Background and objectives The global incidence of hospitalisation due to acute pancreatitis (AP) has been rising in the recent decades. In the USA alone, there was a 13.2% increase between 2009 and 2012 compared with 2002–2005. There remains a lack of approved treatments to prevent disease progression, leaving many liable to developing complications that include multisystem organ failure (OF) and death. This therapeutic deficit raises questions about the scale of the current burden of illness (BOI) associated with severe forms of AP. The aim of the systematic literature review (SLR) was to assess clinical, humanistic, and economic outcomes associated with moderately severe AP (MSAP) and severe AP (SAP) in the USA and the European Union-5 (EU-5).
Methods Systematic searches were conducted in MEDLINE and Embase to identify studies published in English (between 2007 and 2017) that reported on the BOI of MSAP and/or SAP. Manual searches of ‘grey’ literature sources were also conducted.
Results The SLR identified 19 studies which indicated that 15%–20% of patients with AP progress to more severe forms of the disease, up to 10.5% of those with SAP require surgery for complications, and up to 40% die during hospitalisation. By contrast, there appears to be a lack of data on the extent to which SAP affects patients’ quality of life.
Conclusion The available evidence clearly demonstrates that the current management for MSAP and SAP in the USA and EU-5 does not adequately meet patients’ needs. Early identification and intervention for AP is crucial, given the evidence of high rates of morbidity and an associated economic burden that is considerable. Since many patients with the condition present to hospitals at a point when multisystem OF or death is highly likely, there is a particularly urgent need for effective treatment options to prevent disease progression.
- burden of illness
- severe acute pancreatitis
- moderate severe acute pancreatitis
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Acute pancreatitis (AP) involves acute inflammation of the pancreas and, sometimes, adjacent tissues. The occurrence of the condition has been increasing during the last 40 years, with incidence rates ranging from 20 to 80 per 100 000 per annum and varying across countries.1 The proportion of Japan’s population, for example, diagnosed in 2011 was estimated at 49.4 per 100 000, representing a 1.8-fold increase over the previous decade.2 A lower incidence estimate of AP hospital admissions has been reported in Europe. In Scotland, the incidence of AP hospital admissions was estimated at 33.1 per 100 000 per year between 2009 and 2012.3 This, coupled with the rising global epidemiological burden of AP, helps to account for why the condition is a major consumer of healthcare resources and a significant driver of costs. AP accounted for 275 000 hospital admissions and US$2.6 billion in direct treatment costs in 2009 in the USA, where it is one of the leading gastrointestinal diseases.4
AP can rapidly progress into moderately severe AP (MSAP) or severe AP (SAP),5 and there is a lack of standard care of treatment for AP or SAP.6 Therefore, early clinical recognition of AP is crucial to managing disease progression—evidence shows that after the initial 48–72 hours, the progression of disease may be fully established, leading to multisystem organ failure (OF). Historically, however, inconsistencies in defining and categorising the severity of AP have presented a challenge in this regard and have complicated the delivery of appropriate care to patients with this potentially life-threatening condition. Against this background, the revised Atlanta classification (RAC) of AP was proposed in 20125 to address confusion and related variation in classifying AP severity. The RAC defined and classified populations into the following three groups, with persistent OF being the main determinant of severity: mild AP (when no OF or local or systemic complications are present); MSAP (when OF is present and resolves within 48 hours and/or local or systemic complications are present but without persistent OF) and SAP (when OF persists over 48 hours). This classification considers a biphasic natural course of AP, specifically, an early phase in which the presence or absence of persistent OF is determined, and a late phase in which local or systemic complications are investigated.
While the RAC has facilitated recognition of AP and early prediction of its progression to severe forms of the disease, there remain key questions about how patients with, or at risk of, SAP are best managed. Current traditional treatment for SAP, however, has been primarily conservative with more active management of disease progression being limited by the lack of globally recognised treatments. Protease inhibitors, such as gabexate mesilate, nafamostat mesilate and ulinastatin (UTI), have been recommended as treatments for AP and/or SAP in China, Japan and India7–11 but not in other countries. For example, randomised controlled trial (RCT) evidence showed that UTI was associated with a lower risk of mortality among patients with SAP compared with placebo,12–14 but not among patients with AP that was not classified as severe. No product has received such formal approval for SAP in the USA and Europe. Instead, the focus has remained mainly on the management of any known underlying conditions and the provision of supportive care (such as intravenous fluid, antibiotics, drainage therapy and enteral feeding).
The increasing incidence of AP, the potentially devastating consequences of its progression and the lack of licensed pharmacological interventions collectively raise questions about the scale of the current burden among those with the most severe disease. With such issues in mind, we conducted a systematic literature review (SLR) that aimed to provide a broad overview of the burden of illness (BOI) associated with MSAP and SAP in the USA and the European Union-5 (EU-5). A key objective of this research was to systematically collate and present relevant evidence to provide insights into the clinical challenges and outcomes specific to the most severe forms of AP.
The SLR aimed to develop an overview of the BOI associated with MSAP and SAP by creating a framework based on the following review questions:
What are the characteristics of patients diagnosed with MSAP and SAP, in terms of age, gender, aetiologies and comorbidities?
What are the incidence and prevalence of MSAP and SAP? What proportion of patients with AP presentation progresses to MSAP or SAP?
What are the clinical outcomes including mortality, morbidity and complications associated with MSAP and SAP?
What is the quality of life (QoL) of patients diagnosed with MSAP or SAP?
What is the economic burden of MSAP and SAP?
What real-world interventions are being given to patients with MSAP and SAP in the context of the lack of approved specific treatments for AP, MSAP or SAP?
The SLR followed a prespecified review protocol (online supplementary appendix A) and was conducted in accordance with the quality standards recommended by the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) statement15 and the Cochrane Handbook for Systematic Reviews.16
Searches were conducted in MEDLINE (including MEDLINE In-Process) and Embase. Only studies that met all inclusion criteria were included. MSAP was defined as a separate AP severity entity beginning in 20125; consequently, separate searches for AP and SAP were conducted to maximise the chances of identifying relevant data on MSAP and SAP and to address the heterogeneity in how these two disease groups have been defined in the recent literature.
The separate search strategies included a combination of controlled vocabulary and free-text terms, as recommended by the Cochrane Collaboration.17 Full details of the searches are described in the online supplementary appendix A. Additionally, proceedings from the previous 3 years (2015–2017) of key conferences were also manually searched. Bibliographies of all relevant SLRs identified during the evidence search were also reviewed to identify any relevant missing publications.
Studies selection and data extraction
A three-stage screening process was applied to determine the most relevant studies as defined by the protocol. First, title and abstract screening of all unique references identified in both literature databases and grey sources was reviewed against these selection criteria. Studies that reported on multiple outcomes were cross-checked to ensure that all relevant data sources on a particular outcome were considered for inclusion.
Second, owing to the high volume of evidence retrieved, additional selection criteria were applied systematically. For AP and MSAP studies, only those published after 2012 (the year of publication of the RAC) were ultimately included. For the SAP studies, those published between 2007 and 2017 were considered for inclusion.
Finally, the full-text versions of all the publications considered relevant based on the additional criteria were assessed for their suitability for inclusion and full data extraction. All publications were reviewed by one researcher and 50% of the screening decisions were validated by a second, senior researcher. Any discrepancies were resolved by a third researcher.
Relevant data were fully extracted by one investigator using a predesigned template separated by outcome. All data was validated by a second investigator and any discrepancies were resolved by a third investigator.
Synthesis of results
During data extraction and evidence synthesis, it was noted that there was marked variation in how AP severity had been classified across included studies. This inconsistency mainly reflected differences in the time of data collection, as well as the introduction of different classification systems. Accordingly, to enable cross-study comparison and accurate presentation of outcomes by severity group, the populations included in the studies were reclassified as part of the review using the RAC 2012 criteria, where possible. If the authors had not provided such data, their definitions of various forms of AP were accepted as reported. When a study presented data for more than one severity group, these subgroup results were presented separately in the SLR for MSAP and SAP. Studies providing data on mixed-severity populations without stratification of results by severity were not included in the synthesis of results.
The AP and SAP searches (electronic and conference proceedings) yielded a total of 4925 unique records, of which 1024 full-text publications were reviewed. A total of 118 unique studies presenting information on the outcomes of interest for all AP severity groups across the two searches were included (figure 1). After the reclassification of populations using the RAC 2012 criteria, 19 studies (reported in 21 publications) that included MSAP and/or SAP patient populations were identified and further considered in this SLR (figures 1 and 2). Of note, 52 of the 118 studies exclusively included patients with mild AP and 47 included mixed AP severity; those were not considered further in this SLR with the exception of one study with mixed AP severity3 which provided information on the size of the SAP population subgroup. This study3 was included in the reporting of epidemiological outcomes.
Six18–24 (reported in seven publications) of the 19 included studies were US based. Of the 13 EU-5 studies, five3 25–28 were conducted in the UK, three each in Germany29–31 and Italy,32–34 and one each in France35 and Spain.36 Overall, most studies were of a retrospective design (13 studies),3 21–23 25–33 were based on single-centre hospitals (13)18–22 24–26 28 29 31 33 35 36 and were principally tertiary referral units for which the reporting was exclusively on patients with SAP (10).22 23 25–31 33 The sample size of these studies varied considerably, from 2025 (in a single-centre UK study) to 2677 (for a study based on the UK national intensive care unit (ICU) database).27 Four studies19 21 24 36 (reported in five publications) presented subgroup information for patients with MSAP and these are presented separately.
Characteristics, aetiology and comorbidities of patients with MSAP and SAP
Most of the patients with MSAP and SAP in the included studies were men (51%–71.4%)21 33 and all were aged in their 50s (52.5–65.8)22 32 (tables 1 and 2). Gallstone/biliary disease and alcohol were the most common aetiological factors in both the USA and EU-5 studies. Most specifically, among the SAP studies, gallstone/biliary aetiology was present in 31%29–45%19 of patients in the USA and 33%24–61.1%34 of those in the EU-5 studies, whereas alcohol aetiology was present in 17%22–33%24 of patients in the USA and 8.4%34 in the EU-5. Although, idiopathic aetiology was not widely reported in the included studies, it still accounted for up to 20%24 (USA) and 13.6%36 (EU-5) of SAP cases. A similar trend in idiopathic aetiology was identified in the studies including patients with MSAP.19 21 24 36
Given the variations in diagnosis and severity assessment criteria of AP across studies over previous decades, the rapidly evolving features of disease progression, and the fact that most studies of patients with SAP were conducted in single-centre specialist hospitals, it is difficult to derive definitive data on key aspects of the epidemiology of MSAP or SAP, particularly in the USA.
In our review, only one EU-5 study3 reported on the incidence of patients with SAP who required critical care admission (data collected between 2009–2012 and found this to be 5.9/100 000 per year (table 3). Another study from Italy reported that the proportion of AP patients progressing into SAP to be 14.2%.34
Overall, mortality and morbidity increased with disease severity across the studies (tables 4 and 5). Results from four studies19 21 24 36 presenting within-study comparisons of outcomes by AP severity group provide more reliable estimates of differences using a relatively homogeneous population (in terms of the study setting, years of data collection, AP severity classification systems) compared with cross-study comparisons. In three of these studies, the risk of death for patients with MSAP was 0%19 24 36 compared with 21%–40%19 ,24 for patients with SAP. A similar pattern regarding SAP mortality was found across the other 14 studies,18 22 23 25–35 with the risk ranging from 13.6%27 to 41.9%27; EU-5 estimates on mortality were higher for SAP than US estimates (41.9%).27 However, the available EU-5 estimates on SAP mortality need to be viewed with caution because of the lack of reported information to allow reclassification of patients according to the RAC 2012 criteria.
The longer term mortality for patients with SAP (4 years postdischarge) was 12.3% as reported by one study.32
Morbidity and complications
A total of 15 studies (11 from the EU-5 and four from the USA) reported outcomes relating to morbidity or complications associated with either MSAP (four studies)19 21 24 36 or SAP (13 studies)18–20 24 25 27 29–36 (table 4). Reported high morbidity across studies included severe systemic inflammatory response syndrome (SIRS; estimated to occur in 65% of US patients with SAP19; no data reported for patients with SAP in the EU-5), multisystem OF (US studies: 47.4%–60%18 19; EU-5 studies: generally 25%–36.4%,31 36 with one small study (n=35)35 reporting a significantly lower occurrence of 4.2% among patients with SAP) and admission to critical care (US studies: 80%–93%, EU-5 studies: 60.7%).19 24 35 Limited evidence was found for the proportion of patients with SAP with infected pancreatic necrosis (IPN; 21.1%–32%)18 19 in the USA or those needing surgery due to pancreatic necrosis (PN; 4.8%–10.5%)27 34 in the EU-5.
Although the morbidity of MSAP was not found to be as high as in patients with SAP, limited evidence (mainly from US studies) showed that the condition was often still associated with poor outcomes. For instance, 48%19 had SIRS, 26.1%21 had OF and up to 23%21 were admitted to the ICU. Similarly, since some studies did not provide sufficient information to allow reclassification of patients according to RAC 2012, estimates from the EU-5 studies should be interpreted with caution.
Limited evidence was identified on the humanistic burden of SAP from one US retrospective study22 and no studies reporting on such outcomes were identified for MSAP. The US retrospective study22 included surviving patients with SAP who required ICU admission (at a median of 42 months follow-up) and showed that QoL (as measured by the 36-item Short Form survey) appeared to be acceptable compared with that of their healthy peers.
Twenty-three studies (12 from the USA and 11 from the EU-5)19 22 24–27 29 30 33 36–48 reporting on economic outcomes related to SAP and MSAP were identified in this review. One study in patients with SAP reported the mean inpatient costs of US$136 730 per patient (cost year not reported (NR)) for those who were transferred to the ICU and did not survive, compared with US$88 434 for those who did survive.22
In the USA, patients with MSAP stayed in the hospital for a range of 624–1219 days; this duration was much shorter than for those with SAP (16.5–40 days).22 This wide span for the SAP group reflects differences in severity classification and the type of complications involved. More specifically, patients with longer hospital stays were those with the most severe forms of disease. This included patients with peri-PN or PN, IPN (15–21 days in hospital)38 45 compared with those without these complications: (4 days)44; multisystem OF (19–30 days),42 compared with those without (7–9 days)); isolated renal or pulmonary failure (24.7 and 28.8 days, respectively)37 and those requiring admission to the ICU (38–40 days).22
In general, studies from the USA evaluating ICU length of stay (LOS) reported similar results: 2.5–4 days19 24 for MSAP and 4.5–14 days19 24 for SAP. The one exception was one a retrospective study involving patients with SAP in which those who survived hospital admission for AP had an ICU LOS of 15 days and those who did not stayed in the ICU for 28 days.22 This reflects the variations in disease severity and the associated number of complications across studies.
There was a similar trend in the length of ICU stay across the EU-5 studies (MSAP: 7.6 days (study not systematically identified)36 and SAP: 3.827–28.4 days; both studies not systematically identified).36 In patients with SAP, most studies reported hospital LOS ranging from 21 to 51 days (all studies not systematically identified).25 29 30 47 48 More specifically, patients with ≥100 mL extrapancreatic necrosis volumes and those rated as severe on the CT severity index had the highest hospital LOS (39.2 and 59.8 days, respectively; study not systematically identified).46 However, a few studies reported shorter LOS in patients who survived admission to the ICU (15 days),27 presurgery patients for IPN (12.6 days)33 and patients admitted to the ICU in a tertiary referral centre (4 days; study not systematically identified).26
Need for interventions for patients with MSAP and SAP
In US studies, the proportion of patients with MSAP given supportive interventions currently available for AP (eg, nutritional support, drainage, mechanical ventilation (MV)) was 3.7224–51%19; however, as expected, the proportion was higher for those with SAP (47%–90%).19 21
The use of supportive interventions in the EU-5 studies followed the same trend as the USA, with patients with SAP being more likely to require different interventions (such as MV, vasoactive support, percutaneous or transgastric drainage or renal replacement therapy (5%–94.7%)26 36 compared with patients with MSAP (0%–16.7%).36 Among patients with SAP, those who required such interventions most frequently were those with PN (89.5%)30 and those who developed complications during admission to the ICU (81.8%–94.7%).36 However, no significant differences were found in surgery rates between studies of patients with SAP (5%–26.7%)25 26 and studies of patients with mixed AP/SAP (data not presented).
To our knowledge, this SLR provides a unique overview of the BOI associated with severe forms of AP, spanning epidemiological, clinical, humanistic and economic outcomes. It surpasses the scope of previous overviews on AP by taking an in-depth look at the BOI associated with MSAP and SAP, as defined by the RAC. In doing so, the results of this SLR not only highlight the high burden associated with SAP and with most outcomes for MSAP but also underline the key differences in the outlook of the two conditions.
Evidence on the clinical and economic consequences of these more severe forms of AP showcases their significant additional burden. Studies including patients with SAP typically reported a much higher proportion of patients experiencing adverse clinical outcomes compared with patients with MSAP, even though there was wide variation in the results primarily due to the heterogeneous patient populations across studies. This also holds true for other outcomes including comorbidities and complications, economic burden and the use of interventions targeting complications or supportive care; these trends were generally similar in the USA and the EU-5.
The data clearly demonstrates that despite recent advances in standardising how severe forms of AP are recognised and classified, many patients progress to SAP, a condition that is often fatal. That this remains common, even in industrialised countries with sophisticated healthcare systems, accentuates how little clinicians can currently offer patients to prevent or effectively manage such disease progression. The lack of such targeted treatment is likely to represent an ever-growing problem given current epidemiology trends towards more common global occurrence of AP.
Strength and limitations
The major strength of this study is the systematic approach of identification and collection of the most relevant evidence to facilitate cross-study comparisons. This was achieved by reclassifying patients based on severity criteria using the most recent international classification tool (RAC 2012). However, because of the variations in diagnosis criteria and severity assessment of AP across studies, some that did not report data on persistent OF (single or multiple, lasting for ≥48 hours) could not be reclassified using the RAC 2012. It is possible there was an under-reporting of the occurrence of SAP or complications related to SAP in those studies. On the other hand, for SAP studies (as defined by the authors) published before 2012, there could be an overestimation of the occurrence of SAP because their categorisation of this condition may have included some patients who would now be classified as having MSAP according to RAC 2012 criteria. The assessment of the extent to which such underestimation or overestimation occurred was beyond the scope of the review.
This study was also limited by scarce data on outcomes for MSAP, which is not surprising given that this severity category was only created in 2012 by the RAC. Further research is needed to determine to what extent some of the aggressive interventions commonly used for patients with SAP (such as surgeries, drainage, renal replacement therapy and catheterisation) are necessary for patients with MSAP which will result to limiting complications related to these interventions and hospital treatment costs.
There is also only limited evidence on key epidemiological features of AP because of the lack of data on the true population prevalence of MSAP and SAP in this study. It is key to identify the proportion of patients who initially appear with a mild form and later progress to more serious forms of disease (MSAP, SAP) to investigate the epidemiology of AP. This is particularly important for identifying the population size for potential targeted preventive interventions, potential transfer to the ICU for specialist treatment and active interventions. Ideally, a prospective-based, multicentre study which follows patients who present with AP symptoms and further develop severe forms of the disease will provide data with more generalisable results for the MSAP and AP population size. However, data in the literature was scarce.
There was insufficient data assessing economic burden—only limited evidence was found on the inpatient costs for patients with SAP who were transferred to the ICU, and no data were found for patients with MSAP. Similarly, the evidence was sparse on the humanistic consequences of SAP, a crucial requirement for understanding the impact of the condition on patients and carers.
Lastly, given the variations across studies in terms of setting, baseline patient characteristics and diagnostic/disease severity criteria, meta-analyses of the results were not possible.
Early and accurate classification of the severity of AP is crucial for managing the disease and preventing its progression. Evidence shows that after the initial 48–72 hours, the progression of AP to SAP may be fully established and multisystem OF may be inevitable. Despite the advances in scoring systems to more accurately recognise AP severity, more than 15%–20% of patients with AP will develop SAP and up to 40% of this subgroup will die as a result. This and other aspects of the BOI associated with SAP, and to a lesser extent, MSAP highlight the limitations of current therapy, particularly the lack of approved interventions that target disease progression.
Colleen Dumont from Evidera also provided writing and editing assistance.
Contributors GS and JP contributed to the study design. GS was responsible for the data analysis. GS and YG contributed to the data collection and drafting of the manuscript. JP was responsible for the study conception. II and JP contributed to the critical revision of the manuscript. All authors contributed to the data interpretation.
Funding Takeda provided the funding for the study and for the manuscript.
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.