Systematic review

Systematic review of pneumothoraces after endoscopic retrograde cholangiopancreatography

DOI: https://doi.org/10.4414/smw.2020.20199
Publication Date: 03.04.2020
Swiss Med Wkly. 2020;150:w20199

Virgilio Lehmannab, Walther Kellerbc, Bernhard Eggera

a Department of Surgery, HFR Fribourg Cantonal Hospital, Fribourg, Switzerland

b Department of Surgery, SZB Biel, Hospital Center Biel, Biel, Switzerland

c Gastroenterological Private Practice, Biel, Switzerland

Summary

AIMS OF THE STUDY

Pneumothoraces after endoscopic retrograde cholangiopancreatography (ERCP) are an uncommon but potentially lethal complication. Little evidence is available on their epidemiology, diagnosis and therapy. We aimed to evaluate current practices and provide recommendations.

METHOD

We systematically reviewed articles from PubMed, Embase, OVID-Medline and the Cochrane Library.

RESULTS

Forty-four publications reported pneumothoraces after ERCP in 49 patients (74% females). Twenty-one patients (43%) had atypical gastrointestinal anatomy, including peri-ampullary diverticula (n = 8), surgical or endoscopic alterations (n = 7), local tumours (n = 3), ulcerations (n = 2) and ectopic papilla (n = 1). Precut (14%) or standard (39%) sphincterotomies were performed. Cannulation was unsuccessful in six ERCPs. Pneumothoraces occurred bilaterally (45%), on the right (37%) or left side (6%), or no side was stated (12%). Nineteen tension pneumothoraces occurred. Perforations were mainly caused by the sphincterotome, peri-ampullary (41%), or the endoscope, distant from the papilla of Vater (23%). Pneumothoraces were sometimes diagnosed only after hospital discharge (14%). Eighteen patients underwent surgical therapy with drainage, repair and/or bypass. Conservative treatment included antibiotics and bowel rest. Most pneumothoraces were drained; 14% resolved without pleural drainage. Overall mortality was 4%. The mean hospital stay was 9.8 days.

CONCLUSIONS

A post-ERCP pneumothorax should be considered when subcutaneous emphysema, cardiovascular instability or respiratory distress occurs. Thoraco-abdominal computed tomography facilitates identification and therapy tailoring. Because of possible late or discrete onset, patients should be monitored carefully.

Keywords: ERCP, cholangiography, endoscopy, papillotomy, sphincterotomy, pneumomediastinum, pneumothorax, pneumoretroperitoneum, pneumoperitoneum, emphysema

Introduction

Since its introduction in 1968 [1], endoscopic retrograde cholangiopancreatography (ERCP) has played a pivotal role in the diagnosis and management of biliary obstructions, in which cases it is routinely performed. Patients are either managed in outpatient settings or require short hospitalisations [2]. However, life-threatening complications can occur, such as pancreatitis (1.30%), cholangitis (0.87%), haemorrhage (0.76%) and perforations (0.58%) [1].

A perforation that develops into a pneumothorax is a rare, but potentially lethal, complication. A previous prospective multicentre study evaluated early major complications after diagnostic and therapeutic ERCPs. That study identified only one pneumothorax out of 111 major complications in 2769 consecutive patients [1]. Scattered evidence and few recommendations are currently available on the diagnosis and management of this complication. We conducted a literature review to evaluate the incidence, diagnosis, and treatment recommendations for these events.

Materials and methods

Article selection

A systematic literature search was conducted in PubMed, Embase, Ovid MEDLINE and the Cochrane Library, with the following search terms in all fields and MeSH terms: “pneumothorax” and “ercp”; “pneumothorax” and “sphincterotomy”; or “pneumothorax” and “papillotomy”. We retrieved all articles published up to 23 September 2018. All available publications were evaluated. Then we screened the references of the selected articles for additional cases, by searching with the terms: “ercp”, “sphincterotomy”, or “papillotomy”; moreover, we applied the secondary search items: “air”, “gas”, “emphysema”, “pneumomediastinum”, “pneumothorax”, “pneumoretroperitoneum”, or “pneumoperitoneum”. The search strategy was validated by our hospital librarian.

All relevant articles were included in the review, according to the criteria of the initial search, including those retrieved from the iterative search through the references.

The reporting of the review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), with the 2009 PRISMA Checklist [3].

Article eligibility

All original articles were eligible, when they reported cases of uni- or bilateral pneumothoraces after an attempted or successful ERCP.

Data extraction

The text and images of the reported cases were screened for air localisation and properties (e.g., side of pneumothorax, subcutaneous emphysema, pneumoperitoneum, pneumoretroperitoneum, pneumomediastinum and tension pneumothorax). The articles were also searched for demographic criteria (age and gender); underlying illness (e.g., biliary stricture, common bile duct stones [CBDS]); atypical anatomy near and distant from the peri-ampullary region (e.g., diverticulum, ulceration, tumour, surgical alterations); procedural steps and success (e.g., a precut papillotomy [PCP], a conventional endoscopic sphincterotomy [ES], cannulation, stent placement, stone extraction); probable cause of the pneumothorax (e.g., gastrointestinal perforations with localisation, endoscopy-independent causes); diagnostic tools utilised (fluoroscopy, transit study, conventional radiography, or computed tomography [CT]); treatment modalities (pleural drainage, antibiotic therapy, bowel rest or surgery); time to presentation of the pneumothorax; and the final outcome (hospital stay and/or reported death).

Definitions

If a PCP was performed, any further mention of an ES was ignored. ERCP was defined as unsuccessful, when a CBD cannulation was not achieved.

The cause of the pneumothorax was defined as the most probable cause mentioned by the original authors. Gastrointestinal perforations were classified, based on elements from the text and images, according to a modified Stapfer classification [4] (table 1), with the localisation prioritised. Type I perforations included all endoscope-linked perforations in the gastrointestinal tract, except for those in the peri-ampullary area (in the direct vicinity of the papilla of Vater), which were classified as type II. Type III perforations included guide-wire-linked bile duct injuries and any air leakage, after a previously placed percutaneous transhepatic cholangiodrainage (PTCD) catheter. Type IV perforations included any perforations that were not documented on endoscopy, with imaging tools, or during surgical revision.

Table 1

Modified Stapfer classification [4].

TypeLocation of perforationTypical cause
IGastrointestinal tract wall (classically, the medial or lateral duodenal wall)Endoscope
IIPeri-ampullary area (in the immediate vicinity of the papilla of Vater)Sphincterotome
IIIBile ductsGuide-wire / Basket
IVNo proven perforation (retroperitoneal air alone)Compressed air

The time to presentation was defined as the time between the ERCP and the first described signs or symptoms of a pneumothorax (e.g., emphysema, dyspnoea, reduced chest sounds, cardiovascular instability). The time to presentation was classified qualitatively, as follows: immediate – onset during or in the first hour after the procedure; early – onset within 6 hours of the procedure; or late – later findings or discovery after the initial hospital discharge.

A tension pneumothorax was defined as cardiovascular instability (simultaneous hypotension and tachycardia); a mediastinal shift detected on imaging studies; or the performance of emergency decompression procedures.

Quality assessment

Owing to the nature of the evidence (individual case reports, retrospective case series, reviews of case reports, retrospective cohorts), we conducted a quality assessment according to the tool proposed by Murad at al. [5] and displayed it in a fashion analogous to that suggested by Higgins et al. for systematic reviews of interventions [6].

Statistical analysis

Categorical variables are expressed as the frequency and percentage. Numerical data are expressed as the mean, median and range. Because of the nature of the review (a collection of individual cases), the limited number of cases and the rarity of this complication in prospective studies, further statistical analyses were not conducted.

Results

Article selection

A total of 164 articles were identified and screened. Only one original publication was found in the Cochrane Library. The PRISMA flow chart of the study selection procedure is shown in figure 1. The vast majority of the 44 included publications were in English [4, 746], 4 were in German [42, 47], Spanish [48] or Czech [49]. No publication was excluded for language reasons.

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Figure 1
Flow chart of article selection, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [3]

The above-mentioned search results included all the cases described in the two included reviews [7, 40]. One record, a congress communication, was excluded since its patient collective was already analysed in another publication [8] included in our review.

Three articles included multiple cases [4, 32, 40]. In total, 49 separate cases were identified (table 2).

Table 2

Characteristics of case studies and reviews.

ReferenceYearPatientPatho.Atypical anatomyProcedureTime to pres.PneumothoraxAir repartitionDrainage
(side)
TherapyOutcome
GenderAge (y)SideTensionCause
[7]Al-Ashaal2011W25CBDS UnCImmediateRTIPrp, Pp, PmROP14
[8]Bartosz2014UUUUPCPUU UUUUU
[47]Brueck2010W39CBDSDivES, StEx, stentImmediateB IVPrp, Pp, Pm, SEOLCons7
[9]Colemont1988W62Stricture ES, stentImmediateR IVPrp, Pm, SEØConsS
[10]Doerr1996W81CBDSDiv ImmediateR IIPp, Pm, SERConsS
[11]Ferrara2009M82CBDS ES, StExImmediateLTIVPrp, Pp, Pm, SELCons9
[12]Fujii2010W73StrictureBiliodigStentImmediateB IIIPrp, Pp, Pm, SEBCons7
[13]García-Cano2016W79CBDS ES, StExEarlyR IIIPrp, Pm, SEØCons7
[14]Garmon2013W23CBDS  ImmediateBTIPrp, Pp, Pm, SEO1OP5
[15]Goddard2016M68StrictureTumourUnCImmediateB IIPrp, Pp, Pm, SEORCons6
[16]Greilich2016WUCBDS ES, stentImmediateB Tracheal tearPm, SEUOP21
[17]Gya1989W63CBDS PCPLateR IIPrp, Pm, SEROPS
[18]Han2008M63CBDSUlcUnCImmediateRTIPpROPS
[19]Hui2001W89CBDSBII+RYLARCP, UnCImmediateRTIII RConsS
[20]Iyilikci2009W24CBDS ES, StExImmediateBTIISEBOP13
[21]Keber2015W63CBDSEndoscopic alt.StExImmediateB IIPrp, Pp, SEBOPS
[22]Keskin2014W56CBDS ES, StExImmediateB IIPrp, Pp, Pm, SEBOP7
[23]Kocaman2009M24Stricture StentImmediateB IIIPrp, Pp, Pm, SEBOP8
[24]Kogure2014UUUSurgical alt.DBEUUTUUUUU
[25]Lagoudianakis2006M55CBDSEctPCP, UnCLateR IIPrp, SEØCons16
[26]Linssen2013W89CBDSDivUnCImmediateL IIPp, Pm, SELConsS
[27]Lopes2009UUURY ImmediateUTIII 1ConsU
[28]Lutchmansingh2013W57Stricture ES, stentImmediateB UPrp, Pm, SEOLConsU
[29]Makni2012W40CBDS ES, StExLateRTIPrp, Pp, Pm, SEROPS
[30]Markogiannakis2007W56CBDS ES, StExImmediateBTIVPrp, Pp, Pm, SEBCons10
[48]Menéndez2012W79CBDS  EarlyB IPrp, Pp, Pm, SEUOPS
[31]Morley1997W80StrictureUlcPCPImmediateRTIPp, SEROPS
[32]Neofytou2013W45CBDS ES, StExImmediateR IIPrp, Pp, Pm, SERCons5
W94CBDS  ImmediateRTValsalva RCons8
[33]Ozgonul2010W62Stricture StentLateBTIIPrp, Pp, Pm, SEBOPS
[34]Plönes2012W67Stricture StentImmediateB IPm, SEO1Cons9
[35]Rappaport2017M65Stricture StentLateB IPrp, PmBOPS
[36]Samies2015W81StrictureDivES, stentImmediateL IVPrp, Pm, SEØConsS
[37]Sampaziotis2010W68CBDS ES, StExImmediateB ValsalvaPrp, Pp, Pm, SEBCons4
[38]Savides1993W79StrictureTumourES, stentImmediateB IPrp, Pm, SEBOP12
[39]Scarlett1994W59Stricture PCPImmediateR IIPrp, PpRCons5
[40]Schepers2012W76CBDSTumourES, StEx, stentImmediateBTIIPrp, Pp, Pm, SEBCons10
M77Stricture PCP, stentImmediateB IIPrp, Pm, SEØCons7
W88CBDSDivESEarlyRTIIPrp, Pm, SERConsS
W58Jaundice PCPImmediateR IIPrp, PmØConsS
[41]Schiavon2010W79CBDSDivES, StExImmediateR IIPm, SEØCons10
[42]Schilling2014M41StrictureBiliodigStentImmediateRTStent migrationUROPS
[43]Seymann2010W78CBDSDivStExImmediateB IIPrp, Pm, SEBConsS
[44]Shen2015W82Stricture ES, stentImmediateBTIIPrp, Pm, SEO1ConsS
[45]Shimatani2009UUURYDBEUU USE1ConsS
[46]Song2009W78CBDS ES, StExLateRTIIPrp, Pp, Pm, SERCons
[4]Stapfer
2000W74U  ImmediateU ISEUOP
M43U  ImmediateUTISEUOP16
[49]Valkovský2014W68CBDSDivStExImmediateB IIPrp, Pm, SEBCons20

Ø = no drainage; † = deceased; I, II, III, IV = type of perforation according to Stapfer; alt. = alteration; B = bilateral; BII = Billroth II operation; Biliodig = biliodigestive anastomosis; CBDS = common bile duct stone(s); Cons = conservative treatment; DBE = Double balloon enteroscopy; Div = peri-ampullary diverticulum; Ect = ectopic papilla; ES = standard endoscopic sphincterotomy; F = female; L = left; LARCP = laparoscopic assisted ERCP; M = male; O1 = only one side; OP = surgical treatment; OR = only right; OL = only left; Outcome = hospital stay (in days), survival in deceased patients or in unreported stay duration; Patho. = underlying pathology; PCP = precut papillotomy; Pm = pneumomediastinum; Pp = pneumoperitoneum; pres. = presentation; Prp = pneumoretroperitoneum; R = right; RY = roux-en-Y operation; S = survived; SE = subcutaneous emphysema; StEx = stone extraction; T = tension; U = unreported; Ulc = ulceration; UnC = unsuccessful cannulation

Quality assessment

The results of the quality assessment analysis are displayed in figure 2. For the assesment of the two included reviews, we only considered the quality of their original cases. By design, all case reports and retrospective studies had a selection bias. Exposure (ERCP) was always ascertained, in retrospective studies the outcome (pneumothoraces) was often insufficiently documented. The causes of pneumothoraces were better documented in case reports; however, other causes were not always actively excluded in Stapfer IV injuries. Reporting quality was mostly sufficient to allow an adequate extraction of data, with the exception of retrospective studies.

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Figure 2
Summary of quality assessment adapted from Murad [5].
A: Does the patient(s) represent(s) the whole experience? Might patients with similar presentation not have been reported?
B: Was the ERCP adequately ascertained? 
C: Was the pneumothorax adequately ascertained?
D: Was a plausible etiology proposed, thoroughly described, or other causes ruled out?
E: Was follow-up long enough for outcomes to occur? (NR for case reports)
F: Is/are the case(s) described with sufficient details to allow research replication or inferences to the medical practice?
DBE = double balloon endoscopy; ES = endoscopic sphincterotomy; NR = not relevant; PCP = precut papillotomy; perf. = perforation; PTx = pneumothorax

Data

Table 3 summarises the characteristics of the included cases. There were 36 female and 9 male patients (the gender of 4 patients was not reported), with a median age of 67 years (range 23–94). Atypical local anatomy was present in 21 cases (43%). Peri-ampullary diverticula, a peri-ampullary tumour, a duodenal ulceration or a pancreatic neoplasia that deformed the duodenum were noted on endoscopy in 16, 4, 4 and 2% of cases, respectively. One additional case presented with an ectopic papilla [25]. Six patients had relevant prior surgery, namely one unspecified surgical modification necessitating a double-balloon enteroscopy [24]; three roux-en-Y gastrojejunal reconstructions [19, 27, 45]; two biliodigestive anastomoses, one performed during a liver transplantation [42] and one performed during the repair of a congenital biliary obstruction [12]. One patient had a modified papilla due to previous ES [21]. The main interventional procedures in the entire patient collective were an ES (39%) and a PCP (14%), as well as stenting (31%) or stone extraction (31%). In 6 patients (12%), the intended common bile duct cannulation was not achieved.

Table 3

Summary of findings.

 n
(N = 49)
% or range
Patient demographicsGenderFemale3674%
Male918%
Unreported48%
Median age, y6723–94
AnatomyNo anomaly reported2858%
Atypical anatomy2142%
 Peri-ampullary diverticula816%
Surgical alterations612%
Peri-ampullary or duodenal tumours36%
Ulcerations24%
Ectopic papilla12%
Endoscopic alteration12%
ProceduresStandard endoscopic sphincterotomy1939%
Precut papillotomy714%
Stent1531%
Stone extraction1531%
Unsuccessful cannulation612%
PneumothoraxBilateral2245%
Right1837%
Left36%
Unreported612%
Tension pneumothorax1939%
Cause of pneumothoraxType I perforation1123%
Type II perforation2041%
Type III perforation510%
Type IV perforation510%
Other48%
Unreported48%
Time to pneumothoraxImmediate (<1 h)3674%
Early (1–6 h)36%
Late (>6 h or after discharge from hospital)714%
Unreported36%
Pleural drainageAll pneumothoraces drained3062%
Unilateral drainage in bilateral pneumothoraces612%
Not drained714%
Unreported612%
Therapy for the perforationSurgical repair1837%
Conservative treatment2959%
Unreported24%
OutcomeMean hospital stay, d9.84–21
Median stay, d8.5 
Death24%

In most cases, the cause of the pneumothorax was a duodenal perforation near (type II = 41%) or distant from the papilla (type I = 23%). The next most frequent cause was the appearance of air in a retroperitoneal location, but without a proven perforation (type IV = 10%). Five type III perforations were found: two were due to guide-wire injuries in gastrointestinal strictures [12, 23]; one was caused by the trapping of a CBDS between the wall and a balloon during dilatation [13]; and two were due to insufflation, with air tracking through a previously inserted PTCD catheter [19, 27]. Of the latter two, one resulted from overpressure in the afferent loop of a roux-en-Y reconstruction, with air consecutively tracking through the drained bile ducts, the liver parenchyma, and, eventually, the pleural space; and the other one was the result of an iatrogenic injury due to a transdiaphragmatic catheter insertion. In one rather peculiar case, a very late onset pneumothorax occurred, owing to a biliary stent dislocation and perforation in an intrathoracic herniated colon, which caused a colothoracic fistula [42]. Finally, three publications reported extra-intestinal causes, including a tracheal perforation [16] and a forced Valsalva manoeuvre [32, 37].

Most reported pneumothoraces (74%) were diagnosed peri-interventionally, as a result of the immediate onset of clinical symptoms; only 6% were diagnosed early after the intervention. In 7 cases (14%) with no or few specific symptoms, the pneumothorax was diagnosed as late as 3 days after the procedure [46]. Moreover, the stent migration was diagnosed at an unclear, but even later time point [42].

Variable diagnostic tools were used to identify the site of perforation, including peri-interventional cholangiography (or fluoroscopy), X-rays, and CT scans. Pneumothoraces were described as bilateral, right-sided or left-sided, in 22, 18, and 3 cases, respectively. In 6 cases, the exact localisation of the pneumothorax was not reported. Nineteen patients (39%) had clinical or radiological signs of tension pneumothoraces. Subcutaneous chest emphysema was present in 78% of cases, and one had extended to the orbital region [9]. Pneumomediastinum, pneumoretroperitoneum, and pneumoperitoneum were present in 69, 65, and 45% of cases, respectively.

Most gastrointestinal injuries (59%) could be managed conservatively, with antibiotics and bowel rest, with or without a nasogastric suction tube. However, patients with type I perforations nearly always required surgery (10/11). The one exception was a patient with an oesophageal tear, which was detected as contrast extravasation on imaging, but it could not be identified during an oesophagoscopy [34]. This patient recovered with antibiotics and nasogastric suction alone.

Surgical repair consisted of a direct suture alone [38], combined with an omental patch [31] or combined with a cholecystectomy and T-tube insertion [7, 18, 48]. In others, pyloric exclusion and gastrojejunostomy [4, 29], tube duodenostomy [4, 20, 33], colostomy and mucous fistula [42] were performed. In another two cases the perforation could not be identified at laparotomy [17, 23]. In one case with a tracheal tear treatment consisted of stent placement and interposition of an intercostal muscle flap [16]. Finally, four publications did not report any details on the surgical intervention [14, 21, 22, 35].

Conservative management without a chest tube was successful in 7 cases of uncomplicated pneumothoraces. All 19 tension pneumothoraces were systematically drained. Only 2 of these 19 patients underwent immediate decompression [14, 44].

The mean hospital stay was 9.8 days (range 4–21). Two patients with perforations died. One refused surgery [46] and the other developed septic shock after a 2-cm lateral duodenal wall perforation was treated with a pyloric exclusion and gastrojejunostomy [4].

Discussion

We found that the current published evidence on post-ERCP pneumothoraces was limited. The present review included more than double the number of pneumothorax cases after ERCP, compared with the previous reviews.

Article screening and data gathering were conducted by two authors. However, this study had some potential limitations, besides the already addressed quality issues of the included articles. First, there might have been a reporting bias due to a reluctance of authors to expose disastrous complications, as suggested previously by Schepers [40]. In addition, there might have been a publication bias, because we found studies only on dramatic cases; recently published cases were almost exclusively about bilateral or tension pneumothoraces. Other biases might have arisen because of the heterogeneous case report descriptions and collected data; this heterogeneity might be partly explained by the different professions of the authors (e.g., gastroenterologists, anaesthesiologists, emergency physicians and even cardiologists). However, despite these limitations, we provided a summary of the current evidence, and we highlighted the practices and some correlations and properties that were not previously discussed.

Intervention-related pneumothoraces are always due to leakage of intraluminal air. Therefore, it seems appropriate to compare our findings with studies that reported ERCP-linked perforations. Women and older patients were predominantly affected by this complication. Savides [38] suggested that age-related thinning of the duodenal wall might be a determining factor. However, age and female gender are also the most predominant factors in patients suffering from gallstone disease. Therefore, intervention-related pneumothoraces are much more related to ERCP performed to treat CBDS and much less directly to these two factors [50]. Although studies have shown that women were more prone to developing post-ERCP pancreatitis, no link has been demonstrated between patient sex and a susceptibility to perforations [51].

Consistently with a previous retrospective case control study [52], we identified several local and interventional risk factors for the occurrence of ERCP-related pneumothorax, including an ES, PCP, dilated common bile duct, a dilatation manoeuvre and atypical anatomy. Other recognised contributing factors include the duration of the procedure and the insufflation time after the injury [53]. Because the insufflation time probably determines the amount of air that will leak through the injury, it might contribute to the development of significant pneumothoraces. As a result of the above-mentioned lack of data in the reviewed cases, corroboration was not possible.

Strategies to avoid ERCP-linked complications were not discussed in the reviewed articles. However, such strategies are nicely described in the literature: for example, a magnetic resonance cholangiopancreatography (MRCP)-first approach might minimise unnecessary diagnostic ERCPs; however, it remains a matter of debate whether this approach might diminish the overall complication rate [54]. Anatomical information gained by an MRCP could, in combination with demographic and clinical factors, provide a partial basis for the anticipation of risky constellations. Intra-interventional bail-out strategies could additionally limit injuries in complicated cannulations. Conducting another ERCP after a few days is often successful and should be considered, particularly in the setting of bleeding or increasing papillary oedema. Alternative strategies might also be considered, such as a PTCD or even a surgical revision. These strategies could at least minimise the intervention time and the need for PCPs [55].

The pathophysiological mechanisms of pneumothorax formation during ERCP have been described in the literature. In summary, there are four possible routes to the mediastinal and pleural spaces: (1) in a retroperitoneal perforation, air can track throughout the continuous fascial planes, up to the thoracic cavity [56]; (2) in a free peritoneal perforation, air can communicate between the abdominal and thoracic cavities through diaphragmatic orifices (peritoneal stomata) in porous diaphragm syndromes [23]; (3) in the absence of a true perforation, air can enter the mucosa at a weak spot (e.g., anastomosis, diverticulum) and track along the perineural and perivascular sheaths [12]; (4) finally, air from a ruptured alveolus (through hyperventilation, the Valsalva manoeuvre, or excess positive pressure during ventilation) can track into the perivascular sheath, which could lead to pulmonary interstitial emphysema, and eventually, cause endoscopy-independent pneumothoraces, also known as the Macklin effect [10].

To the best of our knowledge, the right-sided predominance of pneumothoraces remains unexplained. We postulated that air might follow the path of least resistance. Indeed, the development of left pneumothoraces might be discouraged by the presence of adhesions between the retroperitoneum and the anterior aortic sheath, which might form an anatomic barrier.

The consistent presence of a pneumomediastinum in bilateral pneumothoraces suggested bilateral mediastinal tears caused by a tension pneumomediastinum with air leaking into both pleural cavities. Alternatively, some patients might have a congenital or surgically acquired communication between the two pleural spaces; this is known as “buffalo chest syndrome” [57]. In this condition, bilateral pneumothoraces could occur without a pneumomediastinum [20].

The high prevalence of tension (39%) and bilateral (45%) pneumothoraces among the reviewed cases might be due to the above-mentioned publication bias, because only severe cases were published. Alternatively, high pressure insufflation might be another contributing factor; this pressure could either cause decompression to the second hemithorax or lead to the development of tension.

The clinical signs and diagnosis of an ERCP-related perforation have been described extensively [4, 12, 39, 58]. A thoraco-abdominal CT scan is the diagnostic gold standard for evaluating the problem (fig. 3) [59]. The classical clinical signs of small pneumothoraces, such as diminished breath sounds and tympanic percussion, are frequently overlooked, particularly in patients who are otherwise stable post-ERCP. Subcutaneous emphysema, which was often present in the reported cases (78%), is a highly suspicious sign of an air-containing organ perforation, even without pneumothorax formation. A tension pneumothorax should be suspected when patients exhibit neck vein distention, tracheal deviation, tachycardia, and/or desaturation. Moreover, decompensation signs, such as respiratory distress or circulatory instability, should rouse suspicion of a tension pneumothorax, and after clinical confirmation, it should lead to immediate decompression, without further delay, even for imaging. However, in stable patients suspected of having a perforation with pneumothorax, radiographic evaluation should be performed before drainage, as suggested by the authors of a recent review [60].

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Figure 3
Post-ERCP abdominal computed tomography scan of a 75-year old patient at our institution demonstrating bilateral pneumothoraces (*), pneumomediastinum (°), pneumoperitoneum (arrow), and subcutaneous emphysema (SE). A peri-ampullary diverticulum (Div) is also present. A smaller but significant pneumothorax could have been missed, since the thorax was incompletely scanned.

A simple chest X-ray or sonography [53, 61] may exclude relevant pneumothorax formations. However, in accordance with the newest recommendations from the European Society of Gastrointestinal Endoscopy on iatrogenic endoscopic perforations [59], we strongly recommend an imaging evaluation with a thoraco-abdominal CT scan in such patients. The presence of a duodenal diverticulum, the performance of a PCP or ES and long procedure times should be considered reasons to lower the threshold for additional diagnostic studies after the intervention. In the specific case of intra-interventional suspicion of perforation and the beginning of a tension pneumothorax, the use of fluoroscopy, which is typically available in the ERCP-room, might enable an immediate diagnosis [18, 22, 31, 40]. However, minimum pneumothorax formations might be overlooked, due to the supine positioning. Finally, a loss of image resolution might be an indirect sign of extraluminal air formation. This finding should suggest the need for additional imaging studies, such as CT.

It would be appropriate to tailor therapies for treating perforations and pneumothoraces. A step-by-step approach has been advocated, based on the degree of perforation and the evolution of the patient’s injury [4, 12, 39, 58]. In our review, we found that type I perforations were commonly managed operatively, except for small oesophageal tears that could be detected with CT but not by endoscopy [34]. Types II and III perforations were mainly managed conservatively, which is consistent with literature recommendations. However, the time and specifications of antibiotic therapy and bowel rest have not been standardised.

Early treatments for pneumothoraces include supplemental oxygen, close monitoring and iterated evaluations of drainage procedures. Drainage should be evaluated according to the amount of collapsed pulmonary tissue and patient compensation, which also depends on previous lung function. One-sided drainage may be sufficient, even in bilateral pneumothoraces. Therefore, in symmetrical pneumothoraces without instability, decompression and drainage should first be performed on the right side, and then, according to the evolution, a tailored contralateral drainage might be warranted. In any case, pleural drainage might accelerate recovery. In the literature, hospital stays were only reported for four of seven patients who did not receive drainage. As mentioned above, a tension pneumothorax requires prompt management.

It is of pivotal importance to monitor the patient after ERCP. A review [2] suggested that patients in good general condition, without additional risk factors, might be eligible for outpatient ERCPs. The authors mentioned that only 10% of all post-ERCP complications that required treatment presented symptoms after 24 hours. The present review demonstrated that late symptom onset occurred in 14% of patients. Therefore, close monitoring for at least 6 hours after the procedure is mandatory, and at our institutions an overnight stay is standard.

None of the patients included in this review died as a direct result of a pneumothorax; in the patients who died, the perforation and related sepsis were ultimately the cause of death. However, a missed pneumothorax could be lethal when left untreated [60], particularly in patients who require intubation for a surgical revision. Therefore, we advocate that pneumothorax formation should be actively excluded in cases of ERCP-linked perforation, before any further action is taken.

In conclusion, pneumothorax is a rare, but significant complication of ERCP, and it might not become evident until days after the procedure. In particular, after unsuccessful attempts to cannulate the common bile duct, it is mandatory to observe the patient closely. Because of the rarity of this complication, it is essential to report new cases frequently to ensure that physicians remain alert to this phenomenon. Additionally, reviews of reported cases might further refine our knowledge of diagnostic and treatment modalities.

Disclosure statement

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors; the authors remain independent of any funding influence and declare no support from any organisation for the submitted work. All authors declare no financial relationships with any organisations that might have an interest in the submitted work in the previous three years and no other relationships or activities that could appear to have influenced the submitted work.

Correspondence

Prof. Bernhard Egger, MD, HFR Fribourg Cantonal Hospital, Department of Surgery, Chemin des Pensionnats 2–6, CH-1708 Fribourg, Bernhard-egger[at]bluewin.ch

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