key: cord-0692336-mfiaubqb authors: Gupta, Naveen; Singhai, Monil; Garg, Shubha; Shah, Dhara B.; Sood, Vishesh; Singh, Sujeet kr title: The missing pieces in the jigsaw and need for cohesive research amidst COVID 19 global response date: 2020-04-07 journal: Med J Armed Forces India DOI: 10.1016/j.mjafi.2020.04.001 sha: d2bcf551df384f34222ec31b16167163aac2b34d doc_id: 692336 cord_uid: mfiaubqb nan Type of article: Guest editorial / Op-ED / Perspective Name(s) of the author(s) with the highest academic degree (Kindly provide for each author. All the fields given in the table below are mandatory. Please add more rows if you need to include more authors. Please list the authors in the order of contribution and indicate corresponding author using an asterisk (*) at the end of the name. The corresponding author must be the one making the submission). 4 The pandemic has clearly entered a new stage with rapid spread in many countries outside China. Various containment and mitigation strategies focus at delaying major surges of patient-load and levelling the demand for hospital beds while also protecting the most vulnerable groups such as elderly people and those with co-morbidities. To make every strategy work, a clear understanding of what we know and what we don't know is critically important to frame genuine strategies by subject experts. Hence, identifying the research needs and gaps amidst this pandemic is absolutely important for improving the way we think and the way we act. It is important to know the natural history of the disease as well as viral shedding in different stages of clinical illness. Viral shedding can vary from acute to convalescent to post-recovery phase as well. Host factors such as young children and immunocompromised population may also matter. Host infection following transmission of the virus is dependent on local mucosal immunity to natural immunity or crossprotection or vaccine induced immunity. Virus stability in community or hospital environment may vary and determines a high or low risk of transmission depending upon the significant exposure of the host. Animal models may also help in studying the pathogenesis of COVID-19. With COVID-19, we need to identify all possible animal sources and routes of transmission as they determine the persistence in animals ranging from infection to disease to being a reservoir. Accidental or continuous spill-over to human beings usually determines the length of exposure and consequent outbreaks. 5 Socio-economic and behavioural risk factors in various societies and geographic regions also play a critical role. Various risk reduction strategies at human, animal and environmental interface need to be studied for defining the high-risk situations. We need to understand the spread of the disease nationally, regionally, and globally with clearly defined surveillance case definitions for cases and contacts of COVID-19. Defining the susceptible population at risk and high-risk groups will be extremely useful to develop the containment strategy. Hypotheses developed for transmission dynamics in community or hospital and defining the laboratory criteria for the case confirmation will be most crucial in terms of clear understanding and interventions needed for containment of an outbreak. Non-pharmaceutical interventions on transmissibility can reduce the number of total cases. Social distancing can be one of the most effective measures to reduce the peak burden on the health care system. 6 Overall, the impact of the outbreak as well as the interventions also needs timely and frequent assessment. Surveillance of influenza-like illness (ILI) and severe acute respiratory infections (SARI) can contribute to the detection of COVID-19 cases. 7 Always an attempt should be made to collect the direct evidence of the disease by isolation or detection of RNA by PCR. SARS-CoV-2 isolation is not recommended for diagnostic laboratories; however, it is useful for developing the diagnostic kits and candidate vaccines. Various types of protocols targeting various genes may require comparison only from research point of view; however, screening and confirmatory targets defined by regional reference laboratories may be followed by most for the purpose of traceability and reproducibility. Mechanisms to check the indeterminate results must lie with national reference laboratory. Gene sequencing must be submitted by all molecular biologists to GenBank to study the strain variations or mutations and molecular evolution. Serological tests for COVID-19 need to be validated with the relevant standards and maybe used for surveillance only. Validation and suitable use of molecular based test such as qRT-PCR should be clearly evaluated for diagnosis and/or surveillance. In context of an outbreak or pandemic, it is extremely important for the health care delivery system to be adequately prepared with appropriate personal protective equipment (PPE) and know the clinical course of the disease along with the common and uncommon presentations. The understanding of natural history/course of COVID-19 will help in triaging the patients in hospital settings. Defining the clinical case definitions and sampling strategy will help in differentiating COVID-19 from other similar illnesses with or without pneumonia. Ignoring other differential diagnosis can invariably be counterproductive from diagnosis and management point-of-view. Studying prognosis factors in COVID-19 confirmed cases will help in developing comprehensive management plan/approach with combination of various drugs or instituting newer therapeutics of proven or experimental efficacy. Transmission of COVID-19 in health care workers (HCW) is a cause of deep concern, hence, all three precautions -droplet, contact and airborne must be suitably practiced by every health care personnel. Keeping daily records of medical examination of HCW can help in early detection and further spread. Continuous training appropriate at each level must also be documented. Hospital admission and discharge policies need to be defined in consonance with national policy. Logistics for PPE and other consumables needs to be ensured. Only trained personnel in batches may be allowed to work. The expert advice must be readily available in case of breech of unprecedented practice. Optimization and re-use of certain consumables/ supplies may be permitted as per safety norms. The scope of newer diagnostics and treatment approaches will pave the way for defining the future guidelines. Collaborations with other departments and institutes will produce results of higher notch. For COVID-19, Infection Control committee should supervise on daily basis and identify the gaps and provide necessary resources and directions to minimize the transmission. Starting from entry in hospital premises, the movement control strategy must be defined to prevent secondary transmission in healthcare as well as in community settings. Optimum and effective use of PPE in designated areas will play a crucial role in reducing the risk of transmission in health care workers. 8 Behavioural and cultural factors must also be taken into an account as they influence the compliance. Quarantine facilities should be welldesigned and away from habitation. Isolation facilities with separate rooms and negative air pressure in case of suspected and confirmed COVID-19 positive cases will substantially be useful for containment as well as protection of health workers. Personnel may be trained for DOs and DON'Ts in quarantine facility. Identification of candidate therapeutics for SARS CoV2 needs an overall strategy encompassing research, development, and regulatory compliance. Repurposing of drug molecules is an elegant strategy to develop therapeutics in the case of pandemics quickly. The general plan for repurposing can involve computational approaches to determine the likelihood of a drug molecule to affect SARS CoV2 based on its similarity to the known target of that molecule. 9 Another method is to experimentally study the interaction between proteins of SARS CoV2 and humans and use it to develop a list of therapeutic candidates. Prophylaxis will play an essential role in the elimination of COVID-19 in the long run. However, a successful vaccine will require the development and standardization of animal models to check for the efficacy of vaccine candidates using a challenge study. Only after successful animal studies, vaccine candidates can be taken to clinical trials. The clinical trial phase requires standardized assays to evaluate immune response in humans. The other aspect which needs a more concerted effort is to have regulatory compliance for developed targets for therapeutics and vaccine. In the case of a pandemic, the usual route of clinical trials is too cumbersome and may take years to develop a therapeutic intervention. The use of adaptive clinical trial designs will help in expediting regulatory approval. 10 Adaptive clinical trials such as multi-arm multi-stage (MAMS) trials aim at using the real-world clinical practice of learning and reacting as and when an event happens. The flexibility of MAMS allows changing the course of a clinical trial without compromising its integrity or validity, thereby ensuring that more patients receive better treatments. Regulatory authorities and research bodies may allow such school of thoughts to expedite the development of therapeutics and vaccines. In view of lack of established protocols and critical knowledge gaps, basic ethical standards must address the management issues regarding COVID-19 and maybe formed at the level of organization or as national policy. The national needs in terms of geography, population, social and cultural practices are different and hence, ethical considerations may be based upon reality and practices. Unproven practices and treatment protocols should invite critical scrutiny on the basis of ethics. We need knowledge, attitude and practice studies in terms of acceptance and adherence to public health measures and other health initiatives for COVID-19. Accessing and addressing the physical health and psychosocial well-being of health care workers involved in care giving for COVID-19 from time-to-time. Risk assessment and communication to address the public health needs and measures will help the general public to address their issues of anxiety, fear, and stigma associated with the COVID-19. There is also a need to understand the effect of restrictive public health measures used for management of COVID-19 (such as quarantine, isolation, lockdowns, etc.) on the psychosocial and physical wellbeing of individuals. Socioeconomic status of the communities is also an important determinant for the compliance of sustainable public health measures. Public health information system must address pertinent issues based on dynamics of COVID-19 and effectiveness of the control measures. First and foremost, a political commitment and funding from topmost level is essential. It is also essential to optimise the standard of patient care at different stages of the disease and take advantages of all available technological innovations to improve the prognosis. Early evaluation of the effect of adjunctive and supportive therapies will be substantially useful. There should be a rational use of PPE and other infection prevention and control measures in health care and community settings. We should review the available scientific information to identify animal host(s) for preventing continued spill-over and better understanding of various aspects related to SARS CoV2 transmission such as time duration, severity of disease and host susceptibility. The evaluation of investigational therapeutics and vaccines needs to be expedited. We need to mobilize research on rapid point of care diagnostics at community level. It is very important that there is efficient data sharing for immediate public health purposes and conducting research activities. Comprehensive strategy with a holistic approach in preparedness may allow the rapid activation of research and development activities during pandemic. Its aim should be fasttracking availability of effective diagnostics, vaccines and therapeutics that can avert the crisis and lead to effective management of COVID-19 pandemic. Scientists working on Research and Development at various regional/national levels may also be aligned to global efforts for containment/control of COVID-19. Naming the coronavirus disease (COVID-19) and the virus that causes it World Health Organization. Statement on the second meeting of the International Health Regulations (2005) Emergency Committee regarding the outbreak of novel coronavirus statement-on-the-second-meeting-of-the-international-health-regulations-(2005)-emergency-committee-regarding-the-outbreak World Health Organization. WHO Director-General's opening remarks at the media briefing on COVID-19 -11 Pathways to zoonotic spillover The effect of control strategies to reduce social mixing on outcomes of the COVID-19 epidemic in Wuhan World Health Organization. Laboratory testing strategy recommendations for COVID-19 World Health Organization. Rational use of personal protective equipment (PPE) for coronavirus disease Network-based drug repurposing for novel coronavirus 2019-nCoV/SARS-CoV-2 Adaptive trial designs: what are multiarm, multistage trials? Archives of disease in childhood -Education &