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DOI: 10.1055/s-0041-109703
Ergebnisse der stadienadaptierten chirurgischen Therapie von Pleuraempyemen
Outcomes of Stage-Adapted Surgical Treatment of Pleural EmpyemaPublikationsverlauf
Publikationsdatum:
10. Februar 2016 (online)
Zusammenfassung
Hintergrund: Die chirurgische Therapie von Pleuraempyemen sollte stadien- und patientenadaptiert erfolgen. Zielsetzung der Studie war die Auswertung der Behandlungsergebnisse der chirurgischen Therapie von Patienten mit einem Pleuraempyem. Patienten und Methoden: Retrospektive Analyse aller zwischen 01/2008 und 12/2013 chirurgisch therapierten Patienten mit Pleuraempyem. Primärer Endpunkt der Studie war die stationäre Letalität. Sekundäre Endpunkte waren die stationäre Aufenthaltsdauer, die Therapieart (chirurgisch/konservativ), der Erregernachweis sowie Art, Wechsel und Dauer der Antibiotikatherapie. Ergebnisse: Von 359 Patienten hatten 0,8 % (n = 3) ein Pleuraempyem im Stadium I, 50,4 % (n = 181) ein Stadium II und 48,7 % (n = 175) ein Stadium III. Zu den am häufigsten vorkommenden Ursachen (32,4 %) zählten eine akute Pneumonie (parapneumonisches Pleuraempyem), eine (zumeist thoraxchirurgische) Operation in 18,0 % und eine abgelaufene Pneumonie (postpneumonisches Pleuraempyem) in 15,4 %. Eine Operation erfolgte in 86 % der Fälle (OP-Verfahren: offene Thorakotomie 85 %, VATS15 %). Der stationäre Aufenthalt betrug im Stadium II und III durchschnittlich 20 Tage. Die Ausheilung nach VATS war im Stadium II signifikant kürzer im Vergleich zur Thorakotomie (p = 0,022). Die Krankenhausletalität umfasste 7,0 % (25 Patienten). Im Stadium II lag die Letalität bei 5,5 % (10/185), im Stadium III bei 8,6 % (15/175). Patienten mit Erregernachweis hatten mit 9,8 % über alle Stadien eine deutlich schlechtere Letalitätsrate als Patienten ohne Erregernachweis (4,0 %; p = 0,034). Alter, maligne Grunderkrankung, Multimorbidität, Immunsuppression, Wechsel der Antibiose sowie Sepsis stellten signifikante Risikofaktoren dar. Schlussfolgerung: Die stationäre Letalität von Patienten mit einem Pleuraempyem korreliert mit dem Stadium. Positiver Erregernachweis, Sepsis, höheres Alter, Multimorbidität, eine maligne Tumorerkrankung, Immunsuppression und Antibiotikawechsel sind negative Prognosefaktoren.
Abstract
Background: The surgical treatment of pleural empyema should be carried out depending on the stage of the disease and the patientʼs symptoms. The aim of this study was to evaluate the outcomes of surgical pleural empyema treatment. Patients and Methods: Retrospective analysis of all patients with pleural empyema treated surgically between January 2008 and December 2013. The primary endpoint of the study was inpatient lethality. Secondary endpoints included duration of inpatient stay, type of treatment (surgical/conservative), proof of pathogen and type, alteration and duration of antibiotic therapy. Results: Of 359 patients, 0.8 % (n = 3) had stage I empyema, 50.4 % (n = 181) had stage II and 48.7 % (n = 175) had stage III. The most frequent causes (32.4 %) included acute pneumonia (parapneumonic pleural empyema), surgery (usually thoracic) in 18.0 % of cases and previous pneumonia (postpneumonic pleural empyema) in 15.4 %. Surgery was performed in 86 % of cases (operative procedures: open thoracotomy 85 %, VATS 15 %). The average duration of inpatient stay was 20 days for stages II and III. Recovery following VATS was significantly shorter in stage II compared to thoracotomy (p = 0.022). Hospital lethality amounted to 7.0 % (25 patients). The lethality rate was 5.5 % (10/185) in stage II and 8.6 % (15/175) in stage III. Patients with confirmed pathogens had a significantly worse mortality rate across all stages (9.8 %) than patients with no confirmed pathogens (4.0 %, p = 0.034). Age, malignant underlying disease, multiple comorbidities, immunosuppression, a change in antibiotic regimens and sepsis were significant risk factors. Conclusion: The inpatient lethality of patients with pleural empyema correlates with the stage of the condition. Positive confirmation of pathogens, sepsis, a higher age, multiple comorbidities, malignant tumour disease, immunosuppression and a change of antibiotics are negative prognostic factors.
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