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DOI: 10.1055/a-1793-9508
Early prediction of post-ERCP pancreatitis by post-procedure amylase and lipase levels: A systematic review and meta-analysis
Abstract
Background and study aims Post-ERCP pancreatitis (PEP) is the most common complication attributed to the procedure, its incidence being approximately 9.7 %. Numerous studies have evaluated the predictive efficacy of post-procedure serum amylase and lipase levels but with varied procedure-to-test time intervals and cut-off values. The aim of this meta-analysis was to present pooled data from available studies to compare the predictive accuracies of serum amylase and lipase for PEP.
Patients and methods A total of 18 studies were identified after a comprehensive search of various databases until June 2021 that reported the use of pancreatic enzymes for PEP.
Results The sample size consisted of 11,790 ERCPs, of which PEP occurred in 764 (6.48 %). Subgroups for serum lipase and amylase were created based on the cut-off used for diagnosing PEP, and meta-analysis was done for each subgroup. Results showed that serum lipase more than three to four times the upper limit of normal (ULN) performed within 2 to 4 hours of ERCP had the highest pooled sensitivity (92 %) for PEP. Amylase level more than five to six times the ULN was the most specific serum marker with a pooled specificity of 93 %.
Conclusions Our analysis indicates that a lipase level less than three times the ULN within 2 to 4 hours of ERCP can be used as a good predictor to rule out PEP when used as an adjunct to patient clinical presentation. Multicenter randomized controlled trials using lipase and amylase are warranted to further evaluate their PEP predictive accuracy, especially in high-risk patients.
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Introduction
Endoscopic retrograde cholangiopancreatography (ERCP) use has increased in the United States in recent years, with over 150,000 inpatient ERCP procedures being performed each year [1]. Complications related to the procedure have also increased with time and include post-ERCP pancreatitis (PEP), post-procedural bleeding, infection of the biliary tree (cholangitis, cholecystitis), sepsis, and intestinal perforation [1] [2]. PEP is the most common and serious adverse event attributed to this procedure, resulting in an annual estimated cost of over $200 million in the United States [3]. A meta-analysis of 108 randomized controlled trials (RCTs) comprising 13,296 patients reported a 9.7 % overall global incidence of PEP and 13 % in North America [1] [2] [3] [4]. The same meta-analysis also showed an increased PEP incidence in high-risk patients (14.7 %). The majority of PEP cases were mild, with a mortality rate of 0.7 % [4]. A minority of patients (0.5 %) with PEP develop severe diseases, requiring additional resources and extended hospital stay [4]. Given the burden on patients and clinicians, early recognition and aggressive PEP management are paramount.
Moreover, most ERCP procedures are now being performed in the outpatient setting, a significant change in the last decade [5]. These patients are sometimes kept in the hospital under observation (for less than 24 hours) to monitor for development of ERCP-related complications, especially PEP [5]. As the number of outpatient ERCP procedures continues to grow, the need for guidelines related to safe patient discharge and hospitalization becomes magnified. Early measurements of lipase/amylase have been proposed to be convenient indicators of PEP; they may be of high diagnostic value and can guide management decisions if used timely and appropriately, especially in patients with atypical symptoms. Studies have described use of amylase and lipase levels within 2 to 6 hours of ERCP to predict PEP [6]. However, reliable evidence about the standard time to the test and acceptable elevation levels is lacking [6]. In addition, it is well known that there can be a transient increase in pancreatic enzyme levels in up to 75 % of patients after ERCP that may be clinically insignificant, especially in asymptomatic patients [7]. This systematic review and meta-analysis aimed to determine the threshold value of 2 to 4 hours post-procedure serum amylase and lipase levels in predicting PEP. The objective was to analyze the appropriate threshold level of pancreatic enzyme elevation to predict/exclude PEP.
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Methods
Search strategy and study selection
This systematic review and meta-analysis was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) 2009 guidelines [8]. We searched PUBMED/MEDLINE, EMBASE, and Google Scholar databases (inception to June 4, 2021) using keywords and/or Medical Subject Headings (MeSH) for ERCP, pancreatic enzymes, lipase, and amylase. Duplicate studies identified in all databases were deleted manually. In addition, two authors independently reviewed the references and selected studies for full-text screening.
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Inclusion and exclusion criteria
Studies were included if they met the following preset inclusion criteria: 1) articles with patients enrolled for diagnostic and/or therapeutic ERCP; 2) pancreatic enzyme measurement within 2 to 6 hours of the procedure; 3) studies with data on the sensitivity and specificity of post-procedure early amylase/lipase in predicting PEP; 4) studies containing enough information required to build a 2 × 2 contingency table; and 5) published articles in English (abstracts, preprints excluded). Small case series of under 50 patients, review articles, animal models, and any articles where amylase and/or lipase were not studied as the primary objective to diagnose PEP were excluded.
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Data extraction and quality assessment
We extracted data regarding study design, patient characteristics, procedure details, reported outcomes, and limitations ([Table 1]). Two authors (SG and SAAS) independently screened all records identified through database research. A third author (HG) addressed differences in opinion that arose from the same. Each eligible study was thoroughly reviewed to extract the following information: study author, time period, country/region, sample size, enzymes and hours after the ERCP procedure they were measured, the definition used for diagnosing PEP, preventive measures used before the procedure, if any, and data for the 2 × 2 contingency table for each studied test (true positives, false positives, false negatives, and true negatives). Six subgroups were made according to the data available for various enzyme thresholds for both lipase (Groups 1 and 2) and amylase (Groups 3 to 6) ([Table 2]). The Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) tool was used to assess the quality of diagnostic accuracy of studies included in this meta-analysis [9].
Study |
Design |
Total patients |
Patient characteristics |
Procedure (ERCP) characteristics |
Outcomes/results |
Limitations |
Artifon [11]
|
Retrospective single institution |
300 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Gottlieb [12] 1996 |
Prospective single institution |
231 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Hayashi [13]
|
Retrospective single institution |
1403 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Inatomi [14]
|
Prospective multicenter observational study |
1789 |
Age (n = 350) |
Setting
|
Amylase
|
1. CT findings used for diagnosis of PEP. No consensus criteria used |
Ito [15]
|
Prospective single institution |
1291 |
Age
|
Setting
|
Amylase
|
1. Single institution study |
Kapetanos [16]
|
Prospective single institution |
97 PEP 11 (11 %) |
Age
|
Setting
|
Amylase
|
1. Single institution |
Lee [17]
|
Retrospective single institution cohort |
516 |
Mean age
|
Setting
|
Amylase
|
1. Single institution |
Lv [18]
|
Single institution retrospective cohort study between January 2011 and November 2016 |
206 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Martin [19]
|
Retrospective review of clinical trial patient data |
510 |
Age (all)
|
Setting
|
Amylase
|
1. Retrospective design, secondary analysis of a randomized trial |
Minakari [20]
|
Prospective single institution cross-sectional study |
300 |
Mean age
|
Setting
|
Amylase
|
1. Single institution |
Nishino [21]
|
Retrospective single center cohort |
1631 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Papachristos [22]
|
Retrospective single institution analysis |
506 |
Age (all)
|
Setting
|
Amylase
|
1. Single institution |
Sutton [23]
|
Retrospective single institution analysis |
886 |
Mean age
|
Setting
|
Amylase
|
1. Single institution |
Tadehara [24]
|
Retrospective single tertiary university (2 hospitals) |
804 |
Mean age (all)
|
Setting
|
Amylase
|
1. Single institution |
Testoni [25]
|
Prospective design |
409 |
Mean age (all)
|
Setting
|
Amylase
|
1. Small study |
Thomas [26]
|
Prospective design |
263 |
Median age
|
Setting
|
Amylase
|
1. Single institution |
Tseng [27]
|
Prospective design, single institution |
150 |
Age
|
Setting
|
Amylase
|
1. Single institution |
Zhang [28]
|
Retrospective |
Total |
Mean age
|
Setting
|
Amylase
|
1. Retrospective design |
PD, pancreatic duct; ERCP, endoscopy retrograde cholangiopancreatography; PEP, post-ERCP pancreatitis; SOD, sphincter of Oddi dysfunction; NPV, negative predictive value; PPV, postive predictive value; ULN, upper limit of normal; CT, computed tomography; PLR, positive likelihood ratio; NLR, negative likelihood ratio.
ERCP, endoscopic retrograde cholangiopancreatography; ULN, upper limit of normal; PLR, positive likelihood ratio; NLR, negative likelihood ratio; DOR, diagnostic odds ratio; SROC, summary receiver operating characteristic.
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Data analysis
Review Manager 5.4 software (Cochrane Collaboration, Oxford, England) was used to obtain figures of methodological quality. Meta-Disc 1.4 software was used to construct forest plots for pooled sensitivity, specificity, Positive and Negative Likelihood Ratio, Diagnostic Odds Ratio, and Summary receiver operating characteristics (SROC) curves for each subgroup [10]. Random- effects model was employed for pooled analysis because of the presence of significant heterogeneity among the studies. Heterogeneity was assessed using the Cochran Q test and I2 statistics. Sources of heterogeneity for each subgroup were detected using meta-regression analysis; sensitivity analysis was also performed by omitting each included study one by one. Deeks’ funnel plots were used for the detection of any publication bias.
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Results
Literature search
An initial electronic search of all databases yielded a total of 2420 studies. After the removal of duplicates, 241 studies were screened. Of these, 179 were excluded, and full texts of 62 articles were reviewed that ultimately led to 18 studies that met the inclusion criteria [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] (Supplemental Fig. 1). Reference screening of the 18 included studies did not generate any additional studies for review.
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Characteristics of included studies
The study characteristics are summarized in [Table 1]. The included studies yielded a sample size of 11,790 patients that underwent ERCP, of which 764 (6.5 %) developed PEP. All studies except one [14] were performed at a single center. Seven studies were prospective [14] [15] [16] [20] [25] [26] [27] while 11 were retrospective [11] [12] [13] [17] [18] [19] [20] [21] [22] [23] [24] [28] in design. Ten studies were from Asia [13] [14] [15] [17] [18] [20] [21] [24] [27] [28], three each from Europe [9] [16] [25] and Australia [22] [23] [26] and two from the United States [11] [12]. Six studies reported the setting of ERCPs [11] [13] [14] [15] [16] [23] [25] [26] with one being 100 % inpatient [21], two being 100 % outpatient [12] [13], two being mixed [11] [19] and one mostly outpatient [23] (exact incidence not given). Indications of ERCP were reported by 12 studies [11] [13] [14] [15] [16] [17] [18] [19] [22] [23] [26] [27], with choledocholithiasis being the most common indication followed by malignancy.
Ten studies evaluated the diagnostic efficacy of both lipase and amylase [12] [17] [18] [19] [20] [21] [22] [24] [27] [28], whereas eight reported results for amylase only [11] [13] [14] [15] [16] [23] [25] [26]. Lipase and amylase measurements were done within 2 to 4 hours of ERCP in all studies. Eleven studies [11] [12] [13] [18] [19] [20] [22] [23] [26] [27] [28] used established Cotton criteria or Banks (Original or Revised Atlanta) criteria for PEP diagnosis [29] [30] [31], while seven studies used other criteria that ranged from abdominal pain with high amylase to CT-scan findings of pancreatic inflammation only without mention of clinical symptoms [14] [15] [16] [17] [21] [24] [25] ([Table 1]). Four studies reported PEP rates of over 10 % [14] [16] [18] [20], and two of these did not use established PEP diagnosis criteria [14] [16]. Only experienced operators performed ERCPs in two studies, and these two reported the lowest rates of PEP (3.6 % and 3.1 %) [15] [17].
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Predictive value of early measurement of serum lipase for detecting PEP (Groups 1, 2)
Six studies reported the diagnostic value of lipase three to four times the ULN [12] [17] [20] [22] [27] [28] and eight studies reported values of five to six times the ULN [17] [18] [19] [21] [22] [24] [27] [28] done 2 to 4 hours after ERCP. The pooled sensitivity and specificity of lipase level three to four times the ULN was 92 % and 81 %, respectively ([Fig. 1]), with a positive likelihood ratio (PLR) of 4.98 and negative likelihood ratio (NLR) of 0.13 (Supplemental Fig. 2 and Supplemental Fig. 3) with a diagnostic odds ratio (DOR) of 41.19 ([Fig. 1c]). On the other hand, lipase level five to six times the ULN had a lower pooled sensitivity of 87 %, higher pooled specificity of 85 %, higher PLR 6.43, and lower NLR 0.17 with lower DOR of 39.13 ([Fig. 2] and Supplemental Fig. 2 and Supplemental Fig. 3), compared to the lipase three to four times ULN. Overall, serum lipase three to four times ULN performed 2 to 4 hours after ERCP had the highest pooled sensitivity (92 %) of all six enzyme groups for detecting PEP ([Table 2]).
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Predictive value of early measurement of serum amylase for detecting PEP (Groups 3 to 6)
All 18 studies reported diagnostic value of amylase for recognizing PEP 2 to 4 hours after the procedure. Nine studies reported amylase one to one and a half times the ULN (Group 3) [11] [15] [17] [18] [22] [23] [24] [26] [28], nine reported amylase levels two to two and a half times the ULN (Group 4) [12] [13] [14] [17] [19] [20] [23] [26] [28], eight studies reported amylase elevations three to four times the ULN (Group 5) [15] [16] [17] [18] [21] [22] [26] [27] and six studies reported amylase five to six times the ULN (Group 6) [15] [16] [21] [22] [23] [25]. High amylase levels up to one and a half times ULN had the highest pooled sensitivity for the detection of PEP ([Fig. 3]). Serum amylase levels five to six times the ULN had the highest pooled specificity of 93 % ([Fig. 4] ) and highest PLR of 9.97, which was highest in all six groups (including lipase). Groups 4 and 5 (amylase between 2–2.5 and 3–4 times the ULN) (Supplemental Fig. 4a and Supplemental Fig. 5a) had lower sensitivity and specificity than other groups. Based on this, an elevated amylase level of five to six times the ULN seemed the most reliable test to rule-in a diagnosis of PEP, 2 to 4 hours after ERCP ([Table 2]).
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Quality of included studies
The methodological qualities of included studies as assessed using QUADAS-2 are shown in Supplemental Fig. 6. Most studies, including the retrospective design, attempted to decrease recruitment bias by having consecutive patients and clearly identified index and reference tests. However, no study was randomized or blinded. The overall quality of studies was considered moderate.
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Sources of hyeterogeneity
Significant heterogeneity was explored with meta-regression for all the six subgroups; type of study (multicenter vs. single center) and the time of enzyme measurement post-ERCP were found to be the sources in the amylase two to two and a half (Group 4) and lipase five to six subgroup (Group 2), respectively (Supplemental Fig. 7). The use of prophylactic measures before the ERCP procedure was not a significant contributor to heterogeneity, nor was the use of different criteria for the diagnosis of PEP. Sensitivity analysis was also attempted for individual groups, and four studies were found to be contributing to high I2 statistics [12] [14] [21] [26].
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Publications bias
The Deeks’ funnel plots were applied in order to evaluate the existence of publication bias. Significant asymmetry (P < 0.1) was noted in the funnel plot of only one of the six subgroups (Group 2, Lipase five to six times the ULN), indicating no significant publication bias in the studies we included in the meta-analysis (Supplemental Fig. 8).
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Discussion
PEP remains the most common complication of ERCP. Several mechanisms for PEP have been proposed, including thermal injury due to electrosurgical current during biliary or pancreatic sphincterotomy, mechanical injury from instrumentation of papilla and pancreatic duct, enzymatic injury subsequent to intraluminal activation of proteolytic enzymes, hydrostatic injury following injection of contrast medium into the pancreatic duct during sphincter manometry, chemical/allergic injury after injection of contrast medium into the pancreatic duct and infection from the contaminated endoscope and/or accessories [32]. The frequency of PEP depends on patient factors, endoscopist experience, and procedure-related factors. History of previous PEP, female gender, younger age, recurrent pancreatitis, sphincter of Oddi dysfunction are some of the factors used to stratify the patients at high risk of PEP clinically. Procedure-related factors include difficult and/or repeated cannulation, endoscopic sphincterotomy, precut sphincterotomy, and pancreatic duct injection/instrumentation [33]. Rectal administration of indomethacin has proven beneficial in preventing PEP [34], and Protease inhibitors have shown promising results in some clinical trials as well [35]. However, PEP can still occur despite careful patient selection and the use of prevention strategies.
The originally proposed criteria of PEP have been used since 1991, which includes new-onset upper abdominal pain, serum amylase/lipase levels more than three times the ULN, and requirement of 2 to 3 days of inpatient hospitalization [29]. The severity of PEP has been more recently classified with the use of revised Atlanta criteria for the severity of acute pancreatitis [30]. Despite availability, the adoption of these criteria is variable, as evidenced by varied use in the studies included in our review ([Table 1]). In addition, there is no consensus on the levels of serum amylase or lipase levels to rule out PEP.
To the best of our knowledge, this is the first meta-analysis to pool the results of all available individual studies with diverse cut-offs for both serum amylase and lipase levels performed 2 to 4 hours post-ERCP to arrive at a reasonable cut-off value to guide clinicians in early recognition of PEP. Measurement of lipase and amylase levels is an easy, quick, and useful tool to stratify patients who may be at a high risk of developing this complication. Early identification of low-risk patients based on enzyme levels would guide safe discharge of patients undergoing ERCP in the outpatient setting and aid in detecting PEP early in all settings to plan timely management. Both would ultimately help decrease healthcare utilization and costs.
Our study shows serum lipase with a cut-off more than five to six times ULN is the most accurate enzyme to establish a diagnosis of PEP, considering the sensitivity is closest to the specificity with an area under SROC being close to one. However, lipase levels above three to four times ULN had the highest sensitivity, indicating the best diagnostic power to select patients for same-day discharge, while amylase level five to six times the ULN had the highest specificity indicating the most accurate level to select patients needing monitoring and continued hospitalization. Lipase levels more than three to four times the ULN also had the lowest NLR (0.13). Hence, patients with a lipase level less than three times the ULN measured 2 to 4 hours post-procedure may be safely discharged after an outpatient ERCP.
Our study has some limitations. First, the included studies differed in terms of sample size, study design (prospective vs. retrospective), inclusion and exclusion criteria. Secondly, the included studies are far apart in their year of inception, ranging from 1996 [12] to 2020 [18] [28]. Third, the standard definition used for diagnosing PEP was not uniform across studies, nor was the time of measurement of lipase and amylase (ranged between 2 to 6 hours post-ERCP). Finally, some studies used pre-ERCP prophylaxis measures. In contrast, others did not specify its usage that may have impacted results. However, the heterogeneity analysis did not find this bias. Despite these shortcomings, the results of our study provide data to formulate a simple algorithm that could guide management decisions and predict PEP in a timely fashion to minimize morbidity and mortality and save costs associated with unnecessary routine hospitalization for post-ERPC observation. However, future multicenter studies are warranted in this direction as the number of ERCP continues to rise, especially in the outpatient setting. Thus, our study may also provide strong evidence to design such a multicenter randomized trial.
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Conclusions
Serum lipase more than three times ULN measured within 2 to 4 hours of the ERCP provides a reliable estimate of prediction of PEP in symptomatic patients. These results may be used in routine clinical practice to stratify high-risk patients for prompt decisions of either discharge or close observation in the outpatient/inpatient settings, especially in the context of proper clinical presentation.
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Competing interests
Hemant Goyal: Aimloxy LLC. Sonali Sachdeva, Syed Ali Amir Sherazi, Shweta Gupta, Abhilash Perisetto, Aman Ali, Saurabh Chandan declare that they have no conflict of interest.
* These authors contributed equally.
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Corresponding author
Publication History
Received: 29 September 2021
Accepted after revision: 13 January 2022
Article published online:
15 July 2022
© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Kroner PT, Bilal M, Samuel R. et al. Use of ERCP in the United States over the past decade. Endosc Int Open 2020; 8: E761-E769
- 2 Johnson KD, Perisetti A, Tharian B. et al. Endoscopic retrograde cholangiopancreatography-related complications and their management strategies: A “Scoping” literature review. Dig Dis Sci 2020; 65: 361-375
- 3 Elmunzer BJ. Reducing the risk of post-endoscopic retrograde cholangiopancreatography pancreatitis. Dig Endosc 2017; 29: 749-757
- 4 Kochar B, Akshintala VS, Afghani E. et al. Incidence, severity and mortality of post-ERCP pancreatitis: a systematic review by using randomized, controlled trials. Gastrointest Endosc 2015; 81: 143-149.e9
- 5 Kozarek RA. The future of ERCP. Endosc Int Open 2017; 5: E272-E274
- 6 Tryliskyy Y, Bryce GJ. Post-ERCP pancreatitis: Pathophysiology, early identification and risk stratification. Adv Clin Exp Med 2018; 27: 149-154
- 7 Chandrasekhara V, Khashab MA, Muthusamy VR. et al. Adverse events associated with ERCP. Gastrointest Endosc 2017; 85: 32-47
- 8 Moher D, Liberati A, Tetzlaff J. PRISMA Group. et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 2009; 6: e1000097
- 9 Whiting PF, Rutjes AWS, Westwood ME. et al. QUADAS-2: A revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med 2011; 155: 529-536
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