Relative interleukin-6 (IL-6) thresholds (% increase from baseline within 24 hours and % decrease from the peak postoperative value) may predict infectious and non-infectious complications after pulmonary surgery better than perioperative levels of…
ID
Bron
Verkorte titel
Aandoening
pulmonary surgery, cancer, postoperative complications
longchirurgie, kanker, postoperatieve complicaties
Ondersteuning
St. Antonius Hospital
Roche
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary endpoint is the development of an infectious complication which is defined as one of the following outcomes within 30 days of surgery:<br>
<br>
- pneumonia (purulent sputum, positive sputum or blood culture and clinical symptoms such as cough, fever or consolidation on chest radiograph)<br>
- pulmonary empyema (pleural effusion and the presence of pus on pleural aspiration, microorganism on pleural fluid culture or positive pleural fluid Gram stain)<br>
- sepsis (qSOFA score ≥2 in response to an infection)<br>
- wound infection (purulent drainage from superficial incision or deliberate opening of superficial incision by surgeon and pain, tenderness, swelling or redness)<br>
- urinary tract infection (urinary tract symptoms or fever and urine culture with no more than 2 species of organisms identified with at least one of which is a bacterium of ≥105 CFU/ml)
Achtergrond van het onderzoek
Rationale: Up to half of patients undergoing pulmonary surgery for cancer suffer from complications such as pneumonia, sepsis and mortality. Early detection of complications may improve postoperative outcome.
Objective: To identify relative interleukin-6 (IL-6) thresholds (% increase from baseline within 24 hours and % decrease from the peak postoperative value) for predicting infectious, non-infectious and any complications after pulmonary surgery and to compare the diagnostic accuracy of relative IL-6 levels for predicting postoperative complications with other biomarkers.
Study design: Multicentre prospective observational cohort study.
Study population: 250 patients undergoing elective pulmonary surgery (pneumonectomy, (bi)(sleeve)lobectomy, segmentectomy for cancer with an American Society of Anesthesiologists (ASA) physical status classification ≥2.
Intervention: None.
Main study parameters/endpoints: The main study parameters are perioperative levels of interleukin (IL-6), C-reactive (CRP), leucocyte count, procalcitonin (PCT), pro brain natriuretic peptide (proBNP), growth differentiation factor-15 (GDF-15) and high-sensitive cardiac troponin (hs-cTn). Primary endpoint is the occurrence of an infectious complication. Secondary endpoints are non-infectious complications, any complication (a composite of infectious and non-infectious complications), length of Intensive Care Unit and length of hospital stay.
Doel van het onderzoek
Relative interleukin-6 (IL-6) thresholds (% increase from baseline within 24 hours and % decrease from the peak postoperative value) may predict infectious and non-infectious complications after pulmonary surgery better than perioperative levels of C-reactive (CRP), leucocyte count, procalcitonin (PCT), pro brain natriuretic peptide (proBNP), growth differentiation factor-15 (GDF-15) and high-sensitive cardiac troponin (hs-cTn).
Onderzoeksopzet
Blood samples are drawn on the day of surgery immediately after induction of anesthesia and after 6, 9, 12 and on the morning of the first, second and third postoperative day.
Onderzoeksproduct en/of interventie
none
Algemeen / deelnemers
T. Rettig
Molengracht 21
Breda 4818 CK
The Netherlands
+31 76 595 5637
trettig@amphia.nl
Wetenschappers
T. Rettig
Molengracht 21
Breda 4818 CK
The Netherlands
+31 76 595 5637
trettig@amphia.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Elective pulmonary surgery (pneumonectomy, (bi)(sleeve)lobectomy, segmentectomy) for cancer, American Society of Anesthesiologists (ASA) physical status classification ≥2 with a planned postoperative admission to the Intensive Care.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
(suspected) Infection at the time of surgery and reoperation within 24 hours of surgery will be excluded from the study.
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL7172 |
| NTR-old | NTR7363 |
| CCMO | NL2017.20.9.1 |