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BMJ Clinical Evidence logoLink to BMJ Clinical Evidence
. 2011 Jan 17;2011:1505.

Spontaneous pneumothorax

Abel P Wakai 1
PMCID: PMC3275306  PMID: 21477390

Abstract

Introduction

The incidence of spontaneous pneumothorax is 24/100,000 a year in men and 9.9/100,000 a year in women in England and Wales. The major contributing factor is smoking, which increases the likelihood by 22 times in men, and by 8 times in women. While death from spontaneous pneumothorax is rare, rates of recurrence are high, with one study of men in the USA finding a total recurrence rate of 35%.

Methods and outcomes

We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of treatments in people presenting with spontaneous pneumothorax? What are the effects of interventions to prevent recurrence in people with previous spontaneous pneumothorax? We searched: Medline, Embase, The Cochrane Library, and other important databases up to January 2010 (Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).

Results

We found 17 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.

Conclusions

In this systematic review we present information relating to the effectiveness and safety of the following interventions: chest-tube drainage (alone or plus suction), chest tubes (small, standard sizes, one-way valves), needle aspiration, and pleurodesis.

Key Points

Spontaneous pneumothorax is defined as air entering the pleural space without any provoking factor, such as trauma, surgery, or diagnostic intervention.

  • Incidence is 24/100,000 a year in men, and 10/100,000 a year in women in England and Wales, and the major contributing factor is smoking, which increases the likelihood by 22 times in men and by 8 times in women.

  • While death from spontaneous pneumothorax is rare, rates of recurrence are high, with one study of men in the US finding a total recurrence rate of 35%.

Overall, we found insufficient RCT evidence to determine whether any intervention is more effective than no intervention for spontaneous pneumothorax.

Chest-tube drainage seems to be a useful treatment for spontaneous pneumothorax, although RCT evidence is somewhat sparse.

  • Small (8 French gauge) chest tubes are generally easier to insert, and may reduce the risk of subcutaneous emphysema, although successful resolution may be less likely in people with large pneumothoraces (>50% lung volume). We don't know whether there is a difference in duration of drainage with small tubes.

  • The trials investigating the efficacy of adding suction to chest-tube drainage are too small and underpowered to detect a clinically important difference.

  • We don't know whether using one-way valves on a chest tube is more effective than using drainage bottles with underwater seals. There is a suggestion, however, that one-way valves might reduce hospital admission and the need for analgesia.

It seems that needle aspiration might be beneficial in treating people with spontaneous pneumothorax, although it is not clear whether it is more effective than chest-tube drainage.

Pleurodesis seems to be effective in preventing recurrent spontaneous pneumothorax, although there are some adverse effects associated with the intervention.

  • Chemical pleurodesis successfully reduces recurrence of spontaneous pneumothorax, although the injection has been reported to be intensely painful.

  • Thoracoscopic surgery with talc instillation also seems to reduce recurrence of spontaneous pneumothorax, but leads to a modest increase in pain during the first 3 days.

  • Video-assisted thoracoscopic surgery, while less invasive than thoracotomy, may be associated with higher recurrence rates.

  • We found no RCT evidence examining when pleurodesis should be given, although there is general consensus that it is warranted after the second or third episode of spontaneous pneumothorax.

About this condition

Definition

A pneumothorax is air in the pleural space. A spontaneous pneumothorax occurs when there is no provoking factor — such as trauma, surgery, or diagnostic intervention. It implies a leak of air from the lung parenchyma through the visceral pleura into the pleural space, which causes the lung to collapse and results in pain and shortness of breath. This review does not include people with tension pneumothorax.

Incidence/ Prevalence

In a survey in Minnesota, USA, the incidence of spontaneous pneumothorax was 7/100,000 for men and 1/100,000 for women. In England and Wales, the overall rate of people consulting with pneumothorax (in both primary and secondary care combined) is 24/100,000 a year for men and 10/100,000 a year for women. The overall annual incidence of emergency hospital admissions for pneumothorax in England and Wales is 16.7/100,000 for men and 5.8/100,000 for women. Smoking increases the likelihood of spontaneous pneumothorax by 22 times for men and by 8 times for women. The incidence is directly related to the amount smoked.

Aetiology/ Risk factors

Primary spontaneous pneumothorax is thought to result from congenital abnormality of the visceral pleura, and is typically seen in young, otherwise fit people. Secondary spontaneous pneumothorax is caused by underlying lung disease, typically affecting older people with emphysema or pulmonary fibrosis.

Prognosis

Death from spontaneous pneumothorax is rare, with UK mortality of 1.26 per million a year for men and 0.62 per million a year for women. Published recurrence rates vary. One cohort study in Denmark found that, after a first episode of primary spontaneous pneumothorax, 23% of people had a recurrence within 5 years, most of them within 1 year. Recurrence rates had been thought to increase substantially after the first recurrence, but one retrospective case-control study (147 US military personnel) found that 28% of men with a first primary spontaneous pneumothorax had a recurrence; 23% of the 28% had a second recurrence; and 14% of that 23% had a third recurrence, resulting in a total recurrence rate of 35%.

Aims of intervention

To reduce morbidity; to restore normal function as quickly as possible; to prevent recurrence and mortality, with minimum adverse effects.

Outcomes

Successful resolution of spontaneous pneumothorax after a stated period; time to full expansion of the lung; duration of hospital stay; time off work; adverse effects of treatments (complications including pain, surgical emphysema, wound, and pleural space infection); and rate of recurrence.

Methods

Clinical Evidence search and appraisal January 2010. The following databases were used to identify studies for this systematic review: Medline 1966 to January 2010, Embase 1980 to January 2010, and The Cochrane Database of Systematic Reviews 2009, Issue 4 (1966 to date of issue). An additional search within The Cochrane Library was carried out for the Database of Abstracts of Reviews of Effects (DARE) and the Health Technology Assessment (HTA) database. We also searched for retractions of studies included in the review. Abstracts of the studies retrieved from the initial search were assessed by an information specialist. Selected studies were then sent to the contributor for additional assessment, using predetermined criteria to identify relevant studies. Study design criteria for inclusion in this review were: published systematic reviews of RCTs and RCTs in any language. RCTs had to contain 20 or more individuals of whom 80% or more were followed up. Blinded and non-blinded studies were included. There was no minimum length of follow-up required to include studies. We included systematic reviews of RCTs and RCTs where harms of an included intervention were studied applying the same study design criteria for inclusion as we did for benefits. In addition we use a regular surveillance protocol to capture harms alerts from organisations such as the FDA and the MHRA, which are added to the reviews as required. To aid readability of the numerical data in our reviews, we round many percentages to the nearest whole number. Readers should be aware of this when relating percentages to summary statistics such as relative risks (RRs) and odds ratios (ORs). We have performed a GRADE evaluation of the quality of evidence for interventions included in this review (see table). The categorisation of the quality of the evidence (high, moderate, low, or very low) reflects the quality of evidence available for our chosen outcomes in our defined populations of interest. These categorisations are not necessarily a reflection of the overall methodological quality of any individual study, because the Clinical Evidence population and outcome of choice may represent only a small subset of the total outcomes reported, and population included, in any individual trial. For further details of how we perform the GRADE evaluation and the scoring system we use, please see our website (www.clinicalevidence.com).

Table.

GRADE Evaluation of interventions for Spontaneous pneumothorax.

Important outcomes Duration of hospital stay, Recurrence rates, Resolution rates
Studies (Participants) Outcome Comparison Type of evidence Quality Consistency Directness Effect size GRADE Comment
What are the effects of treatments in people presenting with spontaneous pneumothorax?
1 (18) Resolution rates Needle aspiration versus observation 4 −2 0 0 0 Low Quality points deducted for sparse data and incomplete reporting of results
3 (194) Resolution rates Needle aspiration versus chest-tube drainage 4 −2 0 −1 0 Very low Quality points deducted for sparse data and incomplete reporting of results. Directness point deducted for differences in definition of outcome
3 (194) Duration of hospital stay Needle aspiration versus chest-tube drainage 4 −1 0 0 0 Moderate Quality point deducted for sparse data
3 (194) Recurrence rates Needle aspiration versus chest-tube drainage 4 −2 0 0 0 Low Quality points deducted for sparse data and incomplete reporting of results
1 (26) Resolution rates Small- versus standard-sized chest tubes 4 −1 0 0 0 Moderate Quality point deducted for sparse data
1 (30) Resolution rates One-way valves on chest tubes 4 −1 0 0 0 Moderate Quality point deducted for sparse data
1 (30) Duration of hospital stay One-way valves on chest tubes 4 −1 0 0 +1 High Quality point deducted for sparse data. Effect size point added for RR <0.5
1 RCT and one trial (93) Resolution rates Chest-tube drainage plus suction versus chest-tube drainage alone 4 −3 0 −2 0 Very low Quality points deducted for sparse data, incomplete reporting of results, and inclusion of controlled clinical trial. Directness points deducted for not stating suction pressures used, and not stating whether primary or secondary spontaneous pneumothorax
What are the effects of interventions to prevent recurrence in people with previous spontaneous pneumothorax?
2 (325) Recurrence rates Adding chemical pleurodesis to chest-tube drainage versus chest-tube drainage alone 4 −2 0 0 0 Low Quality points deducted for incomplete reporting of results and for open-label RCT
2 (325) Duration of hospital stay Adding chemical pleurodesis to chest-tube drainage versus chest-tube drainage alone 4 −2 0 0 0 Low Quality points deducted for incomplete reporting of results and for open-label RCT
1 (108) Recurrence rates Thoracoscopic surgery with talc instillation versus chest-tube drainage 4 −1 0 0 0 Moderate Quality point deducted for sparse data
1 (108) Duration of hospital stay Thoracoscopic surgery with talc instillation versus chest-tube drainage 4 −2 0 0 0 Low Quality points deducted for sparse data and incomplete reporting of results
3 (210) Recurrence rates Video-assisted thoracoscopic surgery versus thoracotomy 4 −1 0 0 0 Moderate Quality point deducted for incomplete reporting of results
3 (263) Duration of hospital stay Video-assisted thoracoscopic surgery versus thoracotomy 4 −1 −1 0 0 Low Quality point deducted for incomplete reporting of results. Consistency point deducted for conflicting results

We initially allocate 4 points to evidence from RCTs, and 2 points to evidence from observational studies. To attain the final GRADE score for a given comparison, points are deducted or added from this initial score based on preset criteria relating to the categories of quality, directness, consistency, and effect size. Quality: based on issues affecting methodological rigour (e.g., incomplete reporting of results, quasi-randomisation, sparse data [<200 people in the analysis]). Consistency: based on similarity of results across studies. Directness: based on generalisability of population or outcomes. Effect size: based on magnitude of effect as measured by statistics such as relative risk, odds ratio, or hazard ratio.

Glossary

French gauge

A measure of the size of a catheter or drainage tube defined (in France by JFB Charrière in 1842) to be the outside diameter of the tube in units of 1/3 mm. A 12 French gauge tube has an outer diameter of 4 mm. Sometimes the French gauge is called the Charrière (Ch) gauge.

High-quality evidence

Further research is very unlikely to change our confidence in the estimate of effect.

Low-quality evidence

Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.

Moderate-quality evidence

Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.

Very low-quality evidence

Any estimate of effect is very uncertain.

The information contained in this publication is intended for medical professionals. Categories presented in Clinical Evidence indicate a judgement about the strength of the evidence available to our contributors prior to publication and the relevant importance of benefit and harms. We rely on our contributors to confirm the accuracy of the information presented and to adhere to describe accepted practices. Readers should be aware that professionals in the field may have different opinions. Because of this and regular advances in medical research we strongly recommend that readers' independently verify specified treatments and drugs including manufacturers' guidance. Also, the categories do not indicate whether a particular treatment is generally appropriate or whether it is suitable for a particular individual. Ultimately it is the readers' responsibility to make their own professional judgements, so to appropriately advise and treat their patients. To the fullest extent permitted by law, BMJ Publishing Group Limited and its editors are not responsible for any losses, injury or damage caused to any person or property (including under contract, by negligence, products liability or otherwise) whether they be direct or indirect, special, incidental or consequential, resulting from the application of the information in this publication.

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BMJ Clin Evid. 2011 Jan 17;2011:1505.

Needle aspiration

Summary

It seems that needle aspiration might be beneficial in treating people with spontaneous pneumothorax, although it is not clear whether it is more effective than chest-tube drainage.

Benefits and harms

Needle aspiration versus observation:

We found no systematic review. We found one small RCT.

Resolution rates

Compared with observation Needle aspiration may be more effective at increasing resolution rates (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Resolution

RCT
21 people Mean time to full expansion
1.6 weeks in 8 people successfully treated with needle aspiration
3.2 weeks in 10 people treated with conservative treatment

Significance assessment not performed

Duration of hospital stay

No data from the following reference on this outcome.

Recurrence rates

No data from the following reference on this outcome.

Adverse effects

No data from the following reference on this outcome.

Needle aspiration versus chest-tube drainage:

We found two systematic reviews. The first review (search date 2003, 3 RCTs, 194 people with primary or recurrent spontaneous pneumothorax) compared needle aspiration versus chest-tube drainage. The second systematic review (search date 2006) excluded two of the RCTs identified by the first review because it was unclear whether participants in these RCTs were experiencing a first episode of spontaneous pneumothorax. The second review included one RCT (60 people) identified by the first review and found similar results to the first review.

Resolution rates

Compared with chest-tube drainage We don't know whether needle aspiration is more effective at achieving success rates at 1 week in people with spontaneous pneumothorax (very low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Resolution

Systematic review
194 people with primary or recurrent spontaneous pneumothorax
3 RCTs in this analysis
Success at 1 week or more
with needle aspiration
with chest-tube drainage
Absolute results not reported

RR 0.86
95% CI 0.67 to 1.11
Not significant

Duration of hospital stay

Compared with chest-tube drainage Needle aspiration seems more effective at reducing the duration of hospital stay in people with spontaneous pneumothorax (moderate-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Hospital stay

Systematic review
194 people with primary or recurrent spontaneous pneumothorax
3 RCTs in this analysis
Hospital stay
with needle aspiration
with chest-tube drainage
Absolute results not reported

WMD –1.3 days
95% CI –2.2 days to –0.39 days
P = 0.005
Effect size not calculated needle aspiration

Recurrence rates

Compared with chest-tube drainage We don't know whether needle aspiration is more effective at preventing recurrence of spontaneous pneumothorax at 1 year (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Recurrence

Systematic review
194 people with primary or recurrent spontaneous pneumothorax
3 RCTs in this analysis
Recurrence at 1 year
with needle aspiration
with chest-tube drainage
Absolute results not reported

RR 0.73
95% CI 0.39 to 1.38
Not significant

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects

RCT
People with pneumothorax
In review
Mean daily pain scores during their hospital stay
0.7 with needle aspiration
1.5 with chest-tube drainage

P <0.001
Effect size not calculated needle aspiration

RCT
People with pneumothorax
In review
Pain or dyspnoea
with needle aspiration
with chest-tube drainage
Absolute results reported graphically

Reported as not significant
Not significant

Systematic review
60 people
Data from 1 RCT
Proportion of people requiring hospital admission after treatment
14/27 (52%) with needle aspiration
33/33 (100%) with chest-tube drainage

RR 0.52
95% CI 0.36 to 0.75
Small effect size needle aspiration

Further information on studies

The RCT comparing needle aspiration versus observation was published as a letter.

Rates of successful resolution could not be combined by the review because of differences in outcome definitions. Pain and dyspnoea scores could not be combined because of differences in outcome definitions.

The RCT did not assess pain. One of the systematic reviews that identified this RCT stated that it reported no complications in the simple aspiration group, but did not report on complications in the intercostal tube drainage group.

Comment

None.

Substantive changes

No new evidence

BMJ Clin Evid. 2011 Jan 17;2011:1505.

Chest-tube drainage alone

Summary

Chest-tube drainage seems to be a useful treatment for spontaneous pneumothorax, although the evidence is somewhat sparse.

Benefits and harms

Chest-tube drainage versus observation:

We found no systematic review or RCTs.

Chest-tube drainage versus needle aspiration:

See option on needle aspiration.

Chest-tube drainage versus chest-tube drainage plus suction:

See option on chest-tube drainage plus suction.

Further information on studies

None.

Comment

None.

Substantive changes

No new evidence

BMJ Clin Evid. 2011 Jan 17;2011:1505.

Small- versus standard-sized chest tubes for drainage

Summary

Small (8 French gauge) chest tubes are generally easier to insert, and may reduce the risk of subcutaneous emphysema, although successful resolution may be less likely in people with large pneumothoraces (>50% lung volume). We don't know whether there is a difference in duration of drainage with small tubes.

Benefits and harms

Small- versus standard-sized chest tubes:

We found no systematic review. We found no RCTs, but found one small non-randomised trial (44 people), which compared small-gauge catheters (8 French gauge) versus standard-sized chest tubes (see further information on studies).

Resolution rates

Small-sized chest tubes compared with standard-sized chest tubes Small-gauge tubes seem less effective at achieving successful resolution in people with large pneumothoraces (moderate-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Resolution
26 people with large pneumothoraces (>50% lung volume)
Subgroup analysis
Proportion of people with successful resolution
8/14 (57%) with small-gauge catheters (8 French gauge)
12/12 (100%) with standard-sized chest tubes

P <0.05
Effect size not calculated standard-sized chest tubes

Duration of hospital stay

No data from the following reference on this outcome.

Recurrence rates

No data from the following reference on this outcome.

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects
44 people Subcutaneous emphysema
0/21 (0%) with small-gauge catheters (8 French gauge)
9/23 (39%) with standard-sized chest tubes

P <0.05
Effect size not calculated small-gauge catheters

Further information on studies

The RCT found no significant difference in duration of drainage between groups (5 days with small tubes v 6 days with standard chest tubes; reported as not significant, no further data reported).

Comment

Clinical guide:

Small-gauge chest tubes are usually easier to insert.

Substantive changes

No new evidence

BMJ Clin Evid. 2011 Jan 17;2011:1505.

One-way valves on chest tubes

Summary

We don't know whether using one-way valves on a chest tube is more effective than using drainage bottles with underwater seals. There is a suggestion, however, that one-way valves might reduce hospital admission and the need for analgesia.

Benefits and harms

One-way valves on chest tubes:

We found no systematic review. We found one RCT comparing a chest tube (13 French gauge) connected to a one-way valve versus a chest tube (14 French gauge) connected to a drainage bottle with an underwater seal.

Resolution rates

Compared with drainage bottles One-way valves and drainage bottles with underwater seals seem equally effective at improving expansion or nearly complete expansion of the lung at 48 hours in people with spontaneous pneumothorax and respiratory distress (moderate-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Resolution

RCT
30 people with spontaneous pneumothorax and respiratory distress Rate of resolution (complete or nearly complete expansion) 48 hours
15/17 (88%) with chest tube (13 French gauge) connected to a one-way valve
11/13 (85%) with chest tube (14 French gauge) connected to a drainage bottle with an underwater seal

RR 1.04
95% CI 0.78 to 1.39
Not significant

Duration of hospital stay

Compared with drainage bottles One-way valves are more effective at reducing hospital admissions in people with spontaneous pneumothorax and respiratory distress (high-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Hospital stay

RCT
30 people with spontaneous pneumothorax and respiratory distress Hospital admissions
5/17 (29%) with chest tube (13 French gauge) connected to a one-way valve
13/13 (100%) with chest tube (14 French gauge) connected to a drainage bottle with an underwater seal

RR 0.29
95% CI 0.14 to 0.61
Moderate effect size chest tube connected to a one-way valve

Recurrence rates

No data from the following reference on this outcome.

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects

RCT
30 people with spontaneous pneumothorax and respiratory distress Rates of complications (need for a second drain)
3/17 (18%) with chest tube (13 French gauge) connected to a one-way valve
1/13 (8%) with chest tube (14 French gauge) connected to a drainage bottle with an underwater seal

Reported as not significant
Not significant

RCT
30 people with spontaneous pneumothorax and respiratory distress Proportion of people who required analgesia
5/17 (29%) with chest tube (13 French gauge) connected to a one-way valve
10/13 (77%) with chest tube (14 French gauge) connected to a drainage bottle with an underwater seal

RR 0.38
95% CI 0.17 to 0.85
Moderate effect size chest tube connected to a one-way valve

RCT
30 people with spontaneous pneumothorax and respiratory distress Rates of complications (skin emphysema)
3/17 (18%) with chest tube (13 French gauge) connected to a one-way valve
3/13 (23%) with chest tube (14 French gauge) connected to a drainage bottle with an underwater seal

Reported as not significant
Not significant

Further information on studies

None.

Comment

None.

Substantive changes

No new evidence

BMJ Clin Evid. 2011 Jan 17;2011:1505.

Chest-tube drainage plus suction

Summary

The trials investigating the efficacy of adding suction to chest-tube drainage are too small and underpowered to detect a clinically important difference.

Benefits and harms

Chest-tube drainage plus suction versus chest-tube drainage alone:

We found no systematic review, but found one RCT and one controlled clinical trial comparing chest-tube drainage using an underwater seal only versus drainage plus suction.

Resolution rates

Compared with chest-tube drainage alone Chest-tube drainage plus suction may be no more effective at increasing lung expansion at 10 days in people with primary or secondary spontaneous pneumothorax (very low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Resolution

RCT
53 people; 23 with primary and 30 with secondary spontaneous pneumothorax Proportion of people with full lung expansion 10 days
13/23 (57%) with chest-tube drainage plus suction
15/30 (50%) with chest-tube drainage using an underwater seal only

ARI +7%
95% CI –21% to +34%
RR 1.13
95% CI 0.68 to 1.88
The RCT is likely to have been too small to detect a clinically important difference
Not significant

Pseudo-randomised trial
40 people Time taken for lung expansion
5.2 days with chest-tube drainage with low-pressure suction
6.2 days with chest-tube drainage without suction

Reported as not significant
CI not reported
Not significant

Duration of hospital stay

No data from the following reference on this outcome.

Recurrence rates

No data from the following reference on this outcome.

Adverse effects

No data from the following reference on this outcome.

Further information on studies

None.

Comment

None.

Substantive changes

No new evidence

BMJ Clin Evid. 2011 Jan 17;2011:1505.

Pleurodesis

Summary

Pleurodesis seems to be effective in preventing recurrent spontaneous pneumothorax, although there are some adverse effects associated with the intervention. Chemical pleurodesis successfully reduces recurrence of spontaneous pneumothorax, although the injection has been reported to be intensely painful. Thoracoscopic surgery with talc instillation also seems to reduce recurrence of spontaneous pneumothorax, but leads to a modest increase in pain during the first 3 days. Video-assisted thoracoscopic surgery, while less invasive than thoracotomy, may be associated with higher recurrence rates.

Benefits and harms

Adding chemical pleurodesis to chest-tube drainage versus chest-tube drainage alone:

We found no systematic review. We found two RCTs.

Recurrence rates

Adding chemical pleurodesis to chest-tube drainage compared with chest-tube drainage alone We don't know whether chemical pleurodesis using tetracycline or talcum powder is more effective at reducing recurrence rates at 30 months or 4.6 years in people with spontaneous pneumothorax (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Recurrence

RCT
229 men with pneumothorax successfully treated by chest-tube drainage; mean age 54 years; 55% with COPD Recurrence rates over 30 months
26/104 (25%) with adding intrapleural instillation of tetracycline
44/108 (41%) with chest-tube drainage alone

RR 0.61
95% CI 0.41 to 0.92
Small effect size adding intrapleural instillation of tetracycline

RCT
3-armed trial
96 people treated with chest-tube drainage Pneumothorax recurrence rate 4.6 years
2/24 (8%) with talcum powder pleurodesis
9/25 (36%) with no further treatment

Difference between talcum powder pleurodesis and no further treatment reported as significant
Effect size not calculated talcum powder pleurodesis

RCT
3-armed trial
96 people treated with chest-tube drainage Pneumothorax recurrence rate 4.6 years
3/23 (13%) with tetracycline pleurodesis
9/25 (36%) with no further treatment

Difference between tetracycline pleurodesis and no further treatment reported as not significant
Not significant

Duration of hospital stay

Chemical pleurodesis plus chest-tube drainage compared with chest-tube drainage alone Chemical pleurodesis plus chest-tube drainage may be no more effective at reducing the duration of hospital stay in people with spontaneous pneumothorax (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Hospital stay

RCT
229 men with pneumothorax successfully treated by chest-tube drainage; mean age 54 years; 55% with COPD Length of hospital stay
5 days with adding intrapleural instillation of tetracycline
7 days with chest-tube drainage alone

Reported as not significant
Not significant

RCT
3-armed trial
96 people treated with chest-tube drainage Mean hospital stay
7 days with tetracycline pleurodesis
6 days with talcum powder pleurodesis
6 days with chest-tube drainage alone

Reported as not significant
Not significant

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects

RCT
229 men with pneumothorax successfully treated by chest-tube drainage; mean age 54 years; 55% with COPD Adverse effects
with adding intrapleural instillation of tetracycline
with chest-tube drainage alone

RCT
3-armed trial
96 people treated with chest-tube drainage Proportion of people reporting pain
17/33 (52%) with tetracycline pleurodesis
14/29 (48%) with talcum powder pleurodesis
18/34 (53%) with chest-tube drainage alone

Significance assessment not performed

Thoracoscopic surgery with talc instillation versus chest-tube drainage:

We found no systematic review. We found one multicentre RCT that compared thoracoscopic surgery plus talcum powder instillation versus chest-tube drainage.

Recurrence rates

Thoracoscopic surgery with talc instillation compared with chest-tube drainage Thoracoscopic surgery with talc instillation seems more effective at reducing recurrence rates at 5 years in people with primary spontaneous pneumothorax (moderate-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Recurrence

RCT
108 people with large primary spontaneous pneumothorax or primary spontaneous pneumothorax that had failed aspiration Recurrence rate 5 years
3/59 (5%) with thoracoscopic surgery plus talcum powder instillation
16/47 (34%) with chest-tube drainage

P <0.01
Effect size not calculated thoracoscopic surgery plus talcum powder instillation

Duration of hospital stay

Thoracoscopic surgery with talc instillation compared with chest-tube drainage Thoracoscopic surgery with talc instillation may be no more effective at reducing the duration of hospital stay in people with spontaneous pneumothorax (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Hospital stay

RCT
108 people with large primary spontaneous pneumothorax or primary spontaneous pneumothorax that had failed aspiration Mean hospital stay
8.0 days with thoracoscopic surgery plus talcum powder instillation
7.4 days with chest-tube drainage

Significance assessment not performed

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects

RCT
108 people with large primary spontaneous pneumothorax or primary spontaneous pneumothorax that had failed aspiration Pain first 3 days
with thoracoscopic surgery plus talcum powder instillation
with chest-tube drainage
Absolute results reported graphically

Modestly, but significantly, increased with thoracoscopic surgery compared with chest-tube drainage
Effect size not calculated chest-tube drainage

RCT
108 people with large primary spontaneous pneumothorax or primary spontaneous pneumothorax that had failed aspiration
Subgroup analysis
Pain in people receiving systemic opioids
with thoracoscopic surgery plus talcum powder instillation
with chest-tube drainage
Absolute results reported graphically

See further information on studies
Not significant

Video-assisted thoracoscopic surgery versus thoracotomy:

We found one systematic review (search date 2006, 4 RCTs, 353 people) comparing video-assisted thoracoscopic surgery versus open surgery (thoracotomy). The review assessed recurrence rates (see further information on studies) and did not assess other outcomes. Three RCTs identified by the review also assessed other outcomes, and so we have reported these separately. The fourth RCT is awaiting assessment in relation to its coverage of these outcomes.

Recurrence rates

Video-assisted thoracoscopic surgery compared with open surgery (thoracotomy) Video-assisted thoracoscopic surgery may be associated with higher recurrence rates in people with primary or secondary spontaneous pneumothorax, although the difference between groups did not reach significance (moderate-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Recurrence

Systematic review
210 people
3 RCTs in this analysis
Recurrence rates
with video-assisted thoracoscopic surgery
with open surgery (thoracotomy)
Absolute results not reported

RR 3.95
95% CI 0.86 to 18.19
The review reported that recurrence rates were higher in people having video-assisted thoracoscopic surgery
Not significant

Duration of hospital stay

Video-assisted thoracoscopic surgery versus thoracotomy We don't know whether video-assisted thoracoscopic surgery is more effective at reducing the duration of hospital stay in people with primary or secondary spontaneous pneumothorax (low-quality evidence).

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Hospital stay

RCT
60 people with primary spontaneous pneumothorax, either first recurrence or non-resolving first episode
In review
Mean hospital stay
6.5 days with video-assisted surgery
10.7 days with thoracotomy

P <0.0001
Effect size not calculated video-assisted surgery

RCT
60 people; 30 with primary pneumothorax, 30 with secondary, either with recurrence or an air leak persisting for >5 days
In review
Mean hospital stay
4 days with video-assisted thoracoscopic surgery
5 days with thoracotomy

Reported as not significant
May have been underpowered to detect a clinically important difference between groups
Not significant

RCT
143 people
In review
Length of hospital stay
with video-assisted thoracoscopic surgery (47 people)
with thoracotomy (96 people)
Absolute results not reported

Adverse effects

Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Adverse effects

RCT
143 people
In review
Postoperative pain
with video-assisted thoracoscopic surgery (47 people)
with thoracotomy (96 people)
Absolute results not reported

Reported as not significant
Not significant

RCT
60 people with primary spontaneous pneumothorax, either first recurrence or non-resolving first episode
In review
Use of analgesia
with video-assisted surgery
with thoracotomy
Absolute results not reported

Reported significantly reduced with video-assisted surgery
Effect size not calculated video-assisted surgery

RCT
60 people; 30 with primary pneumothorax, 30 with secondary, either with recurrence or an air leak persisting for >5 days
In review
Use of analgesia
with video-assisted thoracoscopic surgery
with thoracotomy
Absolute results not reported

Reported as not significant
The RCT may have been underpowered to detect a clinically important difference between groups
Not significant

Chemical versus surgical pleurodesis:

We found no systematic review or RCTs.

Further information on studies

The RCT found no significant difference between groups in 5-year mortality (40/113 [35%] with adding intrapleural instillation of tetracycline v 42/116 [36%] with chest-tube drainage alone; RR 0.98, 95% CI 0.62 to 1.38).

The RCT did not establish a protocol for analgesia; 4 centres gave postoperative systemic opioids and three did not.

The review's primary objective was to assess consistency between randomised and non-randomised studies assessing recurrence rates. It found coherence in results with different levels of evidence, namely that video-assisted thoracoscopic surgery was associated with higher recurrence rates.

The RCT reported that 3 people with secondary spontaneous pneumothorax died: 1 receiving video-assisted thoracoscopic surgery and 2 receiving thoracotomy, 1 of whom previously had unsuccessful video-assisted thoracoscopic surgery

Comment

None.

Substantive changes

Pleurodesis New evidence added. Categorisation unchanged (Trade-off between benefits and harms).

BMJ Clin Evid. 2011 Jan 17;2011:1505.

Optimal timing of pleurodesis (after first, second, or subsequent episodes)

Summary

There is no evidence examining when pleurodesis should be given, although there is general consensus that it is warranted after the second or third episode of spontaneous pneumothorax.

Benefits and harms

Optimal timing of pleurodesis:

We found no systematic review. We found no RCTs or high-quality cohort studies comparing pleurodesis undertaken at different times (after the first, second, or subsequent episode/s of spontaneous pneumothorax; see comment below).

Further information on studies

None.

Comment

Clinical guide:

One observational study suggested that the 5-year recurrence rate after a first pneumothorax is about 28%, so there may be little reason to perform pleurodesis after the first episode of pneumothorax. There has been consensus that pleurodesis is warranted after the second or third episode of pneumothorax. Even though the probability of success with pleurodesis is high, clinicians will have to weigh the likelihood of recurrence against the morbidity associated with the procedure. Chemical pleurodesis may be appropriate for people unfit or unwilling to have surgery.

Substantive changes

No new evidence


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