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. 2020 Sep 7;67:110037. doi: 10.1016/j.jclinane.2020.110037

Perioperative management of COVID 19 patients undergoing coronary artery bypass surgery

Bassam Shoman 1, Amr Salah Omar 1,, Abdulaziz Alkhulaifi 1, Cornelia Carr 1, Suraj Sudarsanan 1, Sameh Abouelnaga 1, Hesham Ewila 1
PMCID: PMC7476605  PMID: 32920345

Highlights

  • COVID-19 represents a major challenge for healthcare systems globally and regionally.

  • The complexity of the disease requires special considerations when cardiac surgery is imminent.

  • Worsening of the patients’ clinical condition because of COVID-19 association was not encountered in our series.

  • Healthcare providers might not endure cross-infection if strict protocol is followed.


Dear Editor:

The pandemic caused by the coronavirus disease 2019 (COVID-19) placed the health care system worldwide under great pressure. Certain facilities were forced to postpone elective surgical procedures when the severity of the pandemic increased [1]. The high contiguity of COVID-19 placed the cardiac surgery societies in a position to release guiding documents aiming at practitioner's exposure risk reduction and adequate resources allocation.

We are reporting three COVID-19 positive cases, without respiratory symptoms, that were diagnosed to have critical coronary artery disease underwent urgent coronary surgery to highlight the key points in their perioperative management. The project was by the Hamad medical corporation center, (IRB MRC 04-20-586).

The complexity in the decision to operate on urgent basis on patient with a recent diagnosis of COVID-19 came from the novelty of the disease and limited abilities to define its impact on cardiothoracic surgical outcome. Our experience with three such patients represents pragmatic decision to operate. The apparent respiratory system stability of these patients encouraged our team to give priority to manage their acute coronary syndrome (ACS) to limit the possible mortality and morbidity.

Our institute elected to do reverse transcription polymerase chain reaction (RT-PCR) from nasopharyngeal swab test for all patients presenting with ACS. Patients were considered to be COVID positive (unless proved otherwise by testing) and practitioners coming in contact with such patients used personal protective equipment (PPE). It is imperative that ACS should be managed without waiting for COVID-19 test results [2].

In our center we sat a multidisciplinary meeting before deciding to operate on COVID-19 positive patients. The contagious time for COVID-19 patients, who are asymptomatic and remain positive, plus the possible effects of cardiopulmonary bypass on patients who are supposedly active are currently unknown; therefore, they undergo management as infectious and active and it was settled to operate on and to care for these patients in full PPE [3]. The anatomical complexity of the coronary lesions in our three patients made surgery the only hopeful solution.

We designated one operating room in our facility to receive COVID-19 positive. We prepared a flow chart for team guidance (Fig. 1 ). In our three patients, anesthesia induction was carried out after 5 min facemask pre‑oxygenation, by rapid sequence intubation (RSI) technique. Endotracheal intubation was done by video-laryngoscopy utilizing apneic technique without manual ventilation. Peng and Hota suggested that apneic intubation technique confers highest success probability for COVID-19 patients [4].

Fig. 1.

Fig. 1

Periopaertaive follow chart for patient with COVID-19.

We asked the ICU team to receive the patient form the theatre door to minimize PPE exhaustion and to limit staff mobility in contaminated PPE. Transport was carried out with a transport ventilator and minimum team. Patel and colleagues raised the importance of minimizing ventilator circuit disconnection, reducing staff attendance and ventilator transport [5].

Safety of COVID-19 patients transport needs to be customized in each institute. We transfer positive cases to a specific unit, which has negative-pressure rooms with additional HEPA filters. Lung protective strategy, early thromboembolic prophylaxis and extubation in a protected atmosphere were followed. None of our patients exhibited early complications and were discharged from the ICU after an average of 24 h after surgery.

We followed up our patients routinely, like all other post-cardiac surgical patients, with special attention to the early complications we already highlighted. We screened our exposed practitioners routinely after 3 days by COVID-19 IgM-IgG Rapid Test “BioMedomics, USA” or if they experience symptoms related to COVID-19 infection by RT-PCR.

1. Conclusion

In our case series we did not experience worsening of the patients' clinical condition due to COVID-19 association. None of the health care providers attending to the patients endured cross infection. These results need to be confirmed in further trials.

Abbreviations

CAD

coronary artery disease

CABG

coronary artery bypass graft

COVID-19

coronavirus disease 2019

CTICU

cardiothoracic intensive care unit

PPE

personal protective equipment

SARS-CoV-2

acute respiratory syndrome coronavirus-2

NSTEMI

Non-ST segment elevation myocardial infarction

CRediT authorship contribution statement

BS: study design, contribution to the concepts, writing the manuscript and revising the final form. AK: critical revision, CC: patients' s enrollment; ASO: writing and manuscript revision; SS: data management and manuscript revision, HE data collection, SE data management, cases review. All authors read and approved the final manuscript.

Declaration of competing interest

The authors declare that they have no competing interests.

Acknowledgments

Acknowledgment

This work would not have been possible without the kind support and help of many individuals and our organization. The authors thank all members of the Cardiothoracic surgery department, Heart Hospital, of Hamad Medical Corporation, Qatar, for extensive work during this hard time and for providing the required data. The authors also thank the members of the medical research department of Hamad Medical Corporation for their support throughout this project.

Funding

The study was funded by Hamad medical corporation, medical research center, Doha, Qatar (reference number MRC 04-20-586). The medical research center in Hamad Medical Corporation take the account in the publication of this manuscript.

Availability of data and materials

The data related to this manuscript and to its conclusions are available in the Hamad medical corporation medical research center. The data is available on request to the corresponding author Dr. Amr Salah Omar by e-mail: a_s_omar@yahoo.com, after approval from the medical research center.

Consent for publication

Not applicable.

Ethics approval and consent to participate

This study was approved by medical research center in Hamad Medical Corporation. The ethical committee in Hamad medical corporation approved the study (reference number MRC 04-20-586), informed consent was waived by the ethical review panel for all patients enrolled in the study. However, all study data were maintained anonymously.

References

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data related to this manuscript and to its conclusions are available in the Hamad medical corporation medical research center. The data is available on request to the corresponding author Dr. Amr Salah Omar by e-mail: a_s_omar@yahoo.com, after approval from the medical research center.


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