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Case Report | Open Access2022|Volume 2|Issue 1| https://doi.org/10.37191/Mapsci-JASR-2(1)-015

Early Invasive Ventilation and Early Extubation to NIV– the Management of Covid-19 Patient with Severe Acute Respiratory Failure

ReceivedNov 8, 2021RevisedJan 7, 2022AcceptedDec 8, 2021PublishedJan 8, 2022

Salman Yahya1*, Rabia Azam1, Iftikhar Ahmed1 and Saqib Saleem1

1Department of Anaesthesia and Critical Care Bahria International Hospital, Bahria Orchard, Lahore, Pakistan 

*Corresponding Author: Salman Yahya, Department of Anaesthesia and Critical Care Bahria International Hospital, Bahria Orchard, Lahore, Pakistan.

Accepted Date: 12-08-2021; Published Date: 01-08-2022

Copyright© 2021 by Yahya S, et al. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

The covid-19 pandemic since its inception has reshaped many healthcare practices. One of the most severely affected specialty is intensive care and multiple strategies have been applied to deal with the severe covid-19 related pneumonia. This case report focuses on early invasive ventilation strategy versus delayed invasive ventilation strategies and early extubation and subsequent post-extubation support with Non-invasive ventilation strategies.

Keywords

COVID-19; Respiratory failure; ARDS; SARS-COV2. 

Introduction

The world is facing the novel Corona Virus-related COVID-19 disease since December 2019. It has been declared a global pandemic since March 11, 2020 [1]. The Corona Virus is a single-stranded RNA virus named SARS-CoV 2.

As of December 11, 2020, almost one year since the first case was reported in Wuhan China, the world has seen more than 68 million confirmed cases and more than 1.5 million deaths reported to World Health Organization (WHO). Most of the people (approximately 80%) infected with COVID-19 require no special treatment or hospitalization but some may develop serious illness [2]. Around 1 in 5 people infected with the virus acquire serious illness and develop respiratory distress of variable intensity requiring hospitalization. 

Among those admitted to the hospital 20-40% require critical care and deaths among those requiring critical care is around 40% globally.

Since the onset of the disease, the world has seen a huge number of studies, case reports, research, and data being published regarding the prevention, diagnosis, and management of the COVID-19 patient. In this case report, the key areas of management of a COVID-19 patient complicated by Acute Respiratory distress requiring invasive ventilation are outlined.

Background

Covid-19 symptoms usually start after 5 days of infection which includes fever, dry cough, body aches, and loss of taste and smell. After 12 days of infection, some people develop breathlessness and a more frequent cough. This is the stage where most people go to hospitals. It has been seen that people who are immunocompromised due to some chronic medical conditions have higher rates of medical admission with oxygen requirements than the healthy population. Researches and surveys all over the world have also reported higher ICU admissions and higher mortalities for these patients. 

Some patients do recover after Mechanical ventilation but develop long Covid-19 symptoms afterward. COV-SARS2 causes primarily a mix of respiratory, gastrointestinal, cardiovascular, and neurological, and thromboembolic disease with variable degrees of involvement of different organ systems. 

It was previously considered as mainly a respiratory system virus causing pneumonia of variable severity and acute respiratory distress syndrome [3]. It still mainly remains a respiratory system virus as bilateral pulmonary infiltrates with decreased levels of oxygenation in the blood are a frequent finding in most of the moderate to severe intensity cases. By the end of 2020, FDA approved many treatment strategies including monoclonal antibodies, steroids, and convalescent plasma for critical COV-SARS 2 patients. This case report includes a summary of patients who recovered without any plasma and tocilizumab administration just by following good intensive care pharmacological and mechanical strategies.

Case Report

A 39-year-old male was admitted with a history of fever for the last 10 days and shortness of breath for the last 2 days. The patient was previously not known to have any illness and was started on symptomatic treatment initially by a local general practitioner, but the condition did not improve. The patient was advised by GP to get SARS CoV-2 rPCR done and it came out to be positive on the 11th of May 2020. The patient got admitted on the 12th of May to the hospital and was maintaining saturation up to 93% on 5-6 liters of oxygen via facemask. 

On examination, the patient was found to be overweight having BMI of 29. The patient was a tachycardiac with a heart rate of 105/min, a temperature of 37.2 degrees Celsius, and a respiratory rate of 24/min while the rest of the examination was unremarkable. Patient inflammatory markers at admission were as follows: CRP-65, serum ferritin levels-61, and D-Dimer levels-190. The patient was started on methylprednisolone 40 mg twice daily (BiD) orally or via NGT, enoxaparin 80 mg BiD subcutaneously, and azithromycin 500 mg OD (as initial trials showed its immunomodulation role in mitigating excessive inflammation and benefit in tissue repair).

Orally along with symptomatic treatment for fever and cough. Chest X-ray at presentation showed bilateral patchy opacities and HRCT showed bilateral ground-glass haziness in lower and middle zones most dense posteriorly and slightly patchy anteriorly [3].

Three days after admission, the patient's respiratory compromise further worsened and the patient oxygen requirement increased drastically and was maintaining saturation only up to 86% at 15 L/min via a non-rebreather face mask. The patient was immediately shifted to ICU for further management. The patient eventually developed hypoxemic respiratory failure (type-1) which was confirmed on the arterial blood gas report. Patient Arterial blood gas showed PH of 7.3, PO2 of 6.5, and PCO2 of 5.5. The patient was initially started on CPAP but was unable to tolerate it for long and was desaturating to 82%. The patient was given CPAP trial for 6-8 hours.

Eventually, the patient was electively intubated and ventilated on pressure control mode with PEEP of 8 cm of H2O and pressure support of 20 cm of H2O with a respiratory rate of 15/min. The patient was kept sedated and paralyzed initially for the first 3 days. The patient remained hemodynamically stable till 3rd day of ICU admission. 

Ventilatory requirements, ECG, and CXR changes remain grossly unchanged in the initial 3 days. On day 4 of patient ICU admission, the patient developed sinus bradycardia and a sudden episode of desaturation which responded to maximum ventilatory support. 

Azithromycin was put on hold in response to bradycardia and borderline QT-interval [4]. The patient was continued on therapeutic thromboprophylaxis along with pneumatic compression devices.

PaO2:FiO2 showed mild ARDS with a value less than 300 mm of Hg [5]. The patient persistently started spiking fever from day 4 onwards of ventilation. Blood and sputum cultures were sent and the patient was started on Tanzocin 4.5g 6 Hourly as empirical therapy for VAP or septicemia [6]. The patient responded well to the change in treatment and fever also settled in the next 24 hours. From ventilatory day 6 onwards patient was regularly given sedation breaks and weaning trials.

FiO2 was gradually tapered down to 0.5 and PEEP to 5 cm of H2O. On day 7, the patient was given a spontaneous breathing trial with PS, which the patient tolerated quite well. The patient developed no fever in the last 24-48 hours and the patient inflammatory markers showed improvement. On the basis of clinical and laboratory numbers, the patient was eventually extubated on day 8 of IPPV. Patient Pre-Extubation ABGs showed PH of 7.42, PO2 of 8.5, and PCO2 of 4.5 After extubation. 

The patient remained on intermittent CPAP especially in the night times with high flow oxygen with FiO2 of 60% for the initial few days post-extubation. The patient also developed ICU delirium during the patient stay in the ICU which was treated with psychotherapy and anxiolytics. 

Oxygen requirement kept on decreasing as the patient was gradually mobilized out of bed. Chest physiotherapy and incentive spirometry was continued every 2 hours [7].

The patient also required extended physiotherapy to regain muscle strength [8]. The patient was eventually discharged from the hospital on the 17th day of patient admission. The patient remained on follow-up with Internal Medicine and Pulmonology for the initial 3 months and continued outpatient chest and limbs physiotherapy.

  

Figure 1: Post-intubation day 1 CXR.

 

Figure 2: Post-extubation day 2 CXR.

Summary of the Laboratory Values

LABS

Pre-Vent

Vent day 1

Vent day 2

Vent Day 5

Vent Day 6

Pre-Extubation

Post-Extubation Day 1

Pre- Discharge

PO2

63

95

89

93

-

95 (on 60% FiO2, PEEP of 8)

85

89 mmHg

LAC

-

2.7

1.7

-

1.5

-

-

-

Cr

0.7

0.9

0.9

-

-

-

0.8

0.6 mg/dL

Na

-

141

142

-

-

-

143

135 mEq/L

K

-

3.4

3.8

-

-

-

4

4.9 mmol/L

ALB

-

2.6

-

-

-

-

-

-

ALT

-

31

-

-

-

-

-

-

AST

-

20

-

-

-

-

-

-

Ferritin

61

-

80

300

-

-

-

-

PO2/FIO2

170

210

350

250

260

-

-

-

PCT (ng/ml)

0.08

1.5

-

0.05

-

CRP

38

170

53.8

30

20

-

10

6.7

D-DIMER (ng/)

190

-

-

600

-

-

200

-

WBC

-

11.3

10.4

15

13

-

12

10

Table 1: Summary of the laboratory values. 

Discussion

It causes primarily a mix of respiratory, gastrointestinal, cardiovascular, and neurological, and thromboembolic disease with variable degrees of involvement of different organ systems. It was previously considered as mainly a respiratory system virus causing pneumonia of variable severity and acute respiratory distress syndrome [9]. It still mainly remains a respiratory system virus as bilateral pulmonary infiltrates with decreased levels of oxygenation in the blood are a frequent finding in most of the moderate to severe intensity cases. Wearing masks, the practice of social distancing, and vaccination has significantly reduced the infection rate and its severity. Most of the world now is entering its 3rd or 4th wave with different variants. Dealing with the severe respiratory disease still largely remains a challenge for most intensive care units.

In this case report, early invasive ventilation strategy is emphasized in comparison to the NIV strategies in select young individuals who may benefit from this therapy along with steroids and other ICU supportive therapy. Also, early extubation to NIV despite the high FiO2 requirements and relatively higher PEEP values might be acceptable to avoid prolonged invasive ventilation and its complication. This strategy though might not be suitable for all kinds of patients, but it can be a useful strategy in select patients to avoid the initial harmful effects of prolonged NIV like pneumothorax and pneumo-mediastinum which can also make invasive ventilation even more challenging in already difficult patients.

Conclusion

1. Patients who have acute respiratory insult secondary to COV-SARS-2 in hospitals might benefit from early intubation and subsequent early extubation trial [10].

2. Early intubation may prevent lung injury in patients who breathe spontaneously and have high respiratory drive. Early invasive mechanical ventilation also acts as means to reduce aerosolization of virus in Covid-19 patients, as would happen alternately by high flow oxygenation or CPAP allowing air leaks. Contrary to some studies and clinical data suggest that ventilation in Covid-19 patients also put them at the risk of ventilator-associated pneumonia, lung injury, complications linked to sedatives and paralytics, and barotrauma.

3. Good sedation and ventilation in the initial few days can achieve good Ventilation/Perfusion ratios and thereby prevent/improve early ARDS [11].

4. Chest Physiotherapy, Posture Changing, and suctioning aids in alveolar recruitment along with preventing mucous plugging, and these strategies altogether enhance early weaning success. 

References

1. Prevention. Centre for Disease Control and. Global Covid 19. 2021.

2. Al-Aly Z, Xie Y, Bowe B. High-dimensional characterization of post-acute sequelae of COVID-19. Nature. 202;594(7862):259-64. PubMed | CrossRef

3. Cleverley J, Piper J, Jones MM. The role of chest radiography in confirming covid-19 pneumonia. BMJ. 2020;370. PubMed | CrossRef

4. Benn K, Salman S, Page-Sharp M, Davis TM, Buttery JP. Bradycardia and hypothermia complicating azithromycin treatment. Am J Case Rep. 2017;18:883. PubMed | CrossRef

5. Tan AE, Beither JR, Brochard L, Calfee C, Slutsky AS. COVID-19 Associated ARDS. Lancet Respir Med. 2020;8. PubMed | CrossRef

6. Maes M, Higginson E, Pereira-Dias J, Curran MD, Parmar S, Khokhar F, et al. Ventilator-associated pneumonia in critically ill patients with COVID-19. Crit Care. 2021;25(1):1-1. 

7. Jones AY. Intensive care physiotherapy-Medical staff perceptions. Hong Kong Physiother J. 2001;19(1):9-16. 

8. Behbehani NA, Al-Mane F, D’yachkova Y, Paré P, Gerald JM. Myopathy following mechanical ventilation for acute severe asthma: the role of muscle relaxants and corticosteroids. Chest. 1999;115(6):1627-31. PubMed | CrossRef

9. Zaim S, Chong JH, Sankaranarayanan V, Harky A. COVID-19 and multiorgan response. Curr Probl Cardiol. 2020;45(8):100618. PubMed | CrossRef

10. Hyman JB, Leibner ES, Tandon P, Egorova NN, Bassily-Marcus A, Kohli-Seth R, et al. Timing of intubation and in-hospital mortality in patients with coronavirus disease 2019. Crit Care Explor. 2020;2(10). PubMed | CrossRef

11. Chanques G, Constantin JM, Devlin JW, Ely EW, Fraser GL, Gélinas C, et al. Analgesia and sedation in patients with ARDS. Intensive Care Med. 2020:1-5. PubMed | CrossRef


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