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Neutropenic fever is a life threatening condition that is not rare in patients suffering from hematologic disorders, and of paramount importance to early and effective treatment. In this trial we concentrate on hospitalized patients with hematologic malignancies who develop neutropenic fever.
In recent years, several studies were conducted to examine possible changes in the conventional empirical treatment, assuming that administration of the antibiotics in a prolonged infusion would allow for a greater fT > MIC that will lead to a better efficacy.
These studies were carried out in different populations and there is only limited information about the importance of continuous infusion therapy in patients with hematologic diseases with neutropenic fever.
Research goals: The main goal is to compare between two groups of hematologic patients with neutropenic fever, The first group will receive antibiotic therapy in extended infusion, and the second (control) group will receive the treatment in a fixed time.
METHODS: Each patient who will be hospitalized in the Department of Bone Marrow Transplantation and which meets the Inclusion criteria for, will be offered to participate in the study. If fever appears during hospitalization empirical treatment of neutropenia will be initiated performed in accordance with the allocation of the patient in the study. Therapeutic success is defined as a combination of several clinical parameters, including: a decline in Fever, the recurrence of fever and improvement in infection.
METHODS: Study format - Prospective unblinded randomized trial.
Neutropenic fever measurement will be set above the fold of 38.3 ° C or fever over 38.0 ° C lasting more than an hour. Neutropenia is defined as absolute neutrophil count (ANC) less than 500 cells / mm3, or expected to fall below this value for the next 48 hours.
Primary care would be one of three options:
Supplementation of Vancomycin will be at the discretion of the treating physician.
Antibiotic therapy will be replaced, in coordination with the Department of Infectious Diseases in the following cases:
Replacement of antibiotic therapy is defined as a failure as defined by the primary endpoint. In such a case, continued treatment of the patient would be according to the BMT unit protocol for treatment for neutropenic fever.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prolonged Infusion of antibiotics | Experimental | Prolonged (4 hours) Infusion of antibiotics. Intervention: Primary care would be one of three options:
Supplementation of Vancomycin will be at the discretion of the treating physician. |
|
| Fixed time infusion of antibiotics | Active Comparator | Fixed time (half and hour) infusion of antibiotics. Intervention: Primary care would be one of three options:
Supplementation of Vancomycin will be at the discretion of the treating physician/ |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Piperacillin/tazobactam | Drug | Initial treatment will be with Piperacillin + Tazobactam |
|
| Measure | Description | Time Frame |
|---|---|---|
| A successful response to treatment | A successful response to treatment will be defined by a combination of all the following: A. A defervescence of fever for at least 48 hours. B. Disappearance or improvement of clinical signs and symptoms of infection. C. No: bacteremia / re-emergence of fever / signs of infection within 5 days from starting of treatment. | Interim analysis is planed after 1 year , when a recruitment of 50 patients is expected |
| Measure | Description | Time Frame |
|---|---|---|
| Breakthrough fever or Additional bacteremia | 5 days after primary treatment | |
| Clostridium difficile infection | For the duration of hospital stay - an expected average of 4 weeks | |
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Inclusion Criteria:
Patients who are able to sign an informed consent form
Hospitalized patients for one of the following reasons:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ron Ram, MD | Contact | +972-3-6974138 | ronr@tlvmc.gov.il | |
| Ronen Ben-Ami, MD | Contact | +972-3-6974347 | ronenba@tlvmc.gov.il |
| Name | Affiliation | Role |
|---|---|---|
| Dr. Ron Ram, MD | Head of BMt Unit / hematology division | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Tel-Aviv Sourasky Medicak center / BMT Unit | Tel Aviv | 6423906 | Israel |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29608680 | Derived | Ram R, Halavy Y, Amit O, Paran Y, Katchman E, Yachini B, Kor S, Avivi I, Ben-Ami R. Extended vs Bolus Infusion of Broad-Spectrum beta-Lactams for Febrile Neutropenia: An Unblinded, Randomized Trial. Clin Infect Dis. 2018 Sep 28;67(8):1153-1160. doi: 10.1093/cid/ciy258. |
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| ID | Term |
|---|---|
| D005334 | Fever |
| D064147 | Febrile Neutropenia |
| ID | Term |
|---|---|
| D001832 | Body Temperature Changes |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009503 | Neutropenia |
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| ID | Term |
|---|---|
| D000077725 | Piperacillin, Tazobactam Drug Combination |
| D002442 | Ceftazidime |
| D000077731 | Meropenem |
| D014640 | Vancomycin |
| ID | Term |
|---|---|
| D000078142 | Tazobactam |
| D010397 | Penicillanic Acid |
| D010406 | Penicillins |
| D047090 | beta-Lactams |
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|
| Ceftazidim | Drug | Patient with sensitivity to penicillin will receive Ceftazidim |
|
|
| Meropenem | Drug | In cases of hypotension that do not respond to fluids resuscitation , and in consultation with the infectious diseases unit - we will start empirical treatment with Meropenem |
|
|
| Vancomycin | Drug | Supplementation of Vancomycin will be at the discretion of the treating physician |
|
|
| Survival |
| During 30 days from begining of treatment |
| Duration of Hospitalization | For the duration of hospital stay - an expected average of 4 weeks |
| Number of days of Neutropenia | For the duration of hospital stay - an expected average of 4 weeks |
| Any systemic organ Failure (Renal / Hepatic / Cardio or pulmonary) | For the duration of hospital stay - an expected average of 4 weeks |
| D000380 | Agranulocytosis |
| D007970 | Leukopenia |
| D000095542 | Cytopenia |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007960 | Leukocyte Disorders |
| D007769 |
| Lactams |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D010878 | Piperacillin |
| D000667 | Ampicillin |
| D010400 | Penicillin G |
| D013457 | Sulfur Compounds |
| D013450 | Sulfones |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |
| D002509 | Cephaloridine |
| D002511 | Cephalosporins |
| D013843 | Thiazines |
| D013845 | Thienamycins |
| D015780 | Carbapenems |
| D006020 | Glycopeptides |
| D006001 | Glycoconjugates |
| D002241 | Carbohydrates |
| D010455 | Peptides |
| D000602 | Amino Acids, Peptides, and Proteins |