Skip to main content
BMC Anesthesiology logoLink to BMC Anesthesiology
. 2021 Jan 8;21:9. doi: 10.1186/s12871-020-01221-5

SARS-CoV-2 pneumonia succesfully treated with cpap and cycles of tripod position: a case report

Michela Rauseo 1, Lucia Mirabella 1, Rosa Roberta Caporusso 1, Leonarda Pia Cantatore 1, Marco Paolo Perrini 1, Paolo Vetuschi 1, Daniela La Bella 1, Livio Tullo 1, Gilda Cinnella 1,
PMCID: PMC7791159  PMID: 33419396

Abstract

Background

Pneumonia induced by 2019 Coronavirus (COVID-19) is characterized by hypoxemic respiratory failure that may present with a broad spectrum of clinical phenotypes. At the beginning, patients may have normal lung compliance and be responsive to noninvasive ventilatory support, such as CPAP. However, the transition to more severe respiratory failure - Severe Acute Respiratory Syndrome (SARS-CoV-2), necessitating invasive ventilation is often abrupt and characterized by a severe V/Q mismatch that require cycles of prone positioning. The aim of this case is to report the effect on gas exchange, respiratory mechanics and hemodynamics of tripod (or orthopneic sitting position) used as an alternative to prone position in a patient with mild SARS-CoV-2 pneumonia ventilated with helmet CPAP.

Case presentation

A 77-year-old awake and collaborating male patient with mild SARS-CoV-2 pneumonia and ventilated with Helmet CPAP, showed sudden worsening of gas exchange without dyspnea. After an unsuccessful attempt of prone positioning, we alternated three-hours cycles of semi-recumbent and tripod position, still keeping him in CPAP. Arterial blood gases (PaO2/FiO2, PaO2, SaO2, PaCO2 and A/a gradient), respiratory (VE, VT, RR) and hemodynamic parameters (HR, MAP) were collected in the supine and tripod position. Cycles of tripod position were continued for 3 days. The patient had a clinically important improvement in arterial blood gases and respiratory parameters, with stable hemodynamic and was successfully weaned and discharged to ward 10 days after pneumonia onset.

Conclusions

Tripod position during Helmet CPAP can be applied safely in patients with mild SARS-CoV-2 pneumonia, with improvement of oxygenation and V/Q matching, thus reducing the need for intubation.

Keywords: COVID-19, SARS-CoV-2 pneumonia, Helmet CPAP, Tripod position

Background

Hypoxemic respiratory failure is the characteristic aspect for presentation of pneumonia induced by 2019 Coronavirus (COVID-19). SARS-CoV-2 patients present with a wide spectrum of clinical severity, ranging from asymptomatic to pneumonia to ARDS-like phenotypes [1, 2]. In the making of more robust evidence, widely shared hypothesis suggests that together with viral load and patient’s physiological reserve, the activation’s amplitude of two biological cascades, the interleukin 6 (IL-6) cytokine storm [3] and the disseminated intravascular cascade (DIC) [4], are responsible for the inflammatory host response in the lungs.

At the beginning, patients may have normal lung compliance and be responsive to noninvasive ventilatory support, such as CPAP. However, the transition to more severe respiratory failure - Severe Acute Respiratory Syndrome (SARS-CoV-2), necessitating invasive ventilation is often abrupt and characterized by a severe V/Q mismatch that require cycles of prone positioning [2, 5].

We report on the clinical course of a patient suffering from refractory hypoxemia due to COVID-19 pneumonia treated with CPAP and helmet interface in the out of bed tripod position (Fig. 1). We choose this solution, since the patient was well adapted to CPAP, but did not tolerate other facial interfaces nor prone position. Repeated shifting from supine to tripod determined a stable improvement of ventilation to perfusion (V/Q) matching and PaO2/FiO2 ratio and prevented intubation and invasive mechanical ventilation.

Fig. 1.

Fig. 1

Patient in tripod position during Helmet CPAP

Case presentation

A 77-year-old man was admitted to the emergency department (ER), on March 6th. His symptoms commenced on the previous day, while at home, with sore throat, dry cough, mild dyspnea and subjective fevers. He had been in contact in earlier days with an individual positive for COVID-19 disease, and was otherwise healthy. Physical examination revealed a temperature of 37 °C, pulse rate of 80 beat/min, mean blood pressure (mBP) 80 mmHg, respiratory rate (RR) 18 breath/min and oxygen saturation 87% in room air. SARS-CoV-2 was detected in a nasopharyngeal swab specimen by real-time reverse-transcriptase PCR. After having unsuccessfully been treated for 24 h with Venturi Mask Oxygen in the Infectious Diseases department, the patient was referred to our ICU and CPAP with helmet immediately started.

At ICU admission he had no fever, WBC 4.35*103 mcL and CRP of 120 mg/L. Chest X ray showed interstitial lung infiltrates, no sign of fatigue nor tachypnea.

On admission CPAP was set at 10 cmH2O with a FiO2 of 50%, in order to reach a VT of 6–7 ml/Kg PBW. Under such setting, the highest PaO2/FiO2 was 172, PaCO2 34 mmHg, pH 7.34, RR 20. On march 8th, PaO2/FiO2 decreased to 136 and CPAP was increased to 12 cmH2O, with FiO2 55%. PaO2/FiO2 further decreased and helmet was then temporarily substituted with a full face mask in order to position him prone. However, both face mask and prone position were not tolerated. The patient was awake and responsive, and in a last attempt to avoid intubation he was asked to assume an orthopneic (or tripod) position (Fig. 1). Rapidly, after the assumption of tripod position SaO2 improved and patient was kept in the same position with CPAP 10 cmH2O and FiO2 55%. The PaO2/FiO2 ratio increased from 136 to 196 (p < .05) after 3 h and PaO2/PAO2 went from 0.22 to 0.34, showing an actual recovery in terms of O2 effective delivery (Fig. 2). The respiratory rate decreased from 20 to 17 (Table 1) and we were able to lower CPAP to 8 cmH2O and FiO2 to 40%, without changes in SaO2 or hemodynamics. The patient felt more comfortable and able to take some rest in that position compared to the supine position. We continued alternating cycles of tripod and semirecumbent positions for the following 4 days (Fig. 2). Eight days after ICU admission, he was weaned successfully to a conventional O2 Ventimask. SARS-CoV-2 was detected in nasopharyngeal swab specimen until March 28th. On day 10, with a resolution of the pneumonia, he was sent back to a post-COVID ward isolation and then discharged home.

Fig. 2.

Fig. 2

Time course of recorded P/F ratio and paO2/pAO2 ratio during CPAP with alternating cycles of semirecumbent and tripod position. The worst data recorded daily are reported

Table 1.

Respiratory mechanics and hemodynamics in both positions

Supine Tripod p value
PEEP (cmH2O) 10 10 =1
SaO2 (%) 93 99 < 0.05
VT (ml) 370 420 < 0.05
VE (L/min) 5.6 7.2 =0.2
RR (bpm) 20 17 =0.14
PaO2/FiO2 136 196 < 0.05
FiO2 (%) 50 50 =1
A-a(O2) (mmHg) 244 232 < 0.05
PaO2/PAO2 0.22 0.34 =0.89
mBP (mmHg) 90 80 =0.4
HR (bpm) 60 60 =1

Discussion and conclusions

To our knowledge this is the first report of refractory hypoxemia successfully treated with CPAP with helmet and cycles of tripod position. Moreover, this case novelty in our opinion lies also on the peculiar pathology treated, i.e. SARS-CoV-2 pneumonia.

Patients requiring hospitalization usually have hypoxemia due to increased lung permeability, loss of perfusion’s regulation with hyper-perfusion of inflamed lung areas and significant ventilation to perfusion (V/Q) mismatch due to shunt effect, more than to atelectasis [2, 5].

At the beginning, hypoxemia may be compensated by an increase in minute ventilation without marked dyspnea. To some extent in such cases the inspiratory effort is not disproportionate and work of breathing (WOB) tolerable. At this stage, patients are responsive to an increase in FiO2 and to non-invasive ventilation approaches, such as Continuous Positive Airways Pressure (CPAP), aimed at maintaining alveolar patency and improving V/Q matching. However, the transition to more severe clinical patterns of acute respiratory failure is often very rapid. When hypoxemia persist or worsen, the inspiratory load may become excessive, generating too negative swings of intrathoracic pressure and further lung injury [68]. Under such conditions intubation should not be delayed. Clinicians have thus barely a very narrow windows to profit of before shifting to invasive mechanical ventilation when patients are unresponsive to non-invasive approaches.

Hence, changing patients’ position can allow for taking advantage of this “no man’s land” to obtain pulmonary blood flow redistribution, better V/Q matching and increased PaO2/FiO2 ratio.

Actually, body position is not a neutral aspect of patients’ care, as evidenced by an amount of physiological, experimental and clinical studies in different surgical and ICU settings [9, 10]. The modification in position can affect respiratory mechanics by changing resistance and/or compliance of the respiratory system and its lung and chest wall components, and by changing static lung volume and its regional distribution. Mechanical ventilation, either invasive or non-invasive, is commonly delivered in a semi-recumbent supine position, that offer the advantage of increased Functional Residual Capacity (FRC), reduced airways resistance and WOB and improved oxygenation versus the supine [11, 12]. Prone positioning (PP) classically is being used in severe respiratory failure to reopen collapsed lung areas, obtain a more even tidal volume distribution together with a redistribution of pulmonary blood flow [1012], while in SARS-COV-2, PP is indicated mainly because of its effects on blood flow [2, 68].

Under such conditions, the orthopneic or tripod position is a middle way. This posture is often assumed instinctively by individuals experiencing shortness of breath and used in dyspneic patients that sit and lean forward with hands on their knees or on the side of the bed with an over bed table in front to lean on and several pillows on the table to rest on. Patients experience subjective relief of dyspnea, while diaphragmatic function and thoraco-abdominal movements are improved, thus allowing a better V/Q matching [914], as in the present case. Recently, Ding et al. [15] reported the first cases of mild ARDS under non-invasive ventilation successfully treated with PP, without need for intubation. We here suggest that in patients not tolerating to be prone, an alternative may be to keep them in tripod.

In conclusion, to our knowledge, this is the first case that report successful treatment of mild respiratory failure with cycles of tripod position. Although more data are needed to draw definite deductions, this case suggest that in selected SARS-COV-2 patients, a better pulmonary blood flow distribution with improved V/Q matching can be obtained by shifting them in this position, thus avoiding the need for intubation and fasten recovery. We are aware that this represents a single success, thus providing only little evidence on safety and efficacy. But, compared to the risk related to intubation or prone position failure, in this single case, this position, associated to Helmet CPAP, has represented a valid alternative strategy.

Acknowledgements

We want to thank all the great healthcare professionals involved in the ICU COVID-19 Department of “Ospedali Riuniti di Foggia” during this huge emergency.

Abbreviations

COVID- 19

Coronavirus 2019

SARS-CoV-2

Severe Acute Respiratory Syndrome Coronavirus-2

CPAP

Continuous Positive Airways Pressure

PEEP

Positive End Expiratory Pressure

VE

Minute Ventilation

VT

Tidal Volume

RR

Respiratory Rate

V/Q

Ventilation to Perfusion Matching

mBP

Mean Blood pressure

HR

Heart Rate

FiO2

Fraction of Inspired Oxygen

SaO2

Oxygen Saturation

PaO2

Partial Pressure of Oxygen in Arterial Blood

PaCO2

Partial Pressure of Carbon Dioxide in Arterial Blood

PAO2

Partial Pressure of Oxygen in the Alveolar Gas

WBC

White Blood Count

CRP

C Reactive Protein

DIC

Disseminated Intravascular Cascade

IL-6

Interleukin-6

WOB

Work Of Breathing

FRC

Functional Residual Capacity

PP

Prone Positioning

ARDS

Acute Respiratory

ICU

Intensive Care Unit

Authors’ contributions

MR wrote the first draft and designed the work, LM and GC revised the last version. RRC, LPC, MPP, PV, DLB and LT have made substantial contributions to the conception of the manuscript. All authors have read and approved the manuscript and have agreed both to be personally accountable for the author’s own contributions and to ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.

Funding

No founding were received.

Availability of data and materials

Data supporting our findings can be found at gilda.cinnella@unifg.it, the corresponding author.

Ethics approval and consent to participate

Not Applicable.

Consent for publication

The patient gave written consent for his personal and clinical details along with any identifying images to be published in this study.

Competing interests

Authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Rello J, Storti E, Belliato M, Serrano R. Clinical phenotypes of SARS-CoV-2: Implications for clinicians and researchers. Eur Respir J. 2020:2001028. 10.1183/13993003.01028-2020. [DOI] [PMC free article] [PubMed]
  • 2.Marini JJ, Gattinoni L. Management of COVID-19 respiratory distress. JAMA. Published online April 24. 2020. 10.1001/jama.2020.6825. [DOI] [PubMed]
  • 3.Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395:497–506. doi: 10.1016/S0140-6736(20)30183-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020. [e-pub]. 10.1111/jth.14768. [DOI] [PMC free article] [PubMed]
  • 5.Matricardi P, Dal Negro R, Nisini R. The first, comprehensive immunological model of COVID-19: implications for prevention, diagnosis, and public health measures. Preprints. 2020;31(5):454–70. [DOI] [PMC free article] [PubMed]
  • 6.Telias I, Katira BH, Brochard L. Is the prone position helpful during spontaneous breathing in patients with COVID-19? JAMA Published online May. 2020;15. 10.1001/jama.2020.8539. [DOI] [PubMed]
  • 7.Brochard L, Slutsky A, Pesenti A. Mechanical ventilation to minimize progression of lung injury in acute respiratory failure. Am J Respir Crit Care Med. 2017;195(4):438–442. doi: 10.1164/rccm.201605-1081CP. [DOI] [PubMed] [Google Scholar]
  • 8.Elharrar X, Trigui Y, Dols A, et al. Use of prone positioning in nonintubated patients with COVID-19 and hypoxemic acute respiratory failure. JAMA. Published online May 15. 2020. 10.1001/jama.2020.8255. [DOI] [PMC free article] [PubMed]
  • 9.O'Neill S, McCarthy DS. Postural relief of dyspnoea in severe chronic airflow limitation: relationship to respiratory muscle strength. Thorax. 1983;38:595–600. doi: 10.1136/thx.38.8.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Lumb AB, Nunn JF. Respiratory function and ribcage contribution to ventilation in body positions commonly used during anesthesia. Anesth Analg. 1991;73:422–426. doi: 10.1213/00000539-199110000-00010. [DOI] [PubMed] [Google Scholar]
  • 11.Guerin C, Reignier J, Richard JC, et al. Prone positioning in severe acute respiratory distress syndrome. N Engl J Med. 2013;368:2159–2168. doi: 10.1056/NEJMoa1214103. [DOI] [PubMed] [Google Scholar]
  • 12.Milic-Emili J, Henderson JA, Dolovich MB, et al. Regional distribution of inspired gas in the lung. J Appl Physiol. 1966;21:749–759. doi: 10.1152/jappl.1966.21.3.749. [DOI] [PubMed] [Google Scholar]
  • 13.Albert RK, Hubmayr RD. The prone position eliminates compression of the lungs by the heart. Am J Respir Crit Care Med. 2000;161:1660–1665. doi: 10.1164/ajrccm.161.5.9901037. [DOI] [PubMed] [Google Scholar]
  • 14.Gattinoni L, Pesenti A, Carlesso E. Body position changes redistribute lung computed-tomographic density in patients with acute respiratory failure: impact and clinical fallout through the following 20 years. Intensive Care Med. 2013;39:1909–1915. doi: 10.1007/s00134-013-3066-x. [DOI] [PubMed] [Google Scholar]
  • 15.Ding L, Wang L, Ma W, et al. Efficacy and safety of early prone positioning combined with HFNC or NIV in moderate to severe ARDS: a multi-center prospective cohort study. Crit Care. 2020;24:28. doi: 10.1186/s13054-020-2738-5. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Data Availability Statement

Data supporting our findings can be found at gilda.cinnella@unifg.it, the corresponding author.


Articles from BMC Anesthesiology are provided here courtesy of BMC

RESOURCES