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Therapeutic Plasma Exchange in Resistant Cytokine Storm of COVID 19

Does Therapeutic Plasma Exchange Have A Role in Resistant Cytokine Storm State Of COVID-19 Infection?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04457349
Enrollment
10
Registered
2020-07-07
Start date
2020-07-25
Completion date
2021-01-20
Last updated
2022-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID 19

Brief summary

This research is planned to illustrate the efficacy of Therapeutic Plasma Exchange (TPE) treatment in COVID-19 patients with resistant cytokine storm state.

Detailed description

In early December 2019, several pneumonia cases of unknown origin were observed in Wuhan (China). A novel enveloped RNA β coronavirus was isolated and named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The new virus rapidly spread across China and worldwide. On March 11th 2020, the World Health Organization (WHO) declared coronavirus disease 2019 (COVID-19) a pandemic. As of 19June 2020, COVID-19 has been confirmed in 8,385,440 individuals globally with deaths reaching 450,686 with a morality of 5.37%. Egypt has 50,437 confirmed cases and 1938 deaths. The virus mainly spreads through respiratory droplets from infected patients.The clinical spectrum of COVID-19 infection ranges from asymptomatic forms to severe pneumonia requiring hospitalization and isolation in critical care units with the need of mechanical ventilation due to acute respiratory distress syndrome (ARDS). Main symptoms include fever, fatigue and dry cough. Common laboratory findings include lymphopenia and elevated lactate dehydrogenase levels. Platelet count is usually normal or mildly decreased. C reactive protein (CRP) and erythrocyte sedimentation rate are usually increased while procalcitonin levels are normal and elevation of procalcitonin usually indicates secondary bacterial infection. Ferritin, D-dimer, and creatine kinase elevation is associated with severe disease. Chest computed tomographic scans show a typical pattern of bilateral patchy shadows or ground glass opacity. Severe COVID-19 conditions are usually due to an aggressive inflammatory response known as cytokine storm that is characterized by the release of a large amount of pro-inflammatory cytokines. Lung injury, multiorgan failure, and unfavorable prognosis of severe COVID-19 infection have been attributed mainly to the cytokine storm state. Many proinflammatory cytokines elevate in COVID-19 patients including IL-1, IL-6, IL-8, IL-10, tumour necrosis factor α (TNF-α) and interferon Ȣ(IFN-Ȣ) stimulating immune cells to invade sites of infection causing endothelial dysfunction, vascular damage, alveolar damage and ARDS. Cytokine storm has been reported in several viral infections including influenza H5N1 virus, influenza H1N1 virus, and the two coronaviruses highly related to COVID-19; SARS-CoV and MERS-CoV. Therapeutic approaches to manage the COVID-19 cytokine storm might provide an avenue to decrease the COVID-19 associated morbidity and mortality. Options include immunomodulators, cytokine antagonists and cytokine removal. Tocilizumab (IL-6 antagonist), Anakinra (antagonist of IL-1 β), TNF blockers, ruxolitinib (JAK1/2 inhibitor ), corticosteroids, intravenous immunoglobulins and therapeutic plasma exchange (TPE) have been used with variable efficacy. Therapeutic plasma exchange can remove inflammatory factors, block the cytokine storm, to reduce the damage of inflammatory response to the body. This therapy can be used for severe and critical patients in the early and middle stages of the disease. Patel and colleagues utilized TPE during the 2009 H1N1 influenza A outbreak in three pediatric patients presenting in a similar fashion to those seen with fulminant COVID-19 today. All three had full recovery from their illness after receiving rescue TPE. Adeli at al. used TPE as a rescue therapy in patients with severe forms of COVID-19 ( septic shock, ARDS ) with very good results. Out of 8 patients, 7 patients improved and one patient died. Zhang et al. also tried TPE in three COVID-19 patients who despite receiving antiviral treatment developed respiratory distress and levels of IL-6 increased rapidly. All patients improved clinically and radiologically with negative nucleic acid testing and were discharged 10-14 days later. In Egypt, the first line drug to treat cytokine storm of COVID-19 is tocilizumab with good results. But a considerable percentage of patients do not respond to it leaving physicians with very limited options and usually patients deteriorated rapidly with high mortality. Based on the encouraging results of TPE in severe COVID-19 infections and the familiarity of the procedure, TPE could be a good option in those patients who do not respond to tocilizumab.

Interventions

Treatment with Therapeutic Plasma Exchange (TPE)

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* COVID-19 positive patients (confirmed by PCR) with cytokine storm state who will not improve after two doses of tocilizumab. * Criteria of failure (resistance) to tocilizumab: 1. Persistent high IL-6 and CRP. 2. Persistent worsening of respiratory symptoms ( dyspnea, tachypnea, increased oxygen (O2) requirements or even need for mechanical ventilation). 3. Partial arterial pressure of oxygen to fractional inspired concentration of oxygen (PaO2/FiO2) ratio \< 150. 4. Persistent fever (˃38.5°C) despite normal procalcitonin level.

Exclusion criteria

* Refractory septic shock: ( It is defined according to surviving sepsis campaign as the presence of hypotension with end organ dysfunction requiring high dose vasopressor support often greater than 0.5 µg/kg/min norepinephrine or equivalent).

Design outcomes

Primary

MeasureTime frameDescription
mortality28 dayNumber of patients deaths of the total of patients included

Secondary

MeasureTime frameDescription
the mean time with Non-invasive mechanical ventilationthrough study completion, and average of 1 monthto calculate the mean time with Non-invasive mechanical ventilation
the mean time of intubationthrough study completion, and average of 1 monthto calculate the mean time of intubation
respiratory function parametersthrough study completion, and average of 1 monthTo calculate the mean of PaO2/FiO2
radiological lung extensionthrough study completion, and average of 1 monthto evaluate the lung extension of pneumonia
mean duration of hospitalization and ICU usethrough study completion, and average of 1 monthDays of hospitalization in survivors and/or days at ICU throughout the study
the requirement of additional organ supportthrough study completion, and average of 1 monthPercentage of patients with dialysis
the mean time with oxygen therapythrough study completion, and average of 1 monthto calculate the mean time with oxygen therapy
Incidence of adverse eventsthrough study completion, and average of 1 monthTo calculate the number of adverse events in patients with COVID-19 treated with TPE
time to reverse-transcriptase polymerase chain reaction (RT-PCR) virus negativitythrough study completion, and average of 1 monthTo evaluate the time to RT-PCR virus negativity
the levels of CRPthrough study completion, and average of 1 monthTo evaluate the effect of TPE on the serum levels of inflammatory markers
the levels of procalcitonin (PCT)through study completion, and average of 1 monthTo evaluate the effect of TPE on the serum levels of inflammatory markers
levels of D-dimerthrough study completion, and average of 1 monthTo evaluate the effect of TPE on the serum levels of inflammatory markers
levels of ferritinthrough study completion, and average of 1 monthTo evaluate the effect of TPE on the serum levels of inflammatory markers
the levels of IL-6through study completion, and average of 1 monthTo evaluate the effect of TPE on the serum levels of inflammatory markers

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026