Pediatric/Congenital/DevelopmentalAntibiotic utilization based on primary treatment of pediatric empyema
Introduction
The treatment of pediatric empyema has undergone a significant transformation over the course of the past decade. Mechanical debridement was originally performed by thoracotomy, progressing to a minimally invasive approach via video-assisted thoracoscopic surgery (VATS). When compared to a thoracostomy tube, VATS resulted in a more timely and thorough resolution of the pleural space disease [1]. However, practitioners have begun injecting tissue plasminogen activator (tPA) via the thoracostomy tube, which results in disruption of the tissue loculations leading to adequate drainage. Two randomized studies comparing mechanical debridement (VATS) and chemical debridement (tPA or urokinase) found no difference in the length of hospitalization or other outcome parameters except surgical debridement was more expensive [2], [3].
No studies have been completed evaluating the appropriate length of antibiotic therapy for empyema. The current recommendation is a 10-d course once afebrile [1]. However, this is a grade D recommendation and traditionally, patients have continued antimicrobial therapy much longer. One study found an average parenteral antibiotic duration of 24 d although fever abated by 9 d raising the concern that increased duration of therapy could contribute to bacterial resistance [4]. A recent survey of infectious disease experts failed to reach a consensus on antibiotic selection or duration for empyema. Thirty-five percent recommended 11–14-d treatment, 41% advised 15–21 d, and 17% recommended >21 d [5]. We sought to assess the current medical treatment of empyema in our institution to help establish an evidence-based treatment protocol.
Section snippets
Methods
We performed a retrospective analysis on children with empyema who underwent chemical and/or mechanical fibrinolysis after institutional review board approval (14070291). Inclusion criteria were age <18 y and diagnosis of empyema requiring chemical or mechanical debridement between 2005 and 2013. In our center, triggers for definitive therapy include septations or loculations in the pleural space visualized on imaging or patients with pleural fluid containing white blood cell count >10,000
Results
A total of 179 patients were identified and 169 included in the analysis. Ten patients were excluded, including those with immunocompromised state (n = 4), additional sites of infection (n = 5), or both (n = 1). Demographics revealed a mean age (±standard deviation) of 6.2 ± 4.8 y. There were 78 females (46%) and 91 males (54%; Table 1). The average days of symptoms before admission were 7.3 ± 4.3 d. There were 1.8 ± 1.2 visits to a pediatrician, emergency department, or outside hospital before
Discussion
Most pediatric empyema cases are due to S pneumoniae; however, even with the emergence of heptavalent protein-polysaccharide conjugate vaccine, the incidence of empyema in children under two doubled after its release; the rates among children aged 2–4 nearly tripled [6], prompting development of a 13-valent pneumococcal vaccine in 2010. Since that time there has been evidence that complicated pneumococcal pneumonia may be declining [7]. Our study included patients treated for empyema both
Conclusions
Patients diagnosed with empyema are currently placed on a protracted and variable time course of antibiotic therapy, which seems to be influenced by primary treatment and the presence of necrosis or abscess. Because nearly half of our population experienced side effects from antimicrobial therapy, a standardized protocol with truncated duration of treatment should be used, which will reduce variability, duration of therapy, and costs.
Acknowledgment
Authors' contributions: K.W.G., B.G.A.D., and S.D.S.P. contributed to the literature search. K.W.G., B.G.A.D., A.L.M., J.G.N., and S.D.S.P. did the study design. K.W.G. and B.G.A.D. did the data collection. K.W.G. and S.D.S.P. did the analysis, interpretation, and writing. K.W.G., A.L.M., J.G.N., and S.D.S.P. did the critical revision.
References (15)
- et al.
The diagnosis and management of empyema in children: a comprehensive review from the APSA Outcomes and Clinical Trials Committee
J Pediatr Surg
(2012) - et al.
Thoracoscopic decortication vs tube thoracostomy with fibrinolysis for empyema in children: a prospective randomized trial
J Pediatr Surg
(2009) - et al.
Experience with an evidence-based protocol using fibrinolysis as first line treatment for empyema in children
J Pediatr Surg
(2013) - et al.
Evaluating the quality of antimicrobial prescribing: is standardisation possible?
Enferm Infecc Microbiol Clin
(2013) - et al.
Variation in antibiotic use in the European Union
Lancet
(2001) - et al.
Complicated parapneumonic effusion and empyema in children
J Microbiol Immunol Infect
(2006) - et al.
Variability in pediatric infectious disease consultants’ recommendations for management of community-acquired pneumonia
PLoS One
(2011)
Cited by (7)
Surgical management of complications of burn injury
2018, Total Burn Care: Fifth EditionSurgical Management of Complications of Burn Injury
2017, Total Burn Care, Fifth EditionGuidelines for the Management of Respiratory Infectious Diseases in Children in Japan 2022
2023, Pediatric Infectious Disease JournalProtocol-driven Antibiotic Treatment of Pediatric Empyema After Fibrinolysis
2021, Pediatric Infectious Disease JournalInternational survey of paediatric infectious diseases consultants on the management of community-acquired pneumonia complicated by pleural empyema
2019, Journal of Paediatrics and Child HealthBLOOD CULTURE AND PLEURAL FLUID CULTURE YIELDS IN PEDIATRIC EMPYEMA PATIENTS A Retrospective Review, 1996–2016
2018, Pediatric Infectious Disease Journal