Polyneuropathies
Conditions
Keywords
Critical illness, Critical illness polyneuropathy and/or myopathy, Intravenous immunoglobulins, Multiple organ failure, SIRS, Sepsis
Brief summary
Critical illness polyneuropathy and/or myopathy (CIPNM) is a severe complication of critical illness. Retrospective data suggest that early application of IgM-enriched intravenous immunoglobulin (IVIG) may prevent or mitigate CIPNM. Therefore, the primary objective was to assess the effect of early IgM-enriched IVIG versus placebo to mitigate CIPNM in a prospective setting.
Detailed description
Background: Critical illness polyneuropathy and/or myopathy (CIPNM) is a severe complication of critical illness. Retrospective data suggest that early application of IgM-enriched intravenous immunoglobulin (IVIG) may prevent or mitigate CIPNM. Therefore, the primary objective will be to assess the effect of early IgM-enriched IVIG versus placebo to mitigate CIPNM in a prospective setting. Design: Prospective, randomized, double-blinded and placebo-controlled trial Setting: Eight-bed medical ICU of a university hospital. Participants: Critically ill patients will be screened for eligibility defined as multiple organ failure (MOF) and SIRS/sepsis. Patients fulfilling these criteria will be further assessed by a neurologist for clinical signs of CIPNM. Critically ill patients with multiple organ failure (MOF), SIRS/sepsis, and early clinical signs of CIPNM will be randomized.
Interventions
DRUGIgM-enriched Intravenous Immunoglobulins
IgM-enriched IVIG (Pentaglobin, Biotest Pharma GmbH, Dreieich, Germany) at a dose of 0.25g/kg body weight/day as a continuous intravenous infusion at a rate of 2g/h over a period of 3 days.
DRUGHuman Albumin
Human albumin 1% (Biotest Pharma GmbH, Dreieich, Germany) as placebo at a dose of 0.25g/kg body weight/day as a continuous intravenous infusion at a rate of 2g/h over a period of 3 days
Sponsors
Biotest Pharma GmbH
National Bank of Austria
Medical University of Vienna
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Critically ill patients with failure of at least 2 organ systems diagnosed with SIRS or sepsis fulfilling the following inclusion criteria will be included in this study. 1. Age Range: 18 - 80 years 2. written information and consent as early as possible 3. Male and female patients 4. Clinical signs of incipient CIPNM: * decreased tendon reflexes as compared to the admission examination at the ICU * or weakness in responsive and co-operative patients as compared to the ad-mission examination at the ICU * or signs of incipient muscular atrophy as compared to the admission examination at the ICU Organ failure: Patients have to meet at least two of the following 5 criteria: * cardiovascular system dysfunction: arterial systolic blood pressure\<90mm Hg, or mean arterial pressure \< 70mm Hg for at least one hour despite adequate fluid resuscitation, adequate intravascular volume status or the use of vasopressors in an attempt to maintain a systolic blood pressure \>90mm Hg or a mean arterial pressure \>70mm Hg. * kidney dysfunction: Urine output \< 0,5ml/kg body weight/ hour for 1 hour, despite adequate fluid resuscitation * respiratory system dysfunction: Ratio of PaO2 to FiO2 \< 250 in the presence of other dysfunctional organs or systems * hematologic dysfunction: Platelet count \<80.000/mm3 or decreased by 50% in the 3 days preceding enrollment (in the absence of liver cirrhosis or previously known hematological disease) * metabolic dysfunction: In case of unexplained metabolic acidosis - pH\<7,30 or base deficit \>5.0mmol/ litre in association with a plasma lactate level \>1,5 times of the upper normal limit SIRS: Patients have to meet at least three of the following four criteria: * core temperature \>38 or \<36°C * heart rate \>90 beats /min, except medical conditions known to increase heart rate * respiratory rate \>20 breaths/min or a PaCO2 of \<32mm Hg or the use of mechanical ventilation for an acute respiratory process * a white- cell count of\>12.000 cells/mm3 or \<4.000 cells/mm3 or a differential count showing \>10% immature neutrophils Sepsis: Known or suspected infection evidenced by one or more of the following: * white cells or bacteria in a normally sterile body fluid * perforated viscus * radiographic evidence of pneumonia in the association with the production of purulent sputum * a syndrome associated with a high risk of infection
Exclusion criteria
The inclusion criteria have to be met at the time of enrolment into the study, i.e. at the start of the baseline period. Patients with any of the following conditions will be excluded from the study: 1. Age \< 18 years or \> 80 years 2. Weight \>135 kg 3. Pregnancy or breast-feeding 4. Patients with known absolute IgA-deficiency with proven antibody formation against IgA 5. Patients with known IVIG-intolerability 6. Patients with known pre-existing neuromuscular disorders will not be included. Patients with documented pre-existing severe polyneuropathy will be excluded. 7. Patients with known diseases of the peripheral nerval system and patients with pre-existing disease of the central nerval system with relevant impairment of the motor function. 8. Patients with relevant pulmonary edema secondary to severe heart failure will be excluded because of the relatively high infusion volume (5ml /kg body weight per day over 3 days) determined by the study medication 9. Patients not expected to survive 28 days because of uncorrectable medical condition, such as poorly controlled neoplasma or other end-stage disease 10. Moribund state in which death is perceived to be imminent 11. HIV infection in association with a last known CD4 count of\<50/mm3 12. Prediction, based on clinical judgement, that the patient will require chronic ventilatory support for non-respiratory reasons (e.g. neuromuscular disease, paraplegia
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Effect of early IVIG versus placebo on CIPNM on day 14 | day 14 | The primary outcome was to assess the effect of early IVIG (IgM-enriched Intravenous immunoglobulins) versus placebo to mitigate CIPNM in critically ill patients as assessed by the CIPNM severity sum score on day 14. The CIPNM severity sum score is based on electrophysiological stimulation of the median, ulnar, and tibial nerves on days 0, 4, 7, 14 and on the histological evaluation of muscle biopsies on days 0 and 14 and ranged from 0 (no CIPNM) to 8 (very severe CIPNM). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Effect of early IVIG versus placebo on mortality from any cause within a 28-day period | 28 days | This secondary outcome aimed to assess the effect of early IVIG versus placebo on mortality from any cause within a 28-day period. |
| Effect of early IVIG versus placebo on length of the ICU stay. | ICU stay, an expected average of 30 days | This secondary outcome aimed to assess the effect of early IVIG versus placebo on the length of the ICU stay. Length of ICU stay is defined as the time difference difference between admission of the patient to the ICU and discharge to a (non-ICU) ward or death. This outcome will be assessed an the day of ICU discharge. |
Countries
Austria
Outcome results
None listed