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      Kicking on while it’s still kicking off – getting surgery and anaesthesia restarted after COVID‐19

      editorial
      1 , 2 , , 3 , 4
      Anaesthesia
      John Wiley and Sons Inc.
      COVID‐19, peri‐operative, surgery

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          Abstract

          The UK National Health Service (NHS) has risen to the challenge posed by COVID‐19 through herculean efforts to expand capacity. This has included doubling or trebling intensive care (ICU) capacity within hospitals, augmenting this with Nightingale hospitals, cancelling all non‐emergency surgery and redeploying staff and equipment to focus on a single disease. At the same time, government and population efforts have – through social distancing then lockdown – successfully flattened the epidemic curve and so reduced demand. Together, these actions have enabled treatment of all those needing hospital care for COVID‐19 and avoided the unfettered increase in mortality that would have accompanied an overwhelmed healthcare service. However, this has been achieved ‘by the skin of our teeth’ and until very recently, the threat of insufficient ICU beds [1], ventilators [2], and the need for triage [3, 4] were all anticipated: a few hospitals were overcome by the surge of critically ill patents [5, 6]. Now, political and social thoughts and actions are turning to loosening lockdown and determining what ‘post‐pandemic normality’ will look like. Here, we discuss the prospects and challenges of ‘planned surgery’ – both time‐critical and wholly elective procedures. Elective activity While managing the pandemic, many people have been disadvantaged by reduced routine NHS activity. Hospital admissions and emergency department attendances are down by > 30% [7, 8]. Increases in mortality are not entirely explained by COVID‐19 [9], and concern exists that some are not seeking or receiving the hospital care they need. The issue, particularly cancer patients awaiting treatment, is rightly high on the agenda of the NHS, professional bodies and the public [7, 10, 11]. The NHS has described us entering the ‘second phase of the pandemic’, directed us to restart urgent work [7] and has declared itself ‘open for business’ [12]. Having weathered the COVID‐19 storm, we are now being asked to assess the damage done, pick up the pieces and rebuild. However, this storm will rage for many months. Flattening the epidemic curve does not reduce the total number of cases but spread their burden over a longer period of time; this is ‘delay’ not ‘mitigation’ [13]. Increased pandemic‐related hospital activity may last throughout 2020 and the secondary healthcare system impacts will likely be evident for several years. Over the next few months we need to do a number of things at the same time: continue to manage the increased ICU activity associated with COVID‐19; make hospitals safe for patients who have, may have and do not have COVID‐19; ensure that all patients are treated fairly in terms of access and safety; and restore staff and services to as many pre‐pandemic pathways as possible. Concurrently, the lockdown will be loosened, though a level‐4 national incident will remain [7, 14]. Disease transmission precautions will continue including social distancing within hospitals, including between ward beds (significantly decreasing bed capacity), enhanced infection control practices and ongoing use of personal protective equipment (PPE; dramatically slowing processes), all while staff will continue to fall sick (reducing staff numbers). These are major challenges, which we explore here. Protecting patients and staff While some medical care can be undertaken remotely, anaesthesia and surgery are physical acts and adherence to social distancing is impossible. This exposes staff and patients to the risk of infection from each other, so it will be necessary to attempt to create COVID‐19‐free and COVID‐19‐affected pathways [7, 15]. Ideally, pathways would keep staff in cohorts that either manage COVID‐19 and emergency work, or elective non‐COVID‐19 work. There are challenges in ensuring COVID‐free staff (see below) and whether staff will be willing to be in a cohort undertaking only ‘higher risk care’ for prolonged periods of time is uncertain. Equally important, emerging evidence points towards poor outcomes and high mortality from even relatively minor surgery undertaken when a patient is SARS‐CoV‐2 infected [15, 16]. Meticulous pre‐operative patient isolation for 14 days combined with antigen testing, that is, detecting viral RNA with reverse transcriptase polymerase chain reaction (RT‐PCR) tests and ensuring no symptoms or pyrexia in the last week is recommended by many, and aims to deliver a patient who is not infected or incubating COVID‐19. However, the 95% confidence interval for the upper limit of the incubation period can stretch to 2 weeks [17]. Virus can be shed by for up to 5 days before symptoms [18] and by asymptomatic patients [19]. The false negative rate for RT‐PCR tests ranges between 3% and 40%, being dependent on disease time‐course, the individual’s virus shedding characteristics and testing technique [20, 21]. Although respiratory viral loads (and probably disease transmission) generally peak within the first week of illness [22] and although quantitative viral shedding probably correlates with disease severity [23], this is not clear‐cut [22] and respiratory viral shedding can persist for 2 weeks after mild disease [22, 23, 24], beyond a month during severe disease [24, 25] and may even stop and restart [22]. The prolonged, variable incubation period, the potential to infect while asymptomatic, unreliable antigen tests and extended duration of viral shedding mean that isolation and screening based on symptoms and antigen tests, while reassuring and pragmatic, will not guarantee a COVID‐19‐free patient. Some are using pre‐operative computerised tomography (CT) chest scanning as part of screening for COVID‐19. However, chest CTs are normal in 39–56% of patients in the early stages of COVID‐19 [26, 27] and in 20% of symptomatic hospitalised patients [26, 27]. Further, CT abnormalities when present are heterogeneous and non‐specific [26, 27]. A normal chest CT, especially one done more than 48 h previously, does not exclude coronavirus infection. The surgical Colleges and Royal College of Radiologists have recently revised their previous advice to undertake CT scanning for major surgery and no longer recommended it as a routine pre‐operative test [28, 29]. Antibody testing too could have value in identifying patients and staff who have had and recovered from COVID‐19. It is not yet widely available and antibody responses appear inconsistent and possibly transient (https://www.medrxiv.org/content/10.1101/2020.04.15.20066407v1.full.pdf). Evaluation of antibody responses and detection methods suggest detectable antibody responses take approximately 10 days to develop (https://www.medrxiv.org/content/10.1101/2020.04.25.20074856v1) and that a method that detects both IgM and IgG antibodies is likely preferable [22]. Laboratory‐based testing using an enzyme‐linked immunosorbent assay (ELISA) has a sensitivity of approximately 85%, but putative home‐testing point of care testing techniques using lateral flow immuno‐assay (LFIA), have rather disappointing sensitivities as low as 55% and imperfect specificity (false positive rate approximately 5%). Patient isolation for 2 weeks and antigen testing within 48 h of surgery creates practical problems for peri‐operative preparation. Attendance for blood tests and other pre‐operative investigations may need to be undertaken before the 2‐week isolation starts. Cross‐matching of blood may be a particular challenge as may ensuring sufficient and safe transfusion supplies [30]. The value of the above tests and whether risk reduction approaches are sufficient, is greatly dependent on the prevalence of SARS‐CoV‐2 in the community and therefore the risk of expected infection, that is, the pre‐test probability of a positive result. This is currently unknown and almost certainly varies widely between regions but is perhaps where large‐scale antigen and antibody testing may have their greatest benefit, through determining population prevalence of disease and convalescence in the community and among hospital staff. Proportionate PPE For the time being then, we cannot be certain whether patients presenting for planned surgery or staff treating them are infected. The risk is likely low in most settings, but many will correctly assert that it cannot be zero for some time. Current PPE strategies in the UK appear to be protecting anaesthetists and intensivists from the worst effects of COVID‐19, with no deaths reported in those working in anaesthesia or intensive care [31]. The question then arises of which infection prevention and control practices should be adopted in theatres undertaking planned surgery and when should current transmission prevention practices be relaxed. If the prevalence of the virus in the community is very low, the patient has been isolated and screened, and the teams similarly screened and perhaps isolated, then it is reasonable to assume a low risk of viral transmission. However, how low must the prevalence be before all staff will be prepared to accept lower levels or abandonment of PPE? Flattening the curve means disease prevalence will be sustained for many months and loosening lockdown may increase this: the transition back to pre‐pandemic behaviour will take time. Of course, maintaining widespread transmission control precautions will reduce theatre efficiency and increase demand on the limited supplies of PPE. This demand will be exacerbated by restarting non‐medical industries that use PPE as an alternative to social distancing [14] and if there is widespread community use of facemasks [32]. As PPE use will be prioritised for the management of known COVID‐19 patients elsewhere, any inability to identify low‐risk patients accurately and scale down PPE use may be a further barrier to increasing planned surgery activity. Bringing back staff and resources Increasing critical care capacity to cope with the COVID‐19 surge has leant disproportionately on many key elements of the planned surgery pathway. Anaesthetists and some surgeons, theatre teams, operating theatres and recovery rooms, anaesthetic machines and target‐controlled infusion pumps have all been re‐purposed as ICU resources. Repatriation of these key elements to their proper places in peri‐operative pathways is a prerequisite to any return to pre‐pandemic levels of planned surgery. However, repatriation will not be easy as it will be necessary to maintain critical care capacity above pre‐pandemic levels for some months. Temporary ICUs in locations within surgical pathways need to be emptied and relocated: new space must be found. Anaesthetists and operating theatre staff must return to theatre duties but will need to be replaced or additional staff employed, if they can be found. Extra ventilators suitable for complex COVID‐19 patients will be needed. Demand for drugs including opioids, propofol, neuromuscular blocking drugs and vasopressors will increase but supplies are already critically low [33, 34]. Above all, there will need to be an understanding that although equipment such as anaesthetic machines and syringe drivers can be decontaminated, serviced and pressed back into service within hours, human beings will need more care if they are to continue to work effectively, efficiently and safely. Increased hours, disruptive shift patterns, working outside of specialty ‘comfort zones’, missed leave and moral injury will all combine to produce a workforce that cannot be driven straight back to full‐time work in peri‐operative pathways [35]. There will be a pressing need for rest, recuperation and therapy without which bold plans for dramatic increases in the delivery of planned surgery will founder [33]. Prioritisation of surgery The combination of reduced availability of anaesthetic and theatre staff, slowed theatre processes, supply chain factors and reduced hospital bed capacity are likely to severely limit planned surgical capacity for many months. Displacement of surgical or other activity to alternative locations such as independent sector hospitals, mobile facilities and Nightingale hospitals may help, but these mainly provide space. The staff and resources required to service these areas are generally the same that are now servicing the NHS and can be only in one place at a time. This all points to a need for clear and fair prioritisation of surgery. Surgical colleges have already published advice on this, creating five levels of surgical priority (1, 1a and 2‐4) ranging from ‘operation needed within 24 h’ to ‘can be delayed for more than 3 months’ [36]. This guidance is well thought out, detailed and can be used to create a roadmap for different services and for communicating realistic expectations to patients. However, waiting for 3 months may underestimate the reality, and non‐urgent surgery may be delayed much longer. Ethics Ethical considerations may return to prominence. The move from a health service focused on one single disease to one that continues that challenge while also addressing all the other health needs of the population may be even harder than that the crisis phase that preceded it. There may be more urgent or time‐dependent surgery than the new system can cope with, through a backlog of untreated pathology and lack of staff, space, beds or kit. The needs of all patients must be balanced: not just COVID‐19 positive vs. COVID‐19 unaffected, but also surgical and non‐surgical, physical and mental health. The need for careful adoption of ethical frameworks, fair allocation of resources and even triage may not yet be something with which we can dispense during this pandemic. Conclusions A superficial appraisal of the situation regarding resumption of planned surgery reveals that we have all we need: patients who need surgery and surgeons who can perform it. This may understandably foster calls for swift action to restore surgical normality. However, these are the only intact parts of complex surgical pathways. All other elements have been repurposed, relocated, exhausted, overused or in other ways adversely affected. Restoration of these pathways will be a large part but not the totality of a return to planned surgery. Perhaps even more important will be the creation of new pathways that work much more effectively and efficiently in a world in which we have to co‐exist with SARS‐CoV‐2. Those who create, test, develop and implement these pathways will need investment and support if planned surgery is to return to the level we would all wish. It is right and proper that we rise to this new challenge. To do so, anaesthetists, peri‐operative physicians, surgeons and all other team members will need to use all of their vision, skills, experience and compassion if we are going to kick on while it’s still kicking off.

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          Most cited references21

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          Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

          Summary Background Since December, 2019, Wuhan, China, has experienced an outbreak of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Epidemiological and clinical characteristics of patients with COVID-19 have been reported but risk factors for mortality and a detailed clinical course of illness, including viral shedding, have not been well described. Methods In this retrospective, multicentre cohort study, we included all adult inpatients (≥18 years old) with laboratory-confirmed COVID-19 from Jinyintan Hospital and Wuhan Pulmonary Hospital (Wuhan, China) who had been discharged or had died by Jan 31, 2020. Demographic, clinical, treatment, and laboratory data, including serial samples for viral RNA detection, were extracted from electronic medical records and compared between survivors and non-survivors. We used univariable and multivariable logistic regression methods to explore the risk factors associated with in-hospital death. Findings 191 patients (135 from Jinyintan Hospital and 56 from Wuhan Pulmonary Hospital) were included in this study, of whom 137 were discharged and 54 died in hospital. 91 (48%) patients had a comorbidity, with hypertension being the most common (58 [30%] patients), followed by diabetes (36 [19%] patients) and coronary heart disease (15 [8%] patients). Multivariable regression showed increasing odds of in-hospital death associated with older age (odds ratio 1·10, 95% CI 1·03–1·17, per year increase; p=0·0043), higher Sequential Organ Failure Assessment (SOFA) score (5·65, 2·61–12·23; p<0·0001), and d-dimer greater than 1 μg/mL (18·42, 2·64–128·55; p=0·0033) on admission. Median duration of viral shedding was 20·0 days (IQR 17·0–24·0) in survivors, but SARS-CoV-2 was detectable until death in non-survivors. The longest observed duration of viral shedding in survivors was 37 days. Interpretation The potential risk factors of older age, high SOFA score, and d-dimer greater than 1 μg/mL could help clinicians to identify patients with poor prognosis at an early stage. Prolonged viral shedding provides the rationale for a strategy of isolation of infected patients and optimal antiviral interventions in the future. Funding Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences; National Science Grant for Distinguished Young Scholars; National Key Research and Development Program of China; The Beijing Science and Technology Project; and Major Projects of National Science and Technology on New Drug Creation and Development.
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            SARS-CoV-2 Viral Load in Upper Respiratory Specimens of Infected Patients

            To the Editor: The 2019 novel coronavirus (SARS-CoV-2) epidemic, which was first reported in December 2019 in Wuhan, China, and has been declared a public health emergency of international concern by the World Health Organization, may progress to a pandemic associated with substantial morbidity and mortality. SARS-CoV-2 is genetically related to SARS-CoV, which caused a global epidemic with 8096 confirmed cases in more than 25 countries in 2002–2003. 1 The epidemic of SARS-CoV was successfully contained through public health interventions, including case detection and isolation. Transmission of SARS-CoV occurred mainly after days of illness 2 and was associated with modest viral loads in the respiratory tract early in the illness, with viral loads peaking approximately 10 days after symptom onset. 3 We monitored SARS-CoV-2 viral loads in upper respiratory specimens obtained from 18 patients (9 men and 9 women; median age, 59 years; range, 26 to 76) in Zhuhai, Guangdong, China, including 4 patients with secondary infections (1 of whom never had symptoms) within two family clusters (Table S1 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). The patient who never had symptoms was a close contact of a patient with a known case and was therefore monitored. A total of 72 nasal swabs (sampled from the mid-turbinate and nasopharynx) (Figure 1A) and 72 throat swabs (Figure 1B) were analyzed, with 1 to 9 sequential samples obtained from each patient. Polyester flock swabs were used for all the patients. From January 7 through January 26, 2020, a total of 14 patients who had recently returned from Wuhan and had fever (≥37.3°C) received a diagnosis of Covid-19 (the illness caused by SARS-CoV-2) by means of reverse-transcriptase–polymerase-chain-reaction assay with primers and probes targeting the N and Orf1b genes of SARS-CoV-2; the assay was developed by the Chinese Center for Disease Control and Prevention. Samples were tested at the Guangdong Provincial Center for Disease Control and Prevention. Thirteen of 14 patients with imported cases had evidence of pneumonia on computed tomography (CT). None of them had visited the Huanan Seafood Wholesale Market in Wuhan within 14 days before symptom onset. Patients E, I, and P required admission to intensive care units, whereas the others had mild-to-moderate illness. Secondary infections were detected in close contacts of Patients E, I, and P. Patient E worked in Wuhan and visited his wife (Patient L), mother (Patient D), and a friend (Patient Z) in Zhuhai on January 17. Symptoms developed in Patients L and D on January 20 and January 22, respectively, with viral RNA detected in their nasal and throat swabs soon after symptom onset. Patient Z reported no clinical symptoms, but his nasal swabs (cycle threshold [Ct] values, 22 to 28) and throat swabs (Ct values, 30 to 32) tested positive on days 7, 10, and 11 after contact. A CT scan of Patient Z that was obtained on February 6 was unremarkable. Patients I and P lived in Wuhan and visited their daughter (Patient H) in Zhuhai on January 11 when their symptoms first developed. Fever developed in Patient H on January 17, with viral RNA detected in nasal and throat swabs on day 1 after symptom onset. We analyzed the viral load in nasal and throat swabs obtained from the 17 symptomatic patients in relation to day of onset of any symptoms (Figure 1C). Higher viral loads (inversely related to Ct value) were detected soon after symptom onset, with higher viral loads detected in the nose than in the throat. Our analysis suggests that the viral nucleic acid shedding pattern of patients infected with SARS-CoV-2 resembles that of patients with influenza 4 and appears different from that seen in patients infected with SARS-CoV. 3 The viral load that was detected in the asymptomatic patient was similar to that in the symptomatic patients, which suggests the transmission potential of asymptomatic or minimally symptomatic patients. These findings are in concordance with reports that transmission may occur early in the course of infection 5 and suggest that case detection and isolation may require strategies different from those required for the control of SARS-CoV. How SARS-CoV-2 viral load correlates with culturable virus needs to be determined. Identification of patients with few or no symptoms and with modest levels of detectable viral RNA in the oropharynx for at least 5 days suggests that we need better data to determine transmission dynamics and inform our screening practices.
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              Correlation of Chest CT and RT-PCR Testing in Coronavirus Disease 2019 (COVID-19) in China: A Report of 1014 Cases

              Background Chest CT is used for diagnosis of 2019 novel coronavirus disease (COVID-19), as an important complement to the reverse-transcription polymerase chain reaction (RT-PCR) tests. Purpose To investigate the diagnostic value and consistency of chest CT as compared with comparison to RT-PCR assay in COVID-19. Methods From January 6 to February 6, 2020, 1014 patients in Wuhan, China who underwent both chest CT and RT-PCR tests were included. With RT-PCR as reference standard, the performance of chest CT in diagnosing COVID-19 was assessed. Besides, for patients with multiple RT-PCR assays, the dynamic conversion of RT-PCR results (negative to positive, positive to negative, respectively) was analyzed as compared with serial chest CT scans for those with time-interval of 4 days or more. Results Of 1014 patients, 59% (601/1014) had positive RT-PCR results, and 88% (888/1014) had positive chest CT scans. The sensitivity of chest CT in suggesting COVID-19 was 97% (95%CI, 95-98%, 580/601 patients) based on positive RT-PCR results. In patients with negative RT-PCR results, 75% (308/413) had positive chest CT findings; of 308, 48% were considered as highly likely cases, with 33% as probable cases. By analysis of serial RT-PCR assays and CT scans, the mean interval time between the initial negative to positive RT-PCR results was 5.1 ± 1.5 days; the initial positive to subsequent negative RT-PCR result was 6.9 ± 2.3 days). 60% to 93% of cases had initial positive CT consistent with COVID-19 prior (or parallel) to the initial positive RT-PCR results. 42% (24/57) cases showed improvement in follow-up chest CT scans before the RT-PCR results turning negative. Conclusion Chest CT has a high sensitivity for diagnosis of COVID-19. Chest CT may be considered as a primary tool for the current COVID-19 detection in epidemic areas. A translation of this abstract in Farsi is available in the supplement. - ترجمه چکیده این مقاله به فارسی، در ضمیمه موجود است.
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                Author and article information

                Contributors
                Role: Honorary Professor of Anaesthesia/Consultanttimcook007@gmail.com , @doctimcook
                Role: Professor/Consultant@wharropg
                Journal
                Anaesthesia
                Anaesthesia
                10.1111/(ISSN)1365-2044
                ANAE
                Anaesthesia
                John Wiley and Sons Inc. (Hoboken )
                0003-2409
                1365-2044
                01 June 2020
                : 10.1111/anae.15128
                Affiliations
                [ 1 ] Department of Anaesthesia and Intensive Care Medicine Royal United Hospitals Bath NHS Foundation Trust Bath UK
                [ 2 ] University of Bristol UK
                [ 3 ] Department of Anaesthesia Imperial College Healthcare NHS Trust London UK
                [ 4 ] Imperial College London UK
                Author notes
                [*] [* ] Correspondence to: T. M. Cook

                Email: timcook007@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-3654-497X
                Article
                ANAE15128
                10.1111/anae.15128
                7276860
                32428245
                f19afafa-b1fe-4c58-a5c0-65c5d34a1d51
                © 2020 Association of Anaesthetists

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 15 May 2020
                Page count
                Figures: 0, Tables: 0, Pages: 5, Words: 9717
                Categories
                Editorial
                Editorial
                Custom metadata
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                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.4 mode:remove_FC converted:08.06.2020

                Anesthesiology & Pain management
                covid‐19,peri‐operative,surgery
                Anesthesiology & Pain management
                covid‐19, peri‐operative, surgery

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