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      What we do when a COVID-19 patient needs an operation: operating room preparation and guidance

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      , MBBS, MMed, FAMS 1 , 2 , , , MBBS, MMed, FANZCA, EDIC 1 , , MBBS, MMed 1 , , MBBS, FRCA 1
      Canadian Journal of Anaesthesia
      Springer International Publishing

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          Abstract

          To the Editor, We read with interest the recent review in the Journal by Wax and Christian1 on coronavirus disease 2019 (COVID-19). The first case of COVID-19 in Singapore was confirmed on 23 January 2020.2 In the week of February 13–19, the World Health Organization reported that Singapore had more cases of COVID-19 than any other country outside of mainland China.3 We wish to share the protocol that we use in our hospital in preparing an operating room (OR) for confirmed or suspected COVID-19 patients coming for surgery. An OR with a negative pressure environment located at a corner of the operating complex, and with a separate access, is designated for all confirmed (or suspected) COVID-19 cases. The OR actually consists of five interconnected rooms, of which only the ante room and anesthesia induction rooms have negative atmospheric pressures. The OR proper, preparation, and scrub rooms all have positive pressures (eFig. 1 in the Electronic Supplementary Material [ESM]). Understanding the airflow within the OR is crucial to minimizing the risk of infection. The same OR and the same anesthesia machine will only be used for COVID-19 cases for the duration of the epidemic. An additional heat and moisture exchanger (HME) filter is placed on the expiratory limb of the circuit. Both HME filters and the soda lime are changed after each case. The anesthetic drug trolley is kept in the induction room. Before the start of each operation, the anesthesiologist puts all the drugs and equipment required for the procedure onto a tray to avoid handling of the drug trolley during the case. Nevertheless, if there is a need for additional drugs, hand hygiene and glove changing are performed before entering the induction room and handling the drug trolley. A fully stocked airway trolley is also placed in the induction room. As far as possible, disposable airway equipment is used. The airway should be secured using the method with the highest chance of first-time success to avoid repeated instrumentation of the airway, including using a video-laryngoscope.4 Equipment in limited supply, such as bispectral index monitors or infusion pumps, may be requested but need to be thoroughly wiped down after use. The Figure  details the roles and responsibilities of each OR team member. Hospital security is responsible for clearing the route from the ward or intensive care unit (ICU) to the OR, including the elevators. The transfer from the ward to the OR will be done by the ward nurses in full personal protective equipment (PPE) including a well-fitting N95 mask, goggles or face shield, splash-resistant gown, and boot covers. For patients coming from the ICU, a dedicated transport ventilator is used. To avoid aerosolization, the gas flow is turned off and the endotracheal tube clamped with forceps during switching of ventilators. The ICU personnel wear full PPE with a powered air-purifying respirator (PAPR) for the transfer. Figure Complete operating room workflow for a coronavirus disease 2019 (COVID-19) case. CD = controlled drugs; ICU = intensive care unit; NM = nurse manager; OR = operating room; PAPR = powered air-purifying respirator; PC = personal computer; PPE = personal protection equipment; pre-op = preoperative In the induction room, a PAPR is worn during induction and reversal of anesthesia for all personnel within 2 m of the patient. For operative airway procedures such as tracheostomy, all staff keep their PAPR on throughout the procedure. For other procedures, regional anesthesia is preferable, but if general anesthesia is required, the principles of management are similar to those previously published.1,4 During the procedure, a runner is stationed outside the OR if additional drugs or equipment are needed. These are placed onto a trolley that will be left in the ante room for the OR team to retrieve. This same process in reverse is used to send out specimens such as arterial blood gas samples and frozen section specimens. The runner wears PPE when entering the ante room. Personnel exiting the OR discard their used gowns and gloves in the ante room and perform hand hygiene before leaving the ante room (ESM, eFig. 2). Any PAPR will be removed outside the ante room. Patients who do not require ICU care postoperatively are fully recovered in the OR itself. When the patient is ready for discharge, the route to the isolation ward or ICU is again cleared by security. A minimum of one hour is planned between cases to allow OR staff to send the patient back to the ward, conduct through decontamination of all surfaces, screens, keyboard, cables, monitors, and anesthesia machine. All unused items on the drug tray and airway trolley should be assumed to be contaminated and discarded. All staff have to shower before resuming their regular duties. As an added precaution, after confirmed COVID-19 cases, a hydrogen peroxide vaporizer will be used to decontaminate the OR. In summary, as healthcare workers are at increased risk of coronavirus infection, a comprehensive and robust infection control workflow has been put into place.5 Electronic supplementary material Below is the link to the electronic supplementary material. Supplementary material 1 (PDF 604 kb)

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          Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus–Infected Pneumonia in Wuhan, China

          In December 2019, novel coronavirus (2019-nCoV)-infected pneumonia (NCIP) occurred in Wuhan, China. The number of cases has increased rapidly but information on the clinical characteristics of affected patients is limited.
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            Practical recommendations for critical care and anesthesiology teams caring for novel coronavirus (2019-nCoV) patients

            A global health emergency has been declared by the World Health Organization as the 2019-nCoV outbreak spreads across the world, with confirmed patients in Canada. Patients infected with 2019-nCoV are at risk for developing respiratory failure and requiring admission to critical care units. While providing optimal treatment for these patients, careful execution of infection control measures is necessary to prevent nosocomial transmission to other patients and to healthcare workers providing care. Although the exact mechanisms of transmission are currently unclear, human-to-human transmission can occur, and the risk of airborne spread during aerosol-generating medical procedures remains a concern in specific circumstances. This paper summarizes important considerations regarding patient screening, environmental controls, personal protective equipment, resuscitation measures (including intubation), and critical care unit operations planning as we prepare for the possibility of new imported cases or local outbreaks of 2019-nCoV. Although understanding of the 2019-nCoV virus is evolving, lessons learned from prior infectious disease challenges such as Severe Acute Respiratory Syndrome will hopefully improve our state of readiness regardless of the number of cases we eventually manage in Canada.
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              Outbreak of a new coronavirus: what anaesthetists should know

              In December 2019, an outbreak of pneumonia of unknown origin developed in Wuhan of Hubei Province, China. 1 By January 7, 2020, Chinese scientists confirmed that the outbreak was caused by a novel coronavirus, initially referred to as the 2019-nCoV, 2 and recently renamed as severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2), and the disease is now termed coronavirus disease 2019 (COVID-19) by the WHO. As of February 20, 2020, more than 75,748 confirmed cases of COVID-19 have been reported in 28 countries (including China) and international conveyance (cruise ship in the Japanese territorial waters), with approximately 99% of cases occurring in mainland China. 3 The WHO declared a public health emergency of international concern (PHEIC) on January 30, 2020 in response to the rapid growth of the outbreak and reports of human-to-human transmission in several countries. 3 Here, we summarise how key events unfolded, review the current understanding of COVID-19, contrast the outbreak of COVID-19 with the experience with severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), and discuss how anaesthetists should prepare themselves in view of this outbreak. Tracking the course of the outbreak The evolving story of the COVID-19 outbreak has advanced over a remarkably short time frame (Fig 1 ). On December 31, 2019, the Wuhan Municipal Health Commission reported a cluster of pneumonia of unknown origin, all linked to the Huanan Seafood Wholesale Market. This market harboured a variety of live and deceased exotic wildlife, including live bamboo rats, palm civets, badgers, and wolf cubs. It is notable that a quarter of the initially reported 27 pneumonia cases presented with severe disease.4, 5 Within days, the cause of the pneumonia was identified as a novel coronavirus (2019-nCoV). 2 On January 19, 2020 the WHO issued a warning that the virus may have the ability to spread from human to human. 3 Figure 1 Timeline of the outbreak of 2019-nCoV/coronavirus disease 2019 (COVID-19). Figure 1 Wuhan is a major transportation hub within China with a population of 11 million. On a typical day, approximately 3500 people take flights to other countries from Wuhan, and the number increases with holidays and the Chinese Lunar New Year. Within 1 month, the number of confirmed COVID-19 cases rose to more than 9000, surpassing the number of SARS and MERS cases reported to date. Similarly, global fears escalated as cases spread to other countries. Extensive control measures were put into place, starting with massive decontamination efforts and, ultimately, closure of the Huanan Seafood Wholesale Market, banning the trade of wildlife and poultry in wet markets, contact tracing of cases, exit screening at airports, lockdown and quarantine measures that progressed to include adjacent cities (an estimated 50–60 million people affected), school closures, extension of the Lunar New Year holiday, prohibition of mass gatherings, and building of two new hospitals (1000 and 1600 beds) to care for infected individuals. Other nations instituted airport screening, travel bans, and evacuating citizens from Hubei Province and quarantining them through the incubation period. 6 Despite these measures, the case counts continued to increase in the outbreak epicenter, and countries with imported cases reported clusters of human-to-human transmission. On January 30, 2020, the WHO declared a PHEIC, calling for intensified international collaborative efforts to halt the outbreak. 3 Although Chinese authorities have heavily restricted movement from Wuhan, this austere measure came at the same time as the Spring Festival, a time when the number of outbound travellers from Wuhan is estimated to be more than 15 million. What is 2019-nCoV/COVID-19? The 2019-nCoV or SARS-CoV-2 is an enveloped RNA virus that belongs to the Coronaviridae, a family of viruses that can infect humans and several animal species. To date, seven human coronaviruses have been identified (HCoV-229E, HCoV-NL63, HCoV-OC43, HCoV-HKU1, SARS-CoV, MERS-CoV, and SARS-CoV-2). 7 The SARS-CoV-2 belongs to the subgenus Sarbecovirus and most closely resembles a bat coronavirus, with which it shares 96.2% genetic sequence homology.2, 8, 9 The current belief is that COVID-19 was introduced into humans through an as yet unidentified intermediary animal, and it has since propagated through human-to-human spread. Human-to-human transmission occurs primarily through respiratory droplets that travel up to 2 m and may enter the respiratory tract of individuals within range or contaminated surfaces, leading to infection through contact transmission. 10 The average incubation period is 5 days, but it ranges from 1 to 14 days.10, 11 The basic reproductive number (the number of cases one infected individual generates), R 0, is estimated to be 2.68 (95% confidence interval: 2.47–2.86). 12 Whilst asymptomatic transmission (during the incubation period, before onset of symptoms in infected individuals) has been suggested, it remains controversial and currently does not appear to be a major factor for infection transmission. 10 Infections in humans result in a spectrum of clinical disease, from mild upper respiratory tract infection, mostly commonly characterised by fever (82%) and cough (81%), to severe acute respiratory distress syndrome (ARDS) and sepsis. The median age of infected individuals is between 49 and 56 yr.1, 13 Children are rarely diagnosed with 2019-nCoV, a phenomenon that has not yet been explained. Characterisation of the first 99 cases of 2019-nCoV within Wuhan demonstrated that 33% had severe illness, with 17% developing ARDS, 4% requiring mechanical ventilation, and 4% having sepsis. 13 The case fatality rate is currently estimated at 2% based on the confirmed cases reported for the ongoing outbreak. 3 However, as mild and subclinical infections are currently under-reported, the true case fatality is likely lower than this. 14 People with co-morbidities, such as diabetes mellitus and cardiovascular disease, appear to be at higher risk for death.1, 13 Comparison with the SARS and MERS outbreak Several similarities and differences exist amongst the SARS, MERS, and 2019-nCoV viruses (Table 1 ). All three coronaviruses were introduced into humans from wild animals (masked palm civets in SARS, camel in MERS, and unclear intermediary for 2019-nCoV).15, 16 All three can cause severe respiratory distress symptoms and death, although fatality rates range considerably, with MERS being the most lethal (case fatality rate: 35%). 16 There have been no further documented cases of SARS since July 2003, but MERS continues to be reported sporadically, generally as a result of animal-to-human contact or transmission in healthcare facilities and within families. Compared with SARS, with which it shares nearly 70% genetic homology, 2019-nCoV appears to be more transmissible (higher R 0) but less fatal. 13 Table 1 Comparison of the outbreak from severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), and 2019-nCov/coronavirus disease 2019 (COVID-19) respiratory syndrome. CoV, coronavirus. Table 1 SARS MERS COVID-19 Timeline November 2002 to July 2003 June 2012 to present December 2019 to present Location of first detection Guangdong, China Jeddah, Saudi Arabia Wuhan, China Animal origin Civet Camel Non-aquatic animal (?) Confirmed cases 8096 2494 12 404 Fatality 744 (10%) 858 (37%) 259 (∼2%) Global impact 26 countries 27 countries 26 countries Date of virus identification April 2003 October 2012 January 7, 2020 The current outbreak of COVID-19 has benefited from several advancements that have resulted in a different experience from the SARS outbreak in 2002–3. Improved reporting, transparency, and communication Health officials in China exhibited a much higher degree of transparency early in this outbreak and were quicker to notify the WHO after they discovered the cluster of pneumonia of unknown origin. The identification of the aetiological virus occurred promptly in early January, and the full genome sequence data were shared on the Global Initiative on Sharing All Influenza Data platform. 8 The update International Health Regulations (2005) was signed 2 yr after the SARS outbreak by 194 member states, with legal binding on the protection of all people of the world from international spread of disease. 17 Global surveillance and alerting systems developed since SARS enabled rapid dissemination of information on the emerging outbreak. Public health officials and the WHO have held numerous press conferences to inform the public on important developments. Scientific papers have been published with rapid peer review to share the clinical and epidemiological characteristics of the virus within the medical community. Technological advancements During the SARS outbreak, the aetiological virus was identified 5 months after the outbreak began. In contrast, the virus and the genomic characteristic were identified within 2 weeks of the discovery of the COVID-19 outbreak. 8 This is very significant, as this information allows rapid development of real-time polymerase chain reaction diagnostic tests specific to SARS-CoV-2. 18 This has allowed some countries to have diagnostic testing available before the first case arrived in their countries—a significant step in curbing the spread of the virus globally. Early identification of the full genome also aids in vaccine development. Companies, such as Tencent (Shenzhen, China) and Alibaba (Hangzhou, China), provide databases running in real time to release the latest statistics needed for contact tracing and for management of essential supplies (such as masks and gowns). Technology has also accelerated information sharing through social media and the internet, which was still in its infancy during the SARS outbreak. Infection prevention and control and public health infrastructure expansion. Since the SARS outbreak, the WHO has declared five PHEIC. As a result of these events, significant investments have been made into public health and infection prevention programmes in many jurisdictions. Public health programmes coordinate rapid case finding, tracing of contacts of cases, and isolation measures to mitigate spread, and guide decision-making on broad public health measures, such as social distancing when required. Hospital infection prevention and control programmes aid with case identification through screening and testing, and they execute isolation infection prevention measures to ensure healthcare settings are safe from infection transmission. The latter is of utmost importance, as both the SARS and MERS viruses have disproportionately infected healthcare providers and healthcare settings have been hotspots of infection transmission. What anaesthetists need to know in response to this outbreak During the SARS outbreak, 21% of the infected individuals globally were healthcare workers. 15 In Canada, a final count of 251 cases of SARS was confirmed; 43% of them were healthcare workers, the majority were from Toronto. 15 Concerns were raised about infections in healthcare workers despite apparently appropriate personal protective equipment (PPE). Analysis of this experience uncovered several important lessons. 19 First, the protection of healthcare workers is not just about PPE; it encompasses all principles of infection prevention and control. 20 Whilst the initial focus for protecting anaesthesiologists or personnel involved in aerosol-generating medical procedures (tracheal intubation, non-invasive ventilation, tracheotomy, cardiopulmonary resuscitation, manual ventilation before intubation, and bronchoscopy) was on the need for more stringent PPE, such as powered air-purifying respirators or double gloves during the SARS outbreak, further investigation did not support a risk of transmission with tracheal intubation if appropriate precautions and more standard PPE were used.21, 22 In areas, such as the emergency department or ICU where SARS patients were managed, there were ‘uncontrolled situations characterized by multiple opportunities for extensive contamination and staff exposure prior to the intubation event’. 21 Healthcare workers were exposed to risk of infection before PPE was used. It reflects the importance of triage, early recognition, and prompt isolation for suspected cases of infected patients. 20 Second, a post-SARS investigation interviewing healthcare workers involved in the intubation of SARS patients in Toronto highlighted non-compliance or sub-optimal adherence to the use of PPE. 23 Although much is unknown about the 2019-nCoV, it is believed to spread from person to person amongst close contact via respiratory droplets and contact transmission. Strict adherence to the use of PPE, including procedure mask, eye protection, gown, and gloves, is highly effective in limiting droplet and contact transmission. 21 The current WHO and Centers for Disease Control and Prevention guidance for the protection of personnel during aerosol-generating medical procedures in patients with confirmed/suspected 2019-nCoV centres around principles of clear communication, minimising personnel in the room during the procedure, appropriate use of PPE, and avoidance of procedures that generate high amounts of aerosols. Some considerations are provided as follows to help prepare for airway management of confirmed/suspected COVID-19 patients.20, 24, 25 These suggestions are by no means comprehensive. Hospitals should develop local plans for aerosol-generating medical procedures in suspected/confirmed COVID-19 patients using a collaborative approach that engages anaesthesiologists, intensivists, emergency medicine physicians, respiratory therapists, resuscitation team members, infection prevention and control, occupational health and safety specialists, and environmental services staff. Preparing the patient and procedure room Transfer of a suspected or infected COVID-19 patient to the room for aerosol-generating medical procedures requires planning. Considerations include: (i) The room should be adequately ventilated; for aerosol-generating medical procedures performed outside the operating theatre, a negative pressure/airborne isolation room with minimum 12 air changes h−1 is preferred. (ii) The patient should wear a face mask during transport to the procedure room. (iii) The staff involved in the care of the patient should don PPE as required by their hospital's policy for management of COVID-19. (iv) Hand hygiene must be performed by staff before and after all patient contact, particularly before putting on and after removing PPE. (v) The number of individual staff members involved in the resuscitation should be kept to a minimum with no or minimal exchange of staff for the duration of the case, if possible. PPE considerations (i) Specific PPE components selected for aerosol-generating medical procedures may vary slightly by hospitals. However, the underlying principles are the same: to protect the healthcare provider from inhalation of and contact with aerosols and droplets that may be generated during the procedure. PPE components that may be used to accomplish this level of protection include: (a) A particulate respirator (US National Institute for Occupational Safety and Health-certified N95, EU standard FFP2, or equivalent); all healthcare workers should have an updated respirator fit test; (b) Eye protection, through the use of goggles or a disposable face shield; (c) Gown with fluid resistance; and (d) Gloves. (ii) Any PPE component that becomes heavily soiled during aerosol-generating medical procedures should be replaced immediately. (iii) Careful attention must be paid to donning and doffing of PPE to avoid potential exposure and self-contamination, which is highest during removal of PPE. All healthcare workers attending to aerosol-generating medical procedures should be trained and comfortable with PPE use, including safe donning and doffing. (iv) After removing protective equipment, the healthcare worker should avoid touching the hair or face before cleaning hands. (v) PPE should be disposed of carefully in a touch-free disposal or laundering bin. Minimisation of the aerosol generation To minimise the aerosols generated during airway instrumentation, some factors to consider include the following: (i) Airway management should be reserved for the most experienced anaesthetist, if possible. (ii) A high-efficiency hydrophobic filter interposed between face mask and breathing circuit or between face mask and airway bag can be used, if available. (iii) A thorough preoxygenation with 100% oxygen and rapid sequence induction (RSI) should be considered to avoid manual ventilation of the patient, which can result in aerosolisation of virus from airways. (iv) RSI may need to be modified if the patient has a very high alveolar–arterial oxygen gradient, is unable to tolerate 30 s of apnoea, or has a contraindication to succinylcholine. If manual ventilation is anticipated, small tidal volumes should be applied. (v) Awake fibreoptic intubation should be avoided unless specifically indicated, as the atomised local anaesthetic and the coughing episode during anaesthetising of the airway can aerosolise the virus. Consider the use of a videolaryngoscopy. (vi) Tracheal intubation rather than the use of laryngeal mask is favoured. (vii) In managing patients with respiratory distress from coronavirus infection outside the operating theatre, non-invasive ventilation should be avoided, if possible, to prevent generation of aerosol of virus in the room, and early intubation should be considered in a rapidly deteriorating patient. Whilst resuscitating the critically ill patient, chest compressions should be held during intubation to avoid exposing the face of the intubating clinician to aerosols, and neuromuscular blockers should be considered before intubation, if possible. Conclusions The current outbreak of COVID-19 has rapidly expanded over a short time. Confirmed cases continue to increase despite austere measures applied by the Chinese government and public health officials around the world. Up to one-third of affected patients may require a higher level of care in hospital, including mechanical ventilation in the early report. Anaesthesiologists are experts in airway management and will be on the frontlines of managing critically ill patients. Learning from previous experiences with SARS and understanding the current epidemiological factors of the COVID-19, anaesthesiologists are much better prepared to protect themselves during aerosol-generating medical procedures. A good knowledge of infection prevention and control, vigilance in protective measures, strict adhesion of donning and doffing of PPE, and preparedness for the care of infected patients are of utmost importance. Authors' contributions Writing/editing of paper: all authors. Approval: all authors. Declarations of interest The authors declare that they have no conflicts of interest.
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                Author and article information

                Contributors
                lian_kah_ti@nuhs.edu.sg
                Journal
                Can J Anaesth
                Can J Anaesth
                Canadian Journal of Anaesthesia
                Springer International Publishing (Cham )
                0832-610X
                1496-8975
                6 March 2020
                : 1-3
                Affiliations
                [1 ]GRID grid.410759.e, ISNI 0000 0004 0451 6143, Department of Anaesthesia, , National University Health System, ; Singapore, Singapore
                [2 ]GRID grid.4280.e, ISNI 0000 0001 2180 6431, Department of Anaesthesia, Yong Loo Lin School of Medicine, , National University of Singapore, ; Singapore, Singapore
                Article
                1617
                10.1007/s12630-020-01617-4
                7090746
                32144591
                a49b4355-2f7e-483e-8f3e-1aca74041098
                © Canadian Anesthesiologists' Society 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 1 March 2020
                : 3 March 2020
                : 3 March 2020
                Categories
                Correspondence

                Anesthesiology & Pain management
                Anesthesiology & Pain management

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