 1,, Mônica Gadelha 2
PMCID: PMC7872824  PMID: 33564969

Abstract

Purpose

Side effects of the coronavirus disease 2019 (COVID-19) vaccines include pain at the injection site, fatigue, headache, myalgias, arthralgias, chills, and fever, all of which can be early indicators of an increased need for glucocorticoid replacement in patients with adrenal insufficiency. The Pituitary Society surveyed its membership to understand planned approaches to glucocorticoid management in patients with adrenal insufficiency who will receive a COVID-19 vaccine.

Methods

Members were asked to complete up to 3 questions regarding their planned approach for use of glucocorticoid replacement in patients with proven adrenal insufficiency.

Results

Surveys were sent to 273 members and 103 responded. Thirty-six percent plan to recommend that patients automatically increase glucocorticoid dosage with administration of the first vaccine injection. Of these, 84% plan to increase glucocorticoid dose on the day of vaccination, and 49% plan to increase glucocorticoid dose prior to vaccination. Of the 64% who do not plan to recommend automatic glucocorticoid dose increase with vaccine administration, 88% plan to increase the dose if the patient develops a fever, and 47% plan to increase the dose if myalgias and arthralgias occur.

Conclusions

Most clinicians plan to maintain the current glucocorticoid dose with vaccine administration. The vast majority plan and to increase glucocorticoid dose in case of fever, and just under half in case of arthralgias and myalgias. These survey results offer suggested management guidance for glucocorticoid management in patients with adrenal insufficiency.

Keywords: Adrenal insufficiency, COVID-19, Vaccines, Glucocorticoid replacement


Availability of vaccines is a giant step in combating the coronavirus disease 2019 (COVID-19) pandemic. Side effects of the Pfizer-BioNTech and Moderna vaccines include up to several days of pain at the injection site, fatigue, headache, myalgias, arthralgias, chills, and fever [1, 2]. These signs and symptoms can be early indicators of an increased need for glucocorticoid replacement in patients with adrenal insufficiency [3, 4]. Other than a case report of adrenal crisis in a patient with Addison’s disease following routine administration of influenza, Tdap, and pneumococcal vaccines [5], there is no information on routine management of primary or secondary adrenal insufficiency following administration of these vaccines, and we do not yet know the potential impact of glucocorticoids on immune response to the vaccine.

The Pituitary Society surveyed its membership to understand planned approaches to glucocorticoid management in patients with adrenal insufficiency who will receive a COVID-19 vaccine with a goal of using survey results to inform the larger community of suggested best practices.

Surveys were developed using SurveyMonkey (San Mateo, CA) with branch logic. Members were asked to complete up to 3 questions regarding their planned approach for use of glucocorticoid replacement in patients with proven adrenal insufficiency (Table 1). The survey was closed after 3 days and results were collected and analyzed.

Table 1.

Survey questions

Question 1

Following administration of the COVID-19 vaccine in a patient with proven adrenal insufficiency, do you plan to recommend that your patient automatically increase the glucocorticoid dosage?

 If yes, answer questions 2 & 3

 If no, answer questions 4 & 5

Question 2

If the answer to question 1 was YES, will you recommend raising the glucocorticoid dose prior to the vaccination?

 If yes, go to question 3

 If no, go to question 3

Question 3

If the answer to question 1 was YES, will you recommend raising the dose on the day of the vaccination?

 If yes, end questionnaire

 If no, end questionnaire

Question 4

If the answer to question 1 was NO, will you recommend that the patient increase the glucocorticoid dose for fever?

 If yes, go to question 5

 If no, go to question 5

Question 5

If the answer to question 1 was NO, will you recommend that the patient increase the glucocorticoid dose for muscle and joint pains?

 If yes, end questionnaire

 If no, end questionnaire

Surveys were sent to 273 members and 103 responded (38% response rate). As shown in Fig. 1, 36% (37/103) plan to recommend that patients automatically increase their glucocorticoid dosage with administration of the first vaccine injection. Of these, 84% (31/37) plan to increase glucocorticoid dose on the day of vaccination, and 49% (18/37) plan to increase glucocorticoid dose prior to vaccination.

Fig. 1.

Fig. 1

Survey responses

By contrast, 64% (66/103) do not plan to recommend an automatic glucocorticoid dose increase with vaccine administration. Of these, 88% (58/66) plan to increase the dose if the patient develops a fever following administration, and 47% (31/66) plan to increase the dose if myalgias and arthralgias occur.

Thus, most clinicians plan to maintain the current glucocorticoid dose with vaccine administration. The vast majority of these clinicians plan to increase glucocorticoid dose with fever, and just under half plan to increase the dose with associated arthralgias and myalgias, known vaccine side effects.

These survey results offer a glimpse into the planned approach of our members for glucocorticoid management in patients with adrenal insufficiency. This survey does not reflect results of a trial on efficacy of glucocorticoid management in patients receiving the vaccine nor the impact of a particular glucocorticoid dose on the vaccine immune response. Importantly, these results do offer suggested management guidance based on responses from experienced clinicians treating pituitary diseases.

Acknowledgements

The authors thank Dr. A.J. van der Lely, President, and Bari Laner, Director, of the Pituitary Society for assistance with this project.

Funding

Development of this manuscript was supported by the Pituitary Society, for which Dr. Gadelha is President-Elect. The authors did not receive support from any organization for the submitted work.

Compliance with ethical standards

Conflict of interest

The authors have no relevant financial or non-financial interests to disclose.

Footnotes

Publisher's Note

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References


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