Early Oseltamivir Carboxylate Low Plasma Concentration in Patients Admitted to Intensive Care for Severe Influenza

Severe Influenza Clinical Trial

— OPTIFLU  

Official title:

Prognostic Impact of Early Oseltamivir Carboxylate Low Plasma Concentration in Critically Ill Patients With Severe Influenza: a Prospective Cohort Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05375864
• Other study ID #: APHP210090
• Secondary ID: 2022-002377-28
• Status: Not yet recruiting
• Phase: N/A
• Start date: December 1, 2022
• Est. completion date: March 1, 2025

Study information

• Verified date: November 2022
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Anne-Fleur Haudebourg, M.D
• Phone: 01 45 17 85 06
• Email: annefleur.maignant[@]aphp.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Introduction

Pandemic and seasonal influenza epidemics can be associated with a high degree of morbidity and mortality, especially in patients developing severe influenza pneumonitis with the acute respiratory distress syndrome (ARDS) or the less frequent fulminant myocarditis. Early administration (i.e. in the first 48 hours) of the neuraminidase inhibitor oseltamivir is associated with reduced mortality in patients hospitalized for severe influenza. Early oseltamivir administration, which can only be given orally (or through a nasogastric tube), is thus recommended by the World Health Organization in patients hospitalized for severe influenza, including those requiring intensive care (ICU) admission. However, enteric absorption may be compromised in critically ill patients due to impaired gut function.

Hypothesis/Objective

The hypothese is that, in patients admitted for severe influenza, early (i.e., measured at the 48th hour of treatment initiation) oseltamivir carboxylate (OC) low plasma concentration would be: 1) associated with a poor prognosis; and 2) detectable by carrying out a paracetamol absorption test (PAT).

The main objective of the study is to determine the prognostic impact of early OC low plasma concentration in patients admitted to the intensive care unit (ICU) for severe influenza.

Primary outcome measure: Number of live ventilator-free days at 28-day in patients with versus without OC low plasma concentration.

Description:

Methods

Prospective cohort study conducted in 22 French intensive care units. Adult patients admitted to the ICU for severe influenza requiring invasive mechanical ventilation and treated with oseltamivir through a gastric tube for less than 24 hours will be included.

After inclusion, oseltamivir treatment will be continued through a gastric tube (75mg x 2 /day). After the 4th administration, plasma peak concentration of oseltamivir phosphate (OP) will be dosed at 60 minutes (CmaxOP) and plasma residual concentration of OC will be dosed at 12 hours (just before the 5th dose) (CresOC). A paracetamol absorption test will also be performed at the same time (consisting in the measurement of plasma paracetamol concentration 60 minutes after enteral loading with 1000 mg of paracetamol). CmaxOP and CresOC will also be measured at day 3 and 5 in order to realize pharmacokinetic analysis. Nasal swabs will be performed at inclusion (day 1) and day 5 for viral load quantification and viral strain sequencing (detection of the H275Y mutation). Clinical and biological variables will be collected from day 1 to day 90.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 155
• Est. completion date: March 1, 2025
• Est. primary completion date: December 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients

• Confirmed severe influenza infection requiring intensive care with tracheal intubation for invasive mechanical ventilation (influenza ARDS with or without bacterial co-infection, cardiorespiratory decompensation of influenza origin, influenza myocarditis)

• Oseltamivir treatment administered through a gastric tube initiated since less than 24 hours (i.e. maximum two doses administered)

• Affiliation to a social security system or beneficiary (excluding AME)

• Written consent obtained (or under emergency procedures)

Exclusion Criteria:

• Pregnancy or breastfeeding women

• Weight less than 40 kg

• Zanamivir or other antiviral effective treatment received for more than 24 hours

• Other respiratory virus infection (including SARS-CoV-2)

• Contra-indication to esophageal tube insertion or use

• Child-Pugh C cirrhosis or severe liver insufficiency

• Paracetamol allergy

• Ongoing participation in an interventional therapeutic trial (medicine that may interact with paracetamol or oseltamivir)

• Patient benefiting from AME (State Medical Aid)

• Patient deprived of liberty or under legal protection (guardianship or curatorship)

• For patients not included in an emergency situation: Inability, according to the investigator, to understand or refusal to sign the informed consent to participate in the study (non-French-speaking patient).

Related Conditions & MeSH terms

• Influenza, Human
• Severe Influenza

Intervention

Other:
• Absorption test
Paracetamol's administration (1 gram) - 48 hours after oseltamivir administration.

Locations

Country	Name	City	State
France	Anne-Fleur Haudebourg	Créteil

Sponsors (1)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Live ventilator-free days (VFDs)	VFDs = 0 if subject dies within 28 days of mechanical ventilation. VFDs = 28 - x if successfully liberated from ventilation x days after initiation.; VFDs = 0 if the subject is mechanically ventilated for > 28 days.	Day 28
Secondary	Diagnostic performance of the paracetamol absorption test (PAT)	Sensitivity = ability of PAT to correctly classify a patient as "having a low oseltamivir carboxylate (OC) concentration" = (true positive) / (true positive + false negative) Specificity = ability of PAT to correctly classify a patient as "not having a low oseltamivir carboxylate (OC) concentration" = (true negative) / (true negative + false positive) Positive predictive value (PPV) = percentage of patients with negative PAT who actually are "having a low oseltamivir carboxylate (OC) concentration"= (true positive) / (true positive + false positive) Negative predictive value (NPV) = percentage of patients with positive PAT who actually are not ""having a low oseltamivir carboxylate (OC) concentration" = (true negative) / (false negative + true negative) Positive Likelihood Ratio = Sensitivity / (1 - Specificity) Negative Likelihood Ratio = (1 - Sensitivity) / Specificity	48 hours
Secondary	Prevalence of patients with low plasma OC concentration		48 hours
Secondary	Independent variables present on admission associated with low plasma OC concentration		48 hours
Secondary	Prevalence of acquisition early OC concentration and viral clearance		48 hours
Secondary	Prevalence of acquisition of the oseltamivir resistance mutation (H275Y) in patients with versus without low plasma OC concentration.		48 hours and day 5
Secondary	Maximum oseltamivir carboxylate concentrations measurement		Days 2, 3 and 5
Secondary	Maximum oseltamivir phosphate concentrations measurement		Days 2, 3 and 5
Secondary	Residual oseltamivir carboxylate concentrations measurement		Days 2, 3 and 5
Secondary	Residual oseltamivir phosphate concentrations measurement		Days 2, 3 and 5
Secondary	Mortality		Days 28 and 90