Abstract
Purpose of review
Small-bore chest tubes are widely used in the management of common pleural disease. Guidelines suggest that patients with malignant pleural effusions, pneumothorax and pleural infection may be successfully managed with small-bore drains. However, good quality data is often lacking. This article reviews the evidence for the treatment efficacy and potential adverse effects of different chest tube sizes.
Recent findings
In a large randomised study, the small difference in pain scores between large and small drains was not clinically significant. However, small-bore chest tubes commonly suffer from blockage or inadvertent removal, and may not be as effective in providing successful pleurodesis for malignant pleural effusions.
Summary
Although they may be effective in managing pleural infection, and less painful than large drains, small bore drains may be less effective for pleurodesis.
Keywords: Chest drain, Small bore, Size, Pleural, Effusion, Pneumothorax, Pleural Infection
Introduction
The optimal size of chest tube for management of pleural diseases is not known. Management of malignant pleural effusions traditionally relies on chest tube insertion, drainage of fluid and subsequent talc pleurodesis. The British Thoracic Society (BTS) guidelines [1] advocates the use of smaller tubes (<16 French [F]). The evidence for smaller tubes is based upon case series [1] and three comparative studies [2–4], of which only one small study was randomised [4].
Patients who are symptomatic with a large spontaneous pneumothorax often require chest tube insertion, after attempted aspiration in primary spontaneous pneumothorax. Guidelines suggest that, in clinically stable patients, small-bore (≤14 F) chest drains are sufficient [1, 5]. The management of pleural infection requires drainage of the infected fluid. Traditionally, larger bore chest tubes have been used to drain pus or viscid fluid. However, small-bore chest drains are often the first line of choice of radiologists and respiratory physicians and may be sufficient in many cases. This article will review the evidence for the treatment efficacy and potential adverse effects of different chest tube sizes for these indications.
Efficacy
Pleurodesis for Malignant Pleural Effusion
The most commonly used agent for pleurodesis to prevent fluid recurrence in malignant pleural effusions in the USA and Europe is sterile graded talc. At present, standard practice for talc pleurodesis involves instillation of talc slurry via chest tube (once the pleural fluid has been drained). Success rates for talc pleurodesis are quoted in the BTS guidelines as between 60 and 90% [1]. The same guidelines advocate the use of small-bore chest tubes. However, 7 of the 15 studies cited in the guidelines used large-bore (20–28 F) chest tubes as was historically often used [1]. The evidence for efficacy in small-bore tubes comes from case series, two retrospective comparative studies [2, 3] and only one small randomised study of 18 patients which was a feasibility study, not designed to compare efficacy [4].
The recently published TIME1 (1st Therapeutic Interventions in Malignant Effusion) randomised controlled trial (RCT) assessed the effect of chest tube size and analgesia (NSAIDs vs opiates) on pain and clinical efficacy related to pleurodesis in patients with malignant pleural effusion [6••]. Designed as a non-inferiority study (with a margin of 15%), the authors found that 12 F chest tubes were associated with higher pleurodesis failure rate than 24 F tubes (30 vs 24%), thereby failing to meet non-inferiority criteria (difference, −6%; one-sided 95%CI, −20% to ∞; p = 0.14). However, a large number (206) of the patients recruited in the study had undergone a thoracoscopy (in which a large-bore drain is always placed) and so could not be included in the primary comparison for pleurodesis efficacy by drain size. Nevertheless, the 100 patients included in this analysis still represent the largest study to address this question, from which we cannot conclude equivalence between small- and large-bore drains.
An alternative approach to talc pleurodesis is the poudrage (or insufflation) of talc powder at thoracoscopy. A Cochrane review (2004) found that talc poudrage at thoracoscopy to have an improved relative risk or non-recurrence (1.19) compared to talc slurry [7]. However, a later RCT suggested only a trend towards superiority of talc poudrage and only in a sub-group analysis (excluding those patients with trapped lung) did the authors find a statistically significant difference [8]. Another large non-randomised prospective study found fewer pleurodesis failures in the talc poudrage group. As a result of these conflicting data, an RCT to directly compare talc poudrage to talc slurry for pleurodesis efficacy is currently recruiting in the UK [9]. Although designed to directly compare poudrage vs slurry, this ongoing study may be hampered in its conclusions by the result of the TIME1 study [6••] as the patients in the post-thoracoscopy arm will have large-bore chest drains and those receiving slurry small-bore drains, which may not be as effective as per the TIME1 result.
Pneumothorax
Patients who are symptomatic with large spontaneous pneumothorax often require chest tube insertion. The BTS and the Belgian Society of Pneumology Guidelines suggest attempted needle aspiration first, followed by chest drain if the lung has failed to sufficiently reinflate [1, 10]. The American College of Chest Physicians (ACCP) guidelines advise initial treatment with chest tube, although these may now be out of date (2001) [5]. All guidelines suggest that in clinically stable patients, small-bore (≤14 F) chest drain are sufficient [1, 5, 10]. There exists no randomised trial data. The majority of the evidence for these guidelines comes from multiple case series [11]. One small retrospective comparative study found no difference in treatment success between large-bore (20 F) and small-bore (9 F) chest drain [12].
Failure of treatment of spontaneous pneumothorax is typically defined as the need for further procedure (i.e., another chest tube) or surgical intervention, if the lung fails to re-expand or there is persistent air leak. Suction delivered via high-volume low-pressure system can be employed in such patients. Some physicians may also advocate replacing a small-bore tube with a large-bore one to allow a greater total flow rate of air—as flow rate is proportional to the fifth power of the radius of the tube (Fanning equation). The theory in both cases is that the air can be removed from the pleural cavity at a rate exceeding the egress of air through the breach in the visceral pleura, thereby reinflating the lung. This theory would seem rational if there is clear evidence of insufficient drainage of air (i.e., subcutaneous emphysema, increasing pneumothorax size, or worsening clinical condition). However, there is no good trial evidence to support the use of larger drains or suction in stable patients with a continuing air leak. The idea that the “healing” of the visceral air leak may be promoted by apposition of the visceral and parietal pleural layers has not been proven.
A large-bore chest tube (>28 F) is often recommended in the management of traumatic pneumothorax given the potential need of air and/or blood evacuation. However, this is based upon expert opinion [13] and a recent small RCT, in fact, found that for simple, uncomplicated traumatic pneumothorax, use of a small chest tube (14 F) was associated with reduced pain at insertion and no other clinically important differences (such as drain duration or success rate) [14•].
Pleural Infection
Pleural infection carries a high mortality and 15% large proportion of patients will require surgical intervention [15]. Effective management of pleural infection requires drainage of the infected fluid. Traditionally, larger bore chest tubes have been used to drain pus or viscid fluid. However, numerous case series have reported successful treatment with small-bore chest drains which are often the first line choice of radiologists and respiratory physicians. A largest prospective RCT of pleural infection included 405 patients treated with a range of chest tube sizes [15]. Patients were randomised to intra-pleural fibrinolytics or placebo, rather than small (≤14 F) or larger chest tube, but clinical outcomes, pain, and adverse events could be analysed by chest tube size [16]. The authors found no significant difference in the frequency with which patients either died or required thoracic surgery between groups with chest tubes of varying sizes (<10 F, number dying or needing surgery 21/58 (36%); size 10–14 F, 75/208 (36%); size 15–20 F, 28/70 (40%); size >20 F, 30/69 (44%); p = 0.27). It was concluded that smaller chest tubes could be as effective as large bore and may therefore be the initial treatment of choice for pleural infection. A subsequent randomised study of pleural infection found improved fluid drainage and reduced the frequency of surgical referral in the patients receiving tissue plasminogen activator and DNase (compared to placebo). The majority of these patients were managed with small-bore drains (<15 F) [17].
Adverse Events
The complication rate for chest drain insertion is regularly retrospectively collected as part of the BTS Pleural Procedures Audit. The 2015 audit included 1394 episodes of chest drain insertion, the majority of which (88%) were small bore (<16 F) [18•]. Complications were categorised as immediate or delayed. Immediate complications were failure to place the drain in the pleural space (2.0%), haemothorax (iatrogenic) 1.3%, pain (8%), hypotension (1.9%) and organ puncture (0.6%). Delayed complications were pain (15.6%), drain falling out (9.2%), drain blockage (8.2%), subcutaneous emphysema (4.2%), pleural infection (0.4%), skin infection (1%), re-expansion pulmonary oedema (0.6%) and death (0.1%). A retrospective review of 100 consecutive patients who underwent small-bore chest tube placement found that complications occur less frequently if the drain is placed by expert operators or under radiological/ultrasonographic guidance [19]. Use of ultrasound in chest drain insertion of pleural fluid is now mandatory, but only 70% of chest drains and pleural aspirations were performed using ultrasound guidance in the recent BTS audit [18•].
Pain
Two randomised studies have suggested that large-bore chest tubes may be associated with greater pain. The first was a small (18 patients) feasibility study in patients undergoing tetracycline pleurodesis [4]. The second was a larger (100 patients) study of patients post-thoracic surgery which compared “small” (19 F) drains with standard larger drains (28–32 F) [20].
Analysis of the pain scores in 128 patients in the MIST1 study of pleural infection also found that large bore tubes caused more pain, which was statistically and clinically significant. During chest tube insertion and while the tube was in place, 22/41 (54%) of patients with large bore tube (≥15 F) described moderate/severe pain, compared with only 21/77 (27%) of patients treated with small tube (<15 F) (p = 0.005) [16]. The authors conclude that “27% of patients with larger-size tubes experienced moderate to severe pain that might have been avoided by use of small-size-tubes”.
The larger TIME1 study was undertaken to directly assess pain as a co-primary outcome by chest tube size and analgesia type for malignant effusions [6••]. Data from 300 patients found a statistically significant difference in pain scores between smaller and larger tubes. However, this, on average, was small (6 mm) and was below the published minimum clinically significant threshold for a 100 mm VAS pain score (13 mm; 95%CI, 10–16 mm) [21]. This difference was consistent even when accounting for rescue analgesia usage. Therefore, there would appear to be relatively little clinical benefit in terms of less pain from the use of smaller chest tubes for malignant pleural effusion pleurodesis.
Complications Post-insertion
Small-bore chest tubes appear to be at greater risk of blockage, kinking, or inadvertent removal. Older data suggested a blockage rate of small-bore tubes of 8.1% compared to 5.2% for large-bore tubes in a prospective (non-randomised) study [22]. Recent data suggests a non-significant increase in rate of complications during tube insertion in the small (12 F) group compared to 24 F group (25 vs 14%, p = 0.20) and a higher rate of unintentional displacement of the tube (42 vs 28%) [6••]. Analysis of chest tubes used to treat found a trend towards an increased rate of unplanned chest tube displacement in the smaller tubes (<10 F, 19%; 10–14 F, 23%; size 15–20 F, 0%; >20 F, 17%), but this did not reach statistical significance (p = 0.18) [16]. The complication rates in data collected prospectively in RCTs are higher than those reported in the retrospective BTS audit.
Conclusion
Guidelines suggest that patients with pneumothorax requiring chest tube insertion should be managed with small (rather than large) bore tubes. However, there is a dearth of evidence to support this. Non-RCT data suggests that pleural infection may be successfully initially managed with small bore drains. However, it is now unclear whether small bore chest tubes are as effective as larger drains for pleurodesis for malignant effusions. Large-bore tubes are often regarded being more painful, but recent RCT data now suggested that the small difference in pain scores are not clinical significant in patients with malignant effusion.
Complications in small-bore chest tubes (blockage or inadvertent removal) are higher than larger tubes, and may account for some of the reduced rate of successful pleurodesis. This may be an inherent disadvantage of smaller tubes. Use of small-bore chest tubes in the management of common pleural disease is ubiquitous [18•]. Discerning physicians will need to decide whether to alter their practice with regards to the optimal chest tube size for pleurodesis success.
Compliance with ethical standards
Conflict of interest
Rob Hallifax is funded by a Clinical Training Fellowship from the Medical Research Council (MR/L017091/1) during the course of the study, but declares no other conflicting interest. Ioannis Psallidas is the recipient of a REPSIRE2 European Respiratory Society Fellowship RESPIRE2 – 2015 – 7160, during the course of the study. Nahib Rahman is funded by the Oxford NIHR Biomedical Research Centre.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Licence for Publication
The Corresponding Author has the right to grant on behalf of all authors and does grant on behalf of all authors, a worldwide licence to the Publishers and its licensees in perpetuity, in all forms, formats and media (whether known now or created in the future), to (i) publish, reproduce, distribute, display and store the Contribution; (ii) translate the Contribution into other languages, create adaptations, reprints, include within collections and create summaries, extracts and/or, abstracts of the Contribution; (iii) create any other derivative work(s) based on the Contribution; (iv) to exploit all subsidiary rights in the Contribution; (v) the inclusion of electronic links from the Contribution to third party material wherever it may be located and (vi) licence any third party to do any or all of the above.
Contributorship Statement
All authors included on a paper fulfil the criteria of authorship. The corresponding author (RJ Hallifax) is the guarantor.
Footnotes
This article is part of the Topical Collection on Pleural Diseases and Mesothelioma
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
- 1.Roberts ME, Neville E, Berrisford RG, Antunes G, Ali NJ, BTS Pleural Disease Guideline Group Management of a malignant pleural effusion: British thoracic society pleural disease guideline 2010. Thorax. 2010;65:ii32–40. doi: 10.1136/thx.2010.136994. [DOI] [PubMed] [Google Scholar]
- 2.Parulekar W, Di Primio G, Matzinger F, Dennie C, Bociek G. Use of small-bore vs large-bore chest tubes for treatment of malignant pleural effusions. Chest. 2001;120:19–25. doi: 10.1378/chest.120.1.19. [DOI] [PubMed] [Google Scholar]
- 3.Parker LA, Charnock GC, Delany DJ. Small bore catheter drainage and sclerotherapy for malignant pleural effusions. Cancer. 1989;64:1218–21. doi: 10.1002/1097-0142(19890915)64:6<1218::AID-CNCR2820640609>3.0.CO;2-V. [DOI] [PubMed] [Google Scholar]
- 4.Clementsen P, Evald T, Grode G, Hansen M, Krag Jacobsen G, Faurschou P. Treatment of malignant pleural effusion: pleurodesis using a small percutaneous catheter. A prospective randomized study. Respir Med. 1998;92:593–6. doi: 10.1016/S0954-6111(98)90315-8. [DOI] [PubMed] [Google Scholar]
- 5.Baumann MH, AACP Pneumothorax Consensus Group et al. Management of spontaneous pneumothorax: an American college of chest physicians Delphi consensus statement. Chest. 2001;119:590–602. doi: 10.1378/chest.119.2.590. [DOI] [PubMed] [Google Scholar]
- 6.Rahman NM, Pepperell J, Rehal S, Saba T, Tang A, Ali N, et al. Effect of opioids vs NSAIDs and larger vs smaller chest tube size on pain control and pleurodesis efficacy among patients with malignant pleural effusion: the TIME1 randomized clinical trial. JAMA. 2015;314:2641–53. doi: 10.1001/jama.2015.16840. [DOI] [PubMed] [Google Scholar]
- 7.Shaw P, Agarwal R. Pleurodesis for malignant pleural effusions. Cochrane Database Syst Rev. 2004; CD002916. [DOI] [PubMed]
- 8.Dresler CM, Olak J, Herndon JE, Richards WG, Scalzetti E, Fleishman SB, et al. Phase III intergroup study of talc poudrage vs talc slurry sclerosis for malignant pleural effusion. Chest. 2005;127:909–15. doi: 10.1378/chest.127.3.909. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Bhatnagar R, Laskawiec-Szkonter M, Piotrowska HE, Kahan BC, Hooper CE, Davies HE, et al. Evaluating the efficacy of thoracoscopy and talc poudrage versus pleurodesis using talc slurry (TAPPS trial): protocol of an open-label randomised controlled trial. BMJ Open. 2014;4 doi: 10.1136/bmjopen-2014-007045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.De Leyn P, Lismonde M, Ninane V, et al. Guidelines belgian society of pneumology. Guidelines on the management of spontaneous pneumothorax. Acta Chir Belg. 2005;105:265–7. doi: 10.1080/00015458.2005.11679714. [DOI] [PubMed] [Google Scholar]
- 11.MacDuff A, Arnold A, Harvey J. Management of spontaneous pneumothorax: British Thoracic Society pleural disease guideline 2010. Thorax. 2010;65:ii18–31. doi: 10.1136/thx.2010.136986. [DOI] [PubMed] [Google Scholar]
- 12.Vedam H, Barnes DJ. Comparison of large- and small-bore intercostal catheters in the management of spontaneous pneumothorax. Intern Med J. 2003;33:495–9. doi: 10.1046/j.1445-5994.2003.00467.x. [DOI] [PubMed] [Google Scholar]
- 13.Baumann MH. Pleural disease: an international textbook. London: Arnold Publishers; 2003. [Google Scholar]
- 14.Kulvatunyou N, Erickson L, Vijayasekaran A, Gries L, Joseph B, Friese RF, et al. Randomized clinical trial of pigtail catheter versus chest tube in injured patients with uncomplicated traumatic pneumothorax. Br J Surg. 2014;101:17–22. doi: 10.1002/bjs.9377. [DOI] [PubMed] [Google Scholar]
- 15.Maskell NA, Nunn A, Davies RJ. Intrapleural streptokinase for pleural infection. BMJ. 2006;332:552. doi: 10.1136/bmj.332.7540.552. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Rahman NM, Maskell NA, Davies CW, Hedley EL, Nunn AJ, Gleeson FV, et al. The relationship between chest tube size and clinical outcome in pleural infection. Chest. 2010;137:536–43. doi: 10.1378/chest.09-1044. [DOI] [PubMed] [Google Scholar]
- 17.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. doi: 10.1056/NEJMoa1012740. [DOI] [PubMed] [Google Scholar]
- 18.• Hooper CE, Welham SA, Maskell NA, British Thoracic Society. Pleural procedures and patient safety: a national BTS audit of practice. Thorax. 2015;70:189–91. Recent British Thoracic Society audit of chest drain usage includes data on 1394 patients. [DOI] [PubMed]
- 19.Davies HE, Merchant S, McGown A. A study of the complications of small bore ‘Seldinger’ intercostal chest drains. Respirology. 2008;13:603–7. doi: 10.1111/j.1440-1843.2008.01296.x. [DOI] [PubMed] [Google Scholar]
- 20.Terzi A, Feil B, Bonadiman C, Lonardoni A, Spilimbergo I, Pergher S, et al. The use of flexible spiral drains after non-cardiac thoracic surgery. A clinical study. Eur J Cardiothorac Surg. 2005;27:34–7. doi: 10.1016/j.ejcts.2004.10.016. [DOI] [PubMed] [Google Scholar]
- 21.Gallagher EJ, Liebman M, Bijur PE. Prospective validation of clinically important changes in pain severity measured on a visual analog scale. Ann Emerg Med. 2001;38:633–8. doi: 10.1067/mem.2001.118863. [DOI] [PubMed] [Google Scholar]
- 22.Collop NA, Kim S, Sahn SA. Analysis of tube thoracostomy performed by pulmonologists at a teaching hospital. Chest. 1997;112:709–13. doi: 10.1378/chest.112.3.709. [DOI] [PubMed] [Google Scholar]