Middle East respiratory syndrome coronavirus infection medical therapy: Difference between revisions

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====Section 1====
====Section 1====
This section aims for the early recognition and management of symptoms. This includes:
This section aims for the early recognition and management of symptoms. This includes:
*Recognition of severe manifestations of acute respiratory infections
*Initiation of infection prevention and control measures
*Providing supplemental oxygen therapy to patients with severe acute respiratory infections
*Collection of respiratory and other specimens for laboratory testing
*Administration of empiric antimicrobials to treat suspected pathogens, including community-acquired pathogens
*Administration of conservative fluid management in patients with severe acute respiratory infections when there is no evidence of shock
*Close monitoring of patients with severe acute respiratory infections for signs of clinical deterioration, such as severe respiratory distress/respiratory failure or tissue hypoperfusion/shock, and apply supportive care interventions
*Avoid high-dose systemic corticosteroids or other adjunctive therapies for viral pneumonitis outside the context of clinical trials


====Section 2====
====Section 2====

Revision as of 03:29, 18 June 2014

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

Middle East Respiratory Syndrome (MERS) is a viral respiratory illness. It is caused by an emerging coronavirus, specifically a betacoronavirus called MERS-CoV (Middle East Respiratory Syndrome Coronavirus), first discovered in 2012. Being a relatively novel virus, there is no virus-specific prevention or treatment options for MERS patients. Outbreaks of MERS-CoV represent a great social challenge due to the fact that there is very limited time to develop and test new pharmaceutical drugs. The common clinical presentations documented so far include Acute Respiratory Distress Syndrome (ARDS), renal failure, pericarditis and disseminated intravascular coagulation. Therefore the supportive care should focus mainly in the prevention and monitoring of these conditions. Until now, supportive medical care has been the only treatment option, however, repurpose of drugs for other viruses and illnesses is presenting as an attractive alternative for MERS-CoV.[1][2]

Medical Therapy

MERS represents a great challenge in terms of treatment because it is caused by a relatively novel virus to which there is no approved therapy yet. According to the International Severe Acute Respiratory & Emerging Infection Consortium (ISARIC), supportive medical care continues to be the approved treatment for MERS. The search for broad-spectrum inhibitors aiming to minimize the impact of coronavirus infection remains the major goal. Recent studies are showing the potential use of other drugs and therapies to treat the MERS-CoV, which are based on the experience of treatment of other coronaviruses like the SARS virus. This repurposing of drugs has advantages such as: better availability, lower cost and known safety and tolerability profiles. However, lack of evidence makes these new therapies uncertain.[1]

Cell and animal studies have shown conflicting results: the combination of ribavirin with interferon α-2b in a cell study reduced viral replication[3]; another study in rhesus monkeys with combination of intramuscular ribavirin and interferon α-2b, the group that received the treatment did not develop breathing abnormalities nor radiographic evidence of pneumonia[4]; however, when tried in 5 critically ill patients in Saudi Arabia, this combination was inefficient in all cases, leading to a fatal outcome.[5]

Despite the absence of a specific therapy, some approaches are considered to be more worth of experimentation than others. These include:[6][7][8][2][9]

Supportive Care

The supportive medical care aims to minimize as much as possible the damages caused by MERS. It is divided into 4 categories, according to the clinical management steps required for the current health status of the MERS patient. These categories include:[2]

  • Section 1 - focuses on the early recognition and management of patients with severe acute respiratory infections and includes early initiation of supportive and infection prevention, control measures and therapeutics
  • Section 2 - focuses on management of patients who deteriorate and develop severe respiratory distress and ARDS
  • Section 3 - focuses on the management of patients who deteriorate and develop septic shock
  • Section 4 - focuses on ongoing care of the critically ill patient and best practices to prevent complications

Section 1

This section aims for the early recognition and management of symptoms. This includes:

  • Recognition of severe manifestations of acute respiratory infections
  • Initiation of infection prevention and control measures
  • Providing supplemental oxygen therapy to patients with severe acute respiratory infections
  • Collection of respiratory and other specimens for laboratory testing
  • Administration of empiric antimicrobials to treat suspected pathogens, including community-acquired pathogens
  • Administration of conservative fluid management in patients with severe acute respiratory infections when there is no evidence of shock
  • Close monitoring of patients with severe acute respiratory infections for signs of clinical deterioration, such as severe respiratory distress/respiratory failure or tissue hypoperfusion/shock, and apply supportive care interventions
  • Avoid high-dose systemic corticosteroids or other adjunctive therapies for viral pneumonitis outside the context of clinical trials

Section 2

Section 3

Section 4

References

  1. 1.0 1.1 Dyall J, Coleman CM, Hart BJ, Venkataraman T, Holbrook MR, Kindrachuk J; et al. (2014). "Repurposing of clinically developed drugs for treatment of Middle East Respiratory Coronavirus Infection". Antimicrob Agents Chemother. doi:10.1128/AAC.03036-14. PMID 24841273.
  2. 2.0 2.1 2.2 "Clinical management of severe acute respiratory infections when novel coronavirus is suspected: What to do and what not to do" (PDF).
  3. Falzarano D, de Wit E, Martellaro C, Callison J, Munster VJ, Feldmann H (2013). "Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin". Sci Rep. 3: 1686. doi:10.1038/srep01686. PMC 3629412. PMID 23594967.
  4. Falzarano D, de Wit E, Rasmussen AL, Feldmann F, Okumura A, Scott DP; et al. (2013). "Treatment with interferon-α2b and ribavirin improves outcome in MERS-CoV-infected rhesus macaques". Nat Med. 19 (10): 1313–7. doi:10.1038/nm.3362. PMID 24013700.
  5. Al-Tawfiq JA, Momattin H, Dib J, Memish ZA (2014). "Ribavirin and interferon therapy in patients infected with the Middle East respiratory syndrome coronavirus: an observational study". Int J Infect Dis. 20: 42–6. doi:10.1016/j.ijid.2013.12.003. PMID 24406736.
  6. "Treatment of MERS-CoV: Decision Support Tool".
  7. Guery B, van der Werf S (2013). "Coronavirus: need for a therapeutic approach". Lancet Infect Dis. 13 (9): 726–7. doi:10.1016/S1473-3099(13)70153-1. PMID 23782860.
  8. Ren Z, Yan L, Zhang N, Guo Y, Yang C, Lou Z; et al. (2013). "The newly emerged SARS-like coronavirus HCoV-EMC also has an "Achilles' heel": current effective inhibitor targeting a 3C-like protease". Protein Cell. 4 (4): 248–50. doi:10.1007/s13238-013-2841-3. PMID 23549610.
  9. Momattin H, Mohammed K, Zumla A, Memish ZA, Al-Tawfiq JA (2013). "Therapeutic options for Middle East respiratory syndrome coronavirus (MERS-CoV)--possible lessons from a systematic review of SARS-CoV therapy". Int J Infect Dis. 17 (10): e792–8. doi:10.1016/j.ijid.2013.07.002. PMID 23993766.

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