key: cord-0885556-ja2enbrv
authors: YAM, Loretta YC; CHEN, Rong Chang; ZHONG, Nan Shan
title: SARS: ventilatory and intensive care
date: 2003-11-14
journal: Respirology
DOI: 10.1046/j.1440-1843.2003.00521.x
sha: 1ae6451f8010b1d53687d1b69dc12af8441f1051
doc_id: 885556
cord_uid: ja2enbrv

Severe acute respiratory syndrome (SARS) is an emerging infection caused by a novel coronavirus. It is characterised by a highly infectious syndrome of fever and respiratory symptoms, and is usually associated with bilateral lung infiltrates. The clinical syndrome of SARS often progresses to varying degrees of respiratory failure, with about 20% of patients requiring intensive care. Despite concern about potential aerosol generation, non‐invasive ventilation (NIV) has been reported to be efficacious in the treatment of SARS‐related ARF without posing infection risks to health care workers (HCW). Spontaneous pneumomediastinum and pneumothorax in SARS is common. The incidence of NIV‐associated barotrauma ranged from 6.6% to 15%. Patients who fail to tolerate NIV or fail NIV with progressive dyspnoea, tachypnoea and hypoxaemia should be intubated and mechanically ventilated. Mortality rates in intensive care units for SARS patients were high: 34–53% at 28 days, when some patients were still being ventilated. Strict adherence to infection control measures including isolation, use of appropriate personal protective equipment and negative pressure environment had been reported to eliminate cross‐infection to HCW.

The initial fever and respiratory symptoms of severe acute respiratory syndrome (SARS) often progress rapidly to acute respiratory failure (ARF) with varying levels of severity. Reported rates of intensive care (ICU) admission vary between 19 to 32%. [1] [2] [3] [4] [5] [6] Early ARF usually peaks by 8 days after symptom onset. 1, 2 But can be delayed with a protracted course. 2 In the ICU, mortality rates similar to or lower than those reported for the acute respiratory distress syndrome (ARDS) 7 have been reported. 1, 5 The following recommendations on the ventilatory and ICU management of SARS are based on published data as well as our local experience. 1 Patients who meet the criteria for acute respiratory distress syndrome (ARDS, defined by PaO 2 /FiO 2 ≤ 200 mmHg) should be cared for in an ICU. Depending on availability, observation in a high dependency (HDU) setting or ICU is indicated in those who meet the criteria for acute lung injury ((ALI), defined by PaO 2 /FiO 2 > 200-300 mmHg, or in those who presented with tachypnoea (respiratory rate > 30/min) and more than 50% progression of chest (bilateral or multilobular) shadows within 48 hours.) 8 2 Patients who develop signs of sepsis, septic shock or multiorgan failure. As SARS is characteristically accompanied by single organ (respiratory) failure 1 multiorgan failure is usually a result of superimposed hospital-acquired bacterial infection.

There is no specific treatment currently available for SARS. Empirical therapy includes broad-spectrum antibiotics and various antiviral agents, with no proven efficacy. 3, 4, 6, 9, 10 Based on the hypothesis that the respiratory failure of SARS is secondary to an immunopathological phenomenon, 10 antiinflammatory agents like corticosteriods have been widely used in Canada, 4 China 5,12-14 and Hong Kong. 3, 6, 9, 10 In particular, short-term intravenous high dose (pulsed) methylprednisolone (500-1000 mg) has been advocated to treat progressive pulmonary infiltrates and hypoxaemia 9, 11, 13 with good response reported. 5, 9, 13, 14 Half of the critically ill patients with SARS might benefit from initial intravenous corticosteroid. 15 Interferon and immunoglobin (including Pentaglobin) 11, 14, 16 have also been used.

Oxygen was required in 50-85% of SARS patients 9, 12, 14 and may be delivered via nasal cannulae at 1-6 L per minute (LPM) or via non-rebreathing masks (NRM) at 8-15 LPM. Patients with continuing deterioration of respiratory status will require ICU care.

Non-invasive ventilation (NIV) is a standard mode of ventilatory assist in early ARF and ARDS due to vari-ous causes. 17, 18 While mortality benefit was not shown, NIV could reduce intubation rate 18 and thus the complications associated with intubation and mechanical ventilation. This may be of particular advantage in SARS, where anti-inflammatory agents could predispose the patients to ventilator-associated pneumonia (VAP).

Despite concern about potential aerosol generation, NIV has been reported to be effective in the treatment of SARS-related ARF without posing infection risks to HCWs. 9, 11, 13, 14 A study reported that NIV was indicated in ALI and early ARDS when desaturation (SaO 2 < 93%) occurred despite oxygen supplementation ( > 3-5 L/m), with persistent tachypnoea ( ≥ 30/min) and progressive deterioration on CXR. 11 Intubation could be avoided in up to two-thirds of cases in a Hong Kong series (unpubl. data, 2003) and in two studies from Guangzhou. 5, 19 The usual contraindications to NIV apply, including disturbed consciousness, uncooperative patient, high aspiration risk and haemodynamic instability.

Conventional mechanical ventilators (pressure support mode), BiPAP® or continuous positive air- 

High risk procedures, alternatives, and precautions Limit opportunities for exposure: Limit aerosol generating procedures & limit number of HCWs present Effective use of time during patient contact How to 'gown' and 'degown' without contamination Emphasis on importance of vigilance and adherence to all infection control precautions Emphasis on importance of monitoring own health Dissemination of information on SARS and other prevailing infections as they evolve

N95 respirator/surgical mask for airborne/droplet precautions Contact precautions: Disposable gloves, gown, cap Eye protection with non-reusable goggles and face-shield Powered air purification respirators (PAPR) may be used when performing high-risk procedures (Figs 1a and 2a) Pens, paper, other personal items and medical records should not be allowed into or removed from the room Immediate removal of grossly contaminated PPE and showering in nearby facility

Conform to CDC recommendations for environmental control of tuberculosis: Minimum 6 air change per hour (ACH). Where feasible, increase to 3 12 ACH or recirculate air through HEPA filter Preferred: Negative pressure isolation rooms with antechambers, with doors closed at all times Equipment should not be shared among patients Alcohol-based hand and equipment disinfectants Gloves, gowns, masks and disposal units should be readily available Careful and frequent cleaning of surfaces with disposable cloths and alcohol-based detergents Use of video camera equipment or windows to monitor patients Transport Avoid patient transport where possible: Balance risks and benefits of investigations which necessitate patient transport

Viral/bacterial filter placed in expiratory port of bag-valve mask Two filters per ventilator: Between expiratory port and the ventilator, and another on the exhalation outlet of the ventilator Closed-system in-line suctioning of endotracheal/tracheostomy tubes (Fig. 2a) Heat and moisture exchanger (HME) preferred to heated humidifier: Careful handling of contaminated HME required (Fig. 2a) Scavenger system for exhalation port of ventilator (e.g. Servo Evac 180, Fig. 2b ): Optional if negative pressure with high air change ( > 12/h) is achieved Preoxygenate patient and temporarily switch off machine when ventilator circuit disconnection required (e.g. change of ventilator tubings, HME, etc.) S33 way pressure (CPAP) machines, preferably with leak compensation capability, may be used to deliver NIV. SARS-related ARF responds readily to low positive pressures of CPAP 4-10 cm H 2 O 5 or inspiratory pressures (IPAP) of < 10 cm H 2 O and expiratory pressures (EPAP) of 4-6 cm water. Higher pressures should be avoided because of the common finding of spontaneous pneumomediastinum and pneumothorax in SARS. 10 The incidence of NIV-associated barotrauma ranged from 6.6% 20 to 15% (unpubl. data, 2003) .

To reduce aerosol generation, exhalation ports that generate round-the-tube airflow (e.g. Whisper-Swivel II, (Respironics, Murrysville, Pennsylvania, USA)) are preferred to those producing jet outflow. A viralbacterial filter interposed between the mask and the exhalation port could further reduce environmental contamination. Strict adherence to infection control measures including isolation, 13 use of appropriate personal protective equipment (PPE) and negative pressure environment 9 had been reported to eliminate cross-infection to healthcare workers. Further details on infection control are shown in Table 1 .

Patients who fail to tolerate NIV or fail NIV with progressive dyspnoea, tachypnoea and hypoxaemia should be intubated and mechanically ventilated. 5, 11 Similar indications apply if NIV had not been used prior to intubation. Both pressure and volume control ventilation have been used to treat SARS-related ARF. 2 Care should be taken to keep the tidal volume low at 5-6 mL/kg, and alveolar (plateau) pressures below 30 cm H 2 O. 2 PEEP levels should be titrated to as low as possible to maintain appropriate oxygenation. Since physical activity or even coughing may result in severe desaturation, sufficient sedation during early mechanical ventilation is useful to eliminate anxiety, thus improving pulmonary oxygenation. 21 A high rate of barotrauma (34%) had been reported, 1 again highlighting the need to avoid excessive volumes and pressures. Permissive hypercapnia resulting from cautious ventilator management necessitated shortterm neuromuscular blockade in 52-70% of ventilated cases. 1,2 Other ventilator modes used include airway pressure release ventilation and high frequency oscillatory ventilation but results have not been reported. 2 Apart from barotrauma, common complications of mechanical ventilation include ventilator-associated pneumonia, acute renal failure, deep vein thrombosis and pulmonary embolism. 2 Low baseline PaO 2 /FiO 2 ratios and high APACHE II scores were the only predictors for protracted ARDS and death in one study. 2 ICU mortality rates were high: 34-53% at 28 days, when some patients were still being ventilated. 1,2 To improve survival, research is required to identify early all SARS patients who may progress to severe ARDS and to develop effective treatment.

Meticulous infection control measures (Table 1) are mandatory in the care of ventilated SARS patients in ICU, where HCW are exposed to high risk procedures like bag-mask ventilation, NIV, endotracheal intuba- tion, actual or potential circuit disconnections, suctioning, tracheostomy and bronchoscopy with or without bronchoalveolar lavage. The duration of manual ventilation during resuscitation procedures should be reduced to a minimum. Endotracheal intubation should be performed by the most skilled person available 22 using rapid sequence induction: risk of aerosol generation is lowest when the patient is paralysed. All special precautions for ICU patients must be complied with. Contrary to recommendations to avoid NIV and nebulised therapy, 22 NIV has not been reported to be associated with increased infection risk for HCW, and doubts have been raised about the role of nebulised treatment on the spread of SARS within the hospital. 24 On the other hand, it is always prudent to limit opportunities for HCW exposure and to perform aerosol generating procedures in an airborne isolation environment. 25 In addition to ensuring the safety of HCWs, timely psychological support is critical to maintain staff morale. 2 The above strategies had been effective in preventing infection in ICU HCWs in hospitals in Singapore 2 and Hong Kong, and in the latter case over 80 HCWs exposed to NIV and mechanical ventilation of SARS patients were proved to be serologically negative for SARS-CoV after the outbreak (unpubl. data, 2003). for connection to exhalation port of ventilator. The Servo-Evac 180 consists of a connection to the ventilator's expiratory port (curved flexitube) which empties expired air into a Evac Bag, which has a one-way valve through which expired gas can be removed via an evacuation hose (white tube) connected to a suction source. The straight flexitube is open to the atmosphere to ensure the patient is not subjected to undue negative pressure or excessive resistance in case the suction sources is interrupted. 

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