Discontinuation of imipenem-cilastatin or meropenem
DrugDiscontinuation of imipenem-cilastatin or meropenem after 3x24 hours irrespective of presence of fever.
Other names: tienam (imipenem-cilastatin)
NCT Number: NCT02149329
A multicenter open-label non-inferiority randomized clinical trial comparing the safety (non-inferiority) of short antibiotic treatment (72 hours) with an anti-pseudomonal carbapenem with regard to treatment failure in comparison with extended treatment (at least 9 days) of high-risk febrile neutropenia in hematology patients receiving standard antimicrobial prophylaxis.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
VU university medical center, Amsterdam, Netherlands
Episodes of fever are very common in patients undergoing intensive chemotherapy treatment for malignant hematological disease. More than 80% of patients experience one or more episodes of fever after their first cycle of chemotherapy. Only 20-30% of these patients have a clinically documented focus and mostly include infections of skin, intestinal tract and lung, while at most 10-25% of these patients have microbiologically proven bacteremia during these episodes. Patients with malignant hematological diseases and intensive chemotherapy induced neutropenia are extremely prone to overwhelming bacterial infections. Therefore, empirical antibiotic treatment is initiated at the first occurrence of fever, even if no apparent cause for the fever is evident. Most protocols advice treatment with very broad-spectrum antibiotics, mostly anti-pseudomonal carbapenems or fourth generation anti-pseudomonal cephalosporins.
Prolonged continuation of treatment may induce bacterial resistance. In view of the possible emergence of bacterial resistance due to prolonged antibiotic administration, continuation until recovery of neutropenia is suboptimal because it is costly because of longer hospital admissions, higher antibiotics costs and more possible adverse reactions.
Recent observational data (Slobbe et al) has showed that in adult hematological patients with febrile neutropenia, discontinuation of empiric antibacterial therapy after three days can be safe if no infectious etiology can be found, even in cases with persistent fever. However no RCT has hitherto been performed to support this observational data.
This study compares the safety (non-inferiority) of short treatment (72 hours) versus extended treatment (at least 9 days) with an anti-pseudomonal carbapenem for hematology patients with unexplained high risk febrile neutropenia. We hypothesize that a more restrictive use of broad-spectrum antibiotic use of three days in unexplained fever in neutropenic hematology patients is non-inferior to the present extended use during at least 9 days which would lead to a more restrictive use of antibiotics and less multiresistant strains of bacteria, costs and hospitalization length in the future.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Discontinuation of imipenem-cilastatin or meropenem after 3x24 hours irrespective of presence of fever.
Other names: tienam (imipenem-cilastatin)
Time frame: Between randomization (at 3x24 hours) and before 9x24hours after treatment initiation)
Treatment failure is defined as the occurrence of one of the following events after 3x24 hours and before 9x24hours after treatment initiation with a carbapenem:
-A clinically or microbiologically documented carbapenem-sensitive infection; treatment.
Recurrence of fever after previous defervescence (tympanic temperature <38.0 °C during 24 hours) which is not attributable to administration of a blood product or to a drug reaction.
o In case of clinical doubt whether the fever is of infectious etiology, the recurrence of fever will be considered as failure.
Time frame: From randomization until the end of neutropenia (neutrophil count >=0.5x10e9/L) up to 6 months after randomization.
The occurrence of death, ARDS/respiratory insufficiency, septic shock (systolic blood pressure <90 mmHg and oliguria <500 mL/day) due to any cause.
Time frame: 1. From 3x24hours of treatment until the end of neutropenia. 2. Within 30 days after the end of neutropenia
Time frame: 1. From 3x24hours of treatment until the end of neutropenia. 2.Within 30 days after recovery of neutropenia
Time frame: From admission until discharge, with an estimated average of 4 weeks
Time frame: after 3x24hours of treatment with a carbapenem and until the end of the neutropenic episode
Treatment strategy failure is defined as occurrence of any of the following events after 3x24hours of treatment with a carbapenem and until the end of the neutropenic episode:
Time frame: From the start of neutropenia (ANC<0.5x10^9) until the end of neutropenia, an expected average of 21 days
Time frame: Onset of fever until defervenscence, an expected average of 5 days.
Fever is defined as one single measured tympanic membrane temperature of >38.5°C or a temperature of >38.0°C during 2 subsequent measurements separated by at least 2 hours.
Defervescence is defined as three times a tympanic membrane temperature <37.5 °C with a minimal measurement interval of at least 8 hours
Time frame: Onset of fever until 30 days after the end of neutropenia.
Time frame: From onset of fever until 30 days after the end of neutropenia.
Time frame: From admission until discharge, with an estimated average of 4 weeks
Time frame: From the onset of fever until the end of the neutropenic episode, with an estimated average of 21 days.
Time frame: From onset of fever until 30 days after end of neutropenia.
Time frame: All previous cultures and cultures performed until 30 days after the end of neutropenia.
Time frame: om the onset of fever until the end of the neutropenic episode, with an estimated average of 21 days.
Time frame: Between 9x24hours and 14x24hours after onset of treatment with a carbapemen.
Defined as primary endpoint.
Amsterdam UMC, location VUmc
Other
Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With Fever of Unknown Origin: a Randomized Multicenter Non-inferiority Trial.
Acronym: SHORT
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