Skip to main content

Medical thoracoscopy treatment for pleural infections: a systematic review and meta-analysis

Abstract

Background

Complicated parapneumonic effusions and empyema represent advanced stages of pleural infections and are characterized by a high mortality. Medical thoracoscopy is a safe and minimally invasive endoscopic technique prescribed to treat severe pleural infections. However, only a few studies evaluated its success rate. A systematic review of observational studies was performed to assess the efficacy of medical thoracoscopy in patients with complicated parapneumonic effusions and empyema, as well as its predictive factors.

Methods

A search of the scientific evidence was carried out using PubMed, EMBASE, and Cochrane Central Register of Controlled Trials. Articles describing observational studies on medical thoracoscopy in patients with parapneumonic effusions and empyema were selected.

Results

Eight studies met the inclusion criteria. The pooled treatment success rate of thoracoscopy was 85% (95% CI 80.0–90.0%; I2: 61.8%) when used as first-line intervention or after failure of chest tube. The pooled complication rate was 9.0% (95% CI 6.0–14.0%; I2: 58.8%). A pooled difference of treatment success of 9.0% (95% CI 1.0–18.0%) was found when post-thoracoscopy intra-pleural fibrinolysis was prescribed. Pooled success rate was higher in cases with pleural fluid culture negativity (pooled difference: 14.0%; 95% CI 4.0–24.0%).

Conclusions

Medical thoracoscopy is effective and safe when prescribed for complicated parapneumonic effusions and empyema. Bacteriological negativity of pleural effusion specimens and administration of adjuvant intra-pleural fibrinolysis after the procedure are associated with a higher success rate.

Peer Review reports

Background

Pleural infections are highly incident medical conditions, which frequently complicate both community- and healthcare-associated pneumonia [1,2,3].

Complicated parapneumonic effusion (CPE) (i.e., pleural infection with at least one of the following criteria: pH < 7.2, LDH > 1000 IU/l or glucose < 60 mg/dL) and empyema (i.e., pus in the pleural space or positive gram stain/culture for pathogenic organisms) represent advanced stages of disease, characterized by high mortality [2,3,4,5].

International guidelines suggest antibiotic therapy and early drainage of the pleural space by chest tube; surgery may be recommended when patients fail medical therapy and/or in case of organized empyema with extensive pleural fibrosis requiring decortication [4, 6].

Medical thoracoscopy (i.e., thoracoscopy performed with local anaesthesia under conscious sedation) is a safe and minimally invasive endoscopic technique, which is prescribed for several pleural diseases (e.g. diagnosis of pleural effusions of unknown aetiology or suspected for malignancy, talc poudrage pleurodesis in pleural neoplasms and pneumothorax) [7,8,9]. It shows several advantages if compared with conventional medical therapy, particularly in cases of multi-loculated pleural effusion [7,8,9]. Indeed, it can mechanically disrupt fibrin adhesions, can help position chest tubes under direct vision and perform pleural biopsy [7,8,9]. Current guidelines do not recommend its use for the above-mentioned indications, following the absence of any evidence from randomized controlled trials on the efficacy in the management of pleural infections [4, 7].

A limited number of studies specifically assessed the therapeutic success of medical thoracoscopy in cases of CPE and empyema [10,11,12,13,14,15,16,17,18].

The aim of the present systematic review was to describe the findings of the available scientific evidence in order to provide a pooled estimate of therapeutic efficacy of medical thoracoscopy in CPE and empyema, and to identify the main predictive factors of a successful procedure.

Methods

Search strategy

Observational studies on the therapeutic use of medical thoracoscopy in patients with CPE and empyema were searched in the search engines PubMed, Cochrane Central Register of Controlled Trials, and EMBASE, from their inception to 30th June 2020.

To retrieve the scientific evidence from the above-mentioned databases strings were created using the following single and combined key-words: “thoracoscopy”, “medical thoracoscopy”, “empyema”, “complicated parapneumonic effusion”, “loculated parapneumonic effusion”, “CPE”, “pleural infection”, and “pleural effusion”.

Reviews on this topic or similar topics, as well as their list of references, were carefully evaluated to identify pertinent manuscripts.

Conference proceedings and abstracts of national and international congresses were basically excluded being unreliable for the poor information provided in the methods and in the results sections.

The systematic review was registered at PROSPERO with the number CRD42018096193.

Study selection

The selected epidemiological studies were aimed at evaluating the therapeutic efficacy of medical thoracoscopy in patients with CPE or empyema, as well as the risk factors associated with a successful intervention.

Articles were excluded based on one of the following criteria: (1) unclear primary and secondary outcomes; (2) thoracoscopy adopted for diagnostic purposes; (3) studies performed in animals; (4) case-reports or case-series which enrolled less than 10 patients; (5) editorials, correspondences, reviews; (6) languages other than English; (7) observational studies evaluating thoracoscopy for the treatment of complicated parapneumonic effusions and empyema performed with general anesthesia and/or endotracheal intubation and/or involving other type of anesthesia different from local anesthesia; 8) experimental studies.

Two Authors (L.S. and F.T.) carefully and independently evaluated titles and abstracts of the records for the selection of the full texts, which were assessed for their eligibility by the same Authors.

Discrepancies during the selection of the articles and extraction of the variables were solved by the intervention of a third Author (G.S.).

Data extraction

Qualitative and quantitative variables were collected in an ad hoc electronic form.

The following variables were collected: first author of the article; title of the article; year when the study was published; year/s when the study was conducted; epidemiological study design; country/ies where the study was carried out; sample size; age; gender; therapeutic thoracoscopy for empyema; microbiological diagnosis; diagnosis of tuberculosis (TB); etiology of pleural effusion; treatment success; tube duration; assessment of successful intervention; complications of medical thoracoscopy; mortality; type of radiological screening; radiological findings; pleural infection stage; type of intra-pleural fibrinolytic therapy (IPFT); duration of symptoms; entry points; type of thoracoscope; tool adopted for fibrinous septae disruption; chest tube; post-procedure negative pressure suction.

Data independently extracted by the above-mentioned Authors were cross-checked for the detection of inconsistencies. The inter-rater agreement was ~ 100% because no significant discrepancies were found.

No ethical approval was requested to the ethical committee because anonymized and aggregated data were retrieved from the selected articles.

Study quality assessment

Inter-rated agreement was ~ 100% for the phases of study selection and data extraction and the few inconsistencies were solved by consensus and with the support of a third senior Author (G.S.).

Guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) were followed to guide the process of the systematic review and meta-analysis.

The scientific quality of the observational studies was evaluated according to the Scottish Intercollegiate Guidelines Network.

Statistical analysis

A descriptive analysis of the qualitative and quantitative variables was carried out: absolute and relative (percentage) frequencies and means (range) were used to summarize qualitative and quantitative variables, respectively.

Forest plots were used to describe between-study variability of point and interval (95% confidence interval, CI) estimates, as well as the weight of the sample size of recruited studies. Pooled and heterogeneity indicators were adopted to summarize key study variables. The I2 indicator (low, medium, and high heterogeneity expressed as < 25%, ≥ 25–< 50%, ≥ 50%, respectively) showed the association between true variability and overall variation.

Fixed and random-effects models were chosen depending on the between-study heterogeneity.

Publication bias was graphically evaluated with bias assessment plots, as well as with the Egger weighted regression test. A two-tailed p value less than 0.05 was deemed statistically significant. The statistical softwares were Stata version 16 (StatsCorp, Texas, USA) and StatsDirect version 3.1.12 (StatsDirect Ltd).

Results

Study selection

The search of the electronic databases found 7,922 records (Fig. 1). A total of eight studies were selected for the qualitative and quantitative analysis; 200 studies were excluded for the following reasons: other topics (n = 74), only abstract available (n = 71), reviews (n = 17), case-reports (n = 8), case-series with less than ten patients (n = 7), Video Assisted Thoracoscopic Surgery (VATS) (n = 8), letters (n = 5), editorials (n = 3), articles written in languages than English (n = 3), randomized controlled trials (n = 1), studies without any results (n = 2), and full-text not available (n = 1).

Fig. 1
figure1

PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) 2009 flow diagram

Characteristics of the selected studies

The articles describe studies carried out between 1989 [11] and 2016 [15, 17]. They were published between 1997 [10] and 2018 [17] (Table 1).

Table 1 Summary of the included studies

The following countries were involved in the selected studies: Switzerland (2, 22.2%) [10, 11], Italy (2, 22.2%)[11, 12], Japan (1, 11.1%) [13], China (1, 11.1%) [14], Egypt (1, 11.1%) [15], UK (1, 11.1%) [16], Greece (1, 11.1%)[16], and Pakistan (1, 11.1%)[17]. Studies were mono-center in most of the cases (6, 66.7%) [10, 12,13,14,15, 17], whereas multi-center in only two (25%)[10, 16] studies. Three (33.3%) [10, 13, 17] case-series recruiting ≥ 10 patients were selected; five (62.5%) [11, 12, 14,15,16] studies were observational and retrospective, without providing further epidemiological details.

Characteristics of the study samples

Sample size of the selected studies ranged from 16 [10] to 430 [14] patients (Table 1). The majority of the studies (7, 77.8%) [10, 12, 13, 15,16,17] described the use of thoracoscopy for the management of empyema, whereas one article described this scope of thoracoscopy only in 15.1% [14] of their patients.

The mean (range) age of the recruited patients in a single study was 51.7 (6–93[9, 10, 12]) years. The proportion of males in every single research ranged from 62.5 [9] to 82.9% [12].

Microbiological diagnosis was carried out in 100% of the patients in only two (22.2%) [14, 17] studies; however, in two (25%) studies the proportion was less than 50% (i.e., 45.7% [11], and 40.0% [15]) (Additional file 1: Table S1). TB diagnosis was performed in only four (44.4%) [11, 12, 14, 17] studies. Infections caused by Gram-positive and -negative bacteria were found in 5 (55.6%) [10,11,12,13, 15] and 5 (55.6%) [10,11,12,13, 15] studies, respectively. The proportion of infections caused by Gram-positive bacteria in every study ranged from 9.8 [12] to 41.4% [13], whereas the proportion of infections caused by Gram-negatives varied from 7.9 [11] to 14.6% [12].

A diagnosis of malignancy in empyema specimens was performed in four (44.4%) [11, 13, 15, 17] studies: the percentage of cases ranged from 0.3 [15] to 12.5% [17].

Treatment success rate was described in all selected studies [10,11,12,13,14,15,16,17,18]: it varied from 75.0 [10] to 94% [17] (Table 2). Pooled treatment success rate was 85% (95% CI 80.0–90.0%; I2: 61.8%) (Fig. 2). Pooled treatment success rate in Gram-positive and -negative infections was 74.0% (95% CI 61–86%; I2: 16.1%) and 77.0% (95% CI 54.0–93.0%; I2: 0.0%) respectively. Definition of success depended on the absence of further surgical interventions in four (50%) [9, 10, 14, 16] studies. Other three (33.3%) [12, 13, 17] studies defined a successful thoracoscopy based on a radiological resolution and objective evidence of sepsis resolution; one (11.1%) [15] study defined the technique successful following clinical and radiological improvement (Table 2).

Table 2 Main outcomes of the included studies
Fig. 2
figure2

Treatment success rate of medical thoracoscopy in complicated parapneumonic effusion and empyema

Complications were described by seven (77.8%) [11,12,13,14,15,16,17] studies: the rate of complications ranged from 3.1 [14] to 26.7% [15] (Table 3). Pooled complication rate was 9.0% (95% CI 6.0–14.0%; I2: 58.8%). The most frequent adverse event was air leakage: it was reported by three (33.3%) studies [11, 16, 17].

Table 3 Complications following medical thoracoscopy

Chest x-ray and CT scan were adopted to screen the intervention in 1 (11.1%) [13] study, whereas one (11.1%) [12] study used CT scan and chest ultrasounds (Additional file 1: Table S2). Two (22.2%) [10, 11] studies reported the use of only ultrasonography, whereas four (44.4%) [14,15,16,17] studies used all radiological tools previously mentioned. The most prevalent radiological findings were multi-loculated (7, 77.8%, studies [11,12,13,14,15,16,17]), free flowing effusion (3, 33.3%, studies [12, 15, 16]), and organized effusion (2, 22.2%, studies [12, 14]). Staging of pleural infections was performed in all studies [10, 17]: empyema was described in 8 (88.9%) studies [10,11,12,13, 15,16,17], whereas complicated parapneumonic effusion in 3 (33.3%) studies [10, 13, 14].

Entry-points were described in three (37.5%) [14, 16, 17] studies: they ranged from one [14, 16, 17] to two [17]. Thoracoscopy was used as first-line intervention and after failure of chest tube in four (44.4%) [13,14,15,16] and in four (44.4%) [10,11,12, 17] studies, respectively (Table 4). The type of thoracoscope was semi-rigid [13] or rigid [9,10,11,12, 14,15,16]; only one (12.5%)[17] study did not report on the characteristics of the thoracoscope. The instrument adopted for fibrinous septae disruption was biopsy forceps in eight (88.9%) studies [10,11,12,13,14,15,16,17]. Chest tube size ranged from 20 [12] to 32 F [12, 17]. Post-procedure negative pressure suction was adopted in 6 (66.7%) studies [10,11,12,13,14, 17]. Mean (range) duration of tube positioning was 8.2 (2–18 [10, 12, 13, 16]) days, although it was reported only by five (55.6%) [10, 12,13,14, 16] manuscripts.

Table 4 Main characteristics of the thoracoscopic procedures

Three (33.3%) [11,12,13] studies evaluated the treatment success rate in patients exposed to post-thoracoscopy intra-pleural fibrinolysis: it ranged from 81.8 [13] to 96.8% [11] Brutsche et al. administered 250.000 U of streptokinase or 100,000 U of urokinase diluted in 100 ml of normal saline solution once daily during 3–5 days, in the presence of depots of fibrin after thoracoscopy [11]; Ravaglia et al. administered 100.000 U of urokinase diluted in 100 ml of saline solution once daily for 3–5 days in case of multiloculated and organized empyema [12], while Ohuchi et al. employed urokinase or fibrinolysin/deoxyribonuclease (240.000 U diluted in 40 ml of normal saline solution once daily) in case of residual spaces after thoracoscopy [13] (Additional file 1: Table S3).

Pooled difference of treatment success rate between those exposed and not exposed to fibrinolysis was 9% (95% CI 1.0–18.0%) in favour of fibrinolysis (Fig. 3). Pooled success rate was higher in those without any bacteriological detection (pooled difference 14.0%; 95% CI 4.0–24.0%) (Fig. 4).

Fig. 3
figure3

Success rate differences according to the administration of post-thoracoscopy intra-pleural fibrinolysis

Fig. 4
figure4

Success rate differences according to detection of bacteriological infection

Quality assessment found a high risk of bias in the majority of the recruited studies (8, 88.9% [10,11,12,13, 15,16,17]) (Additional file 1: Table S4).

Discussion

The present systematic review and meta-analysis provides for the first time a comprehensive description of the main results published in studies which evaluated the therapeutic efficacy of medical thoracoscopy for CPE and empyema. Overall, the pooled therapeutic success rate (85.0%) was high, and the safety profile of the technique when performed as first-line procedure or after a chest tube treatment failure was good (pooled complication rate of 9.0%). The findings are clinically relevant: the vast majority of the patients with complicated pleural infections who underwent this technique recover and do not need more invasive surgical procedures.

Predictors of high effectiveness included the negative bacteriological detection and the administration of intra-pleural fibrinolysis after the procedure.

Previous studies showed conflicting findings on the prognosis of culture-positive pleural effusions, which could be associated with a higher bacterial load [11, 18,19,20]. Brutsche et al. demonstrated a higher treatment failure of medical thoracoscopy in culture positive effusions and empyema [11]. Okikor et al. showed a longer duration of pleural drainage and hospital stay and more frequent complications in patients with culture-positive organized empyema who underwent thoracotomy and decortication, without any differences in achieving lung re-expansion [18]. Notably, Khemasuwan et al. did not prove a role of culture positivity on treatment outcomes in 84 patients with CPE/empyema treated with chest tube and intra-pleural fibrinolytic therapy [19].

Our data confirm the findings of Brutsche et al., with a higher success rate of the technique in case of culture negative pleural infections [11]. No difference in therapeutic efficacy was recorded between different germ type infections (i.e. gram positive versus gram negative) [11].

International guidelines do not suggest the routine use of IPFT in the absence of a clear benefit over placebo in terms of reduction of mortality, referral for surgery, length of hospital stay, and radiological improvement [4, 6]. They postulate their possible administration in case of symptomatic, persistent, multi-loculated pleural effusions in patients whose conditions do not allow the immediate implementation of surgical procedures (e.g., comorbidities) [4].

Notably, a more recent randomized clinical trial (i.e. MIST2 trial) and a meta-analysis showed that intrapleural fibrinolytic therapy, administered through chest tube, was associated with a reduced frequency of surgical interventions and treatment failure; however, mortality rate did not significantly change [21, 22].

A recent small randomized clinical trial, which enrolled 32 patients with pleural infections was designed to compare the length of hospital stay between medical thoracoscopy and chest tube with IPFT. It failed to detect a significant difference in therapeutic success between these techniques (75.0% vs. 81.3%, respectively). However, the study was not powered to detect a difference for this outcome [23].

Three studies described the post-thoracoscopy administration of IPFT in patients with multi-loculated pleural effusions and/or in case of persistent fibrin depots following the endoscopic procedure [11,12,13].

Pooled estimate shows a slightly higher therapeutic success after combining medical thoracoscopy and intra-pleural fibrinolytics administered after the procedure. This might suggest a potential advantage related to IPFT after the mechanical disruption of major pleural adhesions by the thoracoscopic forceps.

Half of the studies included in the present meta-analysis describe the use of thoracoscopy as first-line technique, instead of second-line therapeutic option after chest tube failure. Since this approach does not reflect the current standard of care, mainly in those patients with free-flowing pleural effusion, it may represent a limitation in changing clinical practice.

Four studies described the diagnosis of malignancy associated to empyema. Local anesthetic thoracoscopy may also play an important diagnostic role in difficult-to-treat pleural infections. Indeed, pleural biopsies help collect additional tissue samples for microbiological and histopathological examinations [11, 15, 17].

Some methodological limitations of the present review could be found.

The quality of the study design is poor: the quality assessment found a high risk of bias. The selected studies were observational and confounding factors and selection bias could hinder the reliability of the findings. Some important variables were not collected or described in the selected studies: this can under-or over-estimate some point estimates. Furthermore, standard operating procedures could be different: the available information retrieved from the individual studies cannot be sufficient to discriminate any procedural differences which can affect the findings. The timing of the procedure is not clearly defined: this important variable could explain some results described by the selected studies. Finally, several studies have adopted various definitions of treatment success for medical thoracoscopy.

Conclusions

In conclusion, this systematic review and meta-analysis shows that medical thoracoscopy is an effective and safe minimally invasive technique for the treatment of complicated parapneumonic effusion and empyema. The bacteriological negativity and the administration of adjuvant IPFT immediately after the procedure are associated with better therapeutic outcomes.

Despite the study limitations, our findings could be the scientific basis of new recommendations: current international guidelines do not suggest medical thoracoscopy in the therapeutic work-up of pleural infections.

Ongoing randomized controlled trials (ClinicalTrials.gov Identifiers: NCT03468933; NCT03859206) will directly compare cost-effectiveness of medical thoracoscopy with standard medical treatment (i.e., chest tube with and without IPFT).

The good performance and the optimal safety profile could change the therapeutic landscape of pleural infections: thoracoscopy could be the first-line technique in multi-loculated CPE and empyema, mainly in frail patients (e.g., elderly with comorbidities) who cannot undergo general anesthesia and surgical procedures [9, 12, 24].

Future studies are needed to assess the optimal timing of medical thoracoscopy in the management of advanced pleural infections.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CPE:

Complicated parapneumonic effusion

TB:

Tuberculosis

VATS:

Video assisted thoracoscopic surgery

IPFT:

Intra-pleural fibrinolytic therapy

References

  1. 1.

    Corcoran JP, Wrightson JM, Belcher E, DeCamp MM, Feller-Kopman D, Rahman NM. Pleural infection: past, present, and future directions. Lancet Respir Med. 2015;3(7):563–77.

    Article  Google Scholar 

  2. 2.

    Falguera M, Carratalà J, Bielsa S, García-Vidal C, Ruiz-González A, Chica I, et al. Predictive factors, microbiology and outcome of patients with parapneumonic effusion. Eur Respir J. 2011;38(5):1173–9.

    CAS  Article  Google Scholar 

  3. 3.

    Chalmers JD, Singanayagam A, Murray MP, Scally C, Fawzi A, Hill AT. Risk factors for complicated parapneumonic effusion and empyema on presentation to hospital with community-acquired pneumonia. Thorax. 2009;64(7):592–7.

    CAS  Article  Google Scholar 

  4. 4.

    Davies HE, Davies RJ, Davies CW, British Thoracic Society Pleural Disease Guideline Group. Management of pleural infection in adults: British Thoracic Society Pleural Disease Guideline 2010. Thorax. 2010;65(Suppl 2):ii41–53.

    Article  Google Scholar 

  5. 5.

    Light RW, Girard WM, Jenkinson SG, George RB. Parapneumonic effusions. Am J Med. 1980;69(4):507–12.

    CAS  Article  Google Scholar 

  6. 6.

    Shen KR, Bribriesco A, Crabtree T, Denlinger C, Eby J, Eiken P, et al. The American Association for Thoracic Surgery consensus guidelines for the management of empyema. J Thorac Cardiovasc Surg. 2017;153(6):e129–46.

    Article  Google Scholar 

  7. 7.

    Rahman NM, Ali NJ, Brown G, Chapman SJ, Davies RJ, Downer NJ, et al. Local anaesthetic thoracoscopy: British Thoracic Society Pleural Disease Guideline 2010. Thorax. 2010;65(Suppl 2):ii54–60.

    Article  Google Scholar 

  8. 8.

    Carlucci P, Trigiani M, Mori PA, Mondoni M, Pinelli V, Casalini AG, et al. Competence in pleural procedures. Panminerva Med. 2019;61(3):326–43.

    Article  Google Scholar 

  9. 9.

    Bedawi EO, Hassan M, Rahman NM. Recent developments in the management of pleural infection: a comprehensive review. Clin Respir J. 2018;12(8):2309–20.

    Article  Google Scholar 

  10. 10.

    Solèr M, Wyser C, Bolliger CT, Perruchoud AP. Treatment of early parapneumonic empyema by “medical” thoracoscopy. Schweiz Med Wochenschr. 1997;127(42):1748–53.

    PubMed  Google Scholar 

  11. 11.

    Brutsche MH, Tassi GF, Györik S, Gökcimen M, Renard C, Marchetti GP, Tschopp JM. Treatment of sonographically stratified multiloculated thoracic empyema by medical thoracoscopy. Chest. 2005;128(5):3303–9.

    Article  Google Scholar 

  12. 12.

    Ravaglia C, Gurioli C, Tomassetti S, Casoni GL, Romagnoli M, Gurioli C, et al. Is medical thoracoscopy efficient in the management of multiloculated and organized thoracic empyema? Respiration. 2012;84(3):219–24.

    Article  Google Scholar 

  13. 13.

    Ohuchi M, Inoue S, Ozaki Y, Fujita T, Igarashi T, Ueda K, Hanaoka J. Single-trocar thoracoscopy under local anesthesia for pleural space infection. Gen Thorac Cardiovasc Surg. 2014;62(8):503–10.

    Article  Google Scholar 

  14. 14.

    Xiong Y, Gao X, Zhu H, Ding C, Wang J. Role of medical thoracoscopy in the treatment of tuberculous pleural effusion. J Thorac Dis. 2016;8(1):52–60.

    PubMed  PubMed Central  Google Scholar 

  15. 15.

    Abo-El-maged AHA, Elsamadony MF, El-Shamly MM, Hablas WR. Safety and efficacy of medical thoracoscopy in the management of loculated thoracic empyema. Egypt J Chest Dis Tuberc. 2017;66(3):445–51.

    Article  Google Scholar 

  16. 16.

    Hardavella G, Papakonstantinou NA, Karampinis I, Papavasileiou G, Ajab S, Shafaat M, et al. Hippocrates quoted “If an Empyema Does Not Rupture, Death Will Occur”: is medical thoracoscopy able to make it rupture safely? J Bronchology Interv Pulmonol. 2017;24(1):15–20.

    Article  Google Scholar 

  17. 17.

    Sumalani KK, Rizvi NA, Asghar A. Role of medical thoracoscopy in the management of multiloculated empyema. BMC Pulm Med. 2018;18(1):179.

    Article  Google Scholar 

  18. 18.

    Okikor L, Coltart C, Bille A, Guile L, Pilling J, Harrison-Phipps K, et al. Thoracotomy and decortication: impact of culture-positive empyema on the outcome of surgery. Eur J Cardiothorac Surg. 2014;46(5):901–6.

    Article  Google Scholar 

  19. 19.

    Khemasuwan D, Sorensen J, Griffin DC. Predictive variables for failure in administration of intrapleural tissue plasminogen activator/deoxyribonuclease in patients with complicated parapneumonic effusions/empyema. Chest. 2018;154(3):550–6.

    Article  Google Scholar 

  20. 20.

    Godfrey MS, Bramley KT, Detterbeck F. Medical and surgical management of empyema. Semin Respir Crit Care Med. 2019;40(3):361–74.

    Article  Google Scholar 

  21. 21.

    Rahman NM, Maskell NA, West A, Teoh R, Arnold A, Mackinlay C, et al. Intrapleural use of tissue plasminogen activator and DNase in pleural infection. N Engl J Med. 2011;365(6):518–26.

    CAS  Article  Google Scholar 

  22. 22.

    Altmann ES, Crossingham I, Wilson S, Davies HR. Intra-pleural fibrinolytic therapy versus placebo, or a different fibrinolytic agent, in the treatment of adult parapneumonic effusions and empyema. Cochrane Database Syst Rev. 2019. https://doi.org/10.1002/14651858.CD002312.pub4.

    Article  PubMed  PubMed Central  Google Scholar 

  23. 23.

    Kheir F, Thakore S, Mehta H, Jantz M, Parikh M, Chee A, et al. Intrapleural Fibrinolytic therapy versus early medical thoracoscopy for treatment of pleural infection: randomized clinical trial. Ann Am Thorac Soc. 2020;17(8):958–64.

    Article  Google Scholar 

  24. 24.

    Mondoni M, Radovanovic D, Sotgiu G, Di Marco F, Carlucci P, Centanni S, Santus P. Interventional pulmonology techniques in elderly patients with comorbidities. Eur J Intern Med. 2019;59:14–22.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

None.

Author information

Affiliations

Authors

Contributions

MM had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. MM and GS wrote the manuscript. LS and GS: performed the data analysis. MM, ST, PC, FG, FG, SC and GS contributed substantially to the study design, data analysis and interpretation. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Michele Mondoni.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

Dr. Michele Mondoni and Prof. Giovanni Sotgiu are senior editorial board members of BMC Pulmonary Medicine.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Table 1 supplement. Microbiological diagnosis of pleural effusion. Table 2 supplement. Chest imaging findings for patients’ classification. Table 3 supplement. Fibrinolysis treatment. Table 4 supplement. Checklist for cohort studies (1), according to the Scottish Intercollegiate Guidelines Network.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Mondoni, M., Saderi, L., Trogu, F. et al. Medical thoracoscopy treatment for pleural infections: a systematic review and meta-analysis. BMC Pulm Med 21, 127 (2021). https://doi.org/10.1186/s12890-021-01492-9

Download citation

Keywords

  • Medical thoracoscopy
  • Pleural infections
  • Empyema
  • Pleuroscopy
  • Parapneumonic effusion
  • Intra-pleural fibrinolysis