Current partner codePEPTIDESDE
NCT01754597·Not applicable·INTERVENTIONAL

Natriuretic Peptide Concentrations of B-type (BNP) During Anesthesia in Patients Previously Sensitized to Anthracyclines

Status

Completed

Phase

Not applicable

Enrollment

54

Locations

1

Results

Posted

Publications

0

Study summary

What the protocol is testing.

The cardiotoxicity of anthracyclines chemotherapy remains a major problem, despite clinical and echocardiographic monitoring. In the case of treatment for breast cancer, surgery requiring general anesthesia may follow chemotherapy. Although a possible interaction between general anesthetics and anthracyclines on systolic function is only rarely mentioned, some cases of heart failure and / or conduction disturbances peranesthésique were observed in patients treated or previously treated with anthracyclines. The determination of concentration of BNP is a diagnostic tool used in the detection of heart failure and acute coronary syndromes. The question of a possible synergism between cardiotoxic anthracyclines and anesthetic agents arises. Given its minimally invasive nature and its diagnostic value, the BNP assay might thus allow to highlight a possible subclinical deficiency. To our knowledge, there is very little data regarding a possible synergism between cardiotoxic anthracyclines and anesthetic agents.

Full detailed description

The cardiotoxicity of anthracyclines chemotherapy remains a major problem, despite clinical and echocardiographic monitoring. In the case of treatment for breast cancer, surgery requiring general anesthesia may follow chemotherapy. Although a possible interaction between general anesthetics and anthracyclines on systolic function is only rarely mentioned, some cases of heart failure and / or conduction disturbances peranesthésique were observed in patients treated or previously treated with anthracyclines. The determination of concentration of BNP is a diagnostic tool used in the detection of heart failure and acute coronary syndromes. In fact, it is one of the most sensitive markers of impaired myocardial function, and an increase in interest rates may precede any other biological changes. In a patient who received anthracycline, although it remains asymptomatic elevation of NT-proBNP concentration may persist for some months after exposure, and that, whatever the doses received. The question of a possible synergism between cardiotoxic anthracyclines and anesthetic agents arises. Given its minimally invasive nature and its diagnostic value, the BNP assay might thus allow to highlight a possible subclinical deficiency. To our knowledge, there is very little data regarding a possible synergism between cardiotoxic anthracyclines and anesthetic agents.

Interventions

Treatment arms and agents.

OTHER

Dosage of B-type natriuretic peptide (NT-proBNP)

NT-proBNP concentration assessed at the following time points : * T0: before induction of general anesthesia, NT-proBNP measurement * T1: 30 minutes after induction of general anesthesia * T2: at the end of the procedure * T3: in the postoperative period, 6 hours after the end of the procedure * T4: in the postoperative period, 24 hours after the end of the procedure

Timeline

From registration to results.

  1. First posted

    Dec 21, 2012

  2. Study start

    Sep 2009

  3. Primary completion

    Dec 2012

  4. Study completion

    Dec 2012

  5. Results posted

    Oct 1, 2025

  6. Registry updated

    Oct 1, 2025

Outcomes

What the study measures.

Primary outcomes

Pre-operative Concentration of NT-proBNP

Time frame · Before breast surgery

Mean concentration of NT-proBNP measured before surgery.

Concentration of NT-proBNP at the End of Intervention

Time frame · At the end of breast surgery

Mean concentration of NT-proBNP measured at the end of intervention

Post-operative Concentration of NT-proBNP

Time frame · 24 hours after breast surgery

Mean concentration of NT-proBNP measured 24 hours after breast surgery

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Women over 18 years with effective contraceptive method (if applicable) * NT-proBNP \<125 pg / ml * ASA 1 or 2, * Breast cancer histologically proven * Mastectomy or lumpectomy * Neoadjuvant chemotherapy with anthracyclines in 6 months or received no chemotherapy with anthracyclines, * Patients who received the briefing and signed the informed consent * Patients affiliated to a social security system. Exclusion Criteria: * Patients for whom the maintenance of general anesthesia does not use halogenated. * Renal impairment: Creatinine clearance \<60 ml / min, * Patients who for reasons psychological, social, family or geographical could not be treated or monitored regularly according to the criteria of the study, patients deprived of liberty or under guardianship. * Presence of a cardiopathy * Pregnant Women

Study locations

1 registered sites.

France. Showing up to 24 locations stored in the fast local snapshot.

Institut Bergonié

Bordeaux, Aquitaine, France

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

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