Skip to main content
Annals of Saudi Medicine logoLink to Annals of Saudi Medicine
. 2022 Aug 4;42(4):276-287. doi: 10.5144/0256-4947.2022.276

COVID-19 and Acute Pancreatitis: A Systematic Review of Case Reports and Case Series

Vasiliki E Georgakopoulou a,, Aikaterini Gkoufa b, Nikolaos Garmpis c, Sotiria Makrodimitri a, Chrysovalantis V Papageorgiou a, Danai Barlampa d, Anna Garmpi b, Serafeim Chiapoutakis e, Pagona Sklapani f, Nikolaos Trakas g, Christos Damaskos h
PMCID: PMC9357298  PMID: 35933608

Abstract

BACKGROUND:

Coronavirus disease 2019 (COVID-19) presents mainly with mild symptoms and involvement of the respiratory system. Acute pancreatitis has also been reported during the course of COVID-19.

OBJECTIVE:

Our aim is to review and analyze all reported cases of COVID-19 associated acute pancreatitis, reporting the demographics, clinical characteristics, laboratory and imaging findings, comorbidities and outcomes.

DATA SOURCES:

We conducted a systematic search of Pubmed/MEDLINE, SciELO and Google Scholar to identify case reports and case series, reporting COVID-19 associated acute pancreatitis in adults.

STUDY SELECTION:

There were no ethnicity, gender or language restrictions. The following terms were searched in combination:“COVID-19” OR “SARS-CoV-2” OR “Coronavirus 19” AND “Pancreatic Inflammation” OR “Pancreatitis” OR “Pancreatic Injury” OR “Pancreatic Disease” OR “Pancreatic Damage”. Case reports and case series describing COVID-19 associated acute pancreatitis in adults were included. COVID-19 infection was established with testing of nasal and throat swabs using reverse transcription polymerase chain reaction. The diagnosis of acute pancreatitis was confirmed in accordance to the revised criteria of Atlanta classification of the Acute Pancreatitis Classification Working Group. Exclusion of other causes of acute pancreatitis was also required for the selection of the cases.

DATA EXTRACTION:

The following data were extracted from each report: the first author, year of publication, age of the patient, gender, gastrointestinal symptoms due to acute pancreatitis, respiratory-general symptoms, COVID-19 severity, underlying diseases, laboratory findings, imaging features and outcome.

DATA SYNTHESIS:

Finally, we identified and analyzed 31 articles (30 case reports and 1 case series of 2 cases), which included 32 cases of COVID-19 induced acute pancreatitis.

CONCLUSION:

COVID-19 associated acute pancreatitis affected mostly females. The median age of the patients was 53.5 years. Concerning laboratory findings, lipase and amylase were greater than three times the ULN while WBC counts and CRP were elevated in the most of the cases. The most frequent gastrointestinal, respiratory and general symptom was abdominal pain, dyspnea and fever, respectively. The most common imaging feature was acute interstitial edematous pancreatitis and the most frequent comorbidity was arterial hypertension while several patients had no medical history. The outcome was favorable despite the fact that most of the patients experienced severe and critical illness.

LIMITATIONS:

Our results are limited by the quality and extent of the data in the reports. More specifically, case series and case reports are unchecked, and while they can recommend hypotheses they are not able to confirm robust associations.

CONFLICT OF INTEREST:

None

INTRODUCTION

Acute pancreatitis is the leading cause of hospital admission for disorders of the gastrointestinal tract in several countries.1 Gallstones and alcohol overconsumption are well-established risk factors. Other factors, possibly genetic, probably have a role. Drugs are an additional causative factor of acute pancreatitis. Moreover, smoking and diabetes type II increase the probability of acute pancreatitis development.

Mild cases are generally successfully managed with a conservative approach. Severe cases frequently need admission to an intensive care unit for monitoring and managing complications of the disease, which are related to high rates of mortality, even when the treatment is optimal.2

Approximately 10% of cases of acute pancreatitis are considered to have infectious microorganisms as an underlying cause.3 These microorganisms include viruses (like Coxsackie B and hepatitis), bacteria (like Mycoplasma pneumonia and Leptospira), and parasites (like Ascaris lumbricoides and Fasciola hepatica). Each microorganism leads to acute pancreatitis through various mechanisms.3 Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread rapidly worldwide and is characterized by the World Health Organization as an international public health emergency. Besides typical symptoms and signs from respiratory system, acute pancreatitis has been reported during the course of the disease.4

COVID-19 associated pancreatic inflammation results from the expression of angiotensin converting enzyme 2 (ACE2) receptors in pancreatic tissue. The structural protein glycosylated-spike (S) protein, encoded by SARS-CoV-2 genome, primarily induces the immune response of the host. The S protein binds to ACE2 receptor sites on the cell surface membrane mediating the cell invasion. ACE2 receptors are not only expressed in lung alveolar type-2 cells. ACE2 receptors are expressed in the pancreas, in both exocrine glands and islets, in a higher grade than in the lungs.5,6 This expression of ACE2 receptors can lead to pancreatic cell damage during COVID-19 infection. Direct cytotoxic action of SARS-CoV-2 or indirect, immune-mediated, systemic inflammation could be the mechanism of pathogenesis for pancreatic injury.5,6

Globally, the incidence of acute pancreatitis ranges between 5 and 80 per 100 000 population, with the highest incidence observed in the United States and Finland.7 The incidence of SARS-CoV-2 infection varies among regions. Cyprus has the highest incidence of COVID-19 cases among its population in Europe at 55 424 per 100 000 people, followed by a rate of 52 738 per 100 000 in Iceland.8 In United States the incidence ranges between 2698 cases per 100 000 population in Hawaii and 14 541 cases per 100 000 population in North Dakota.8 In this study, we aimed to review and analyze all reported cases of COVID-19 associated acute pancreatitis, reporting the demographics, clinical characteristics, laboratory and imaging findings, comorbidities and outcomes.

CASES AND METHODS

Search strategy and article selection

We conducted a systematic search of Pubmed/MEDLINE, SciELO and Google Scholar to identify case reports and case series, reporting COVID-19 associated acute pancreatitis in adults, using the Patient, Intervention, Comparison and Outcome (PICO) Model.9 There were no ethnicity or gender restrictions. In addition, there were no language restrictions. We assessed all articles published from 01 January 2020 to 20 April 2021. A protocol of the study, including details of the methods used in the systematic review has been deposited in the PROSPERO database (https://www.crd.york.ac.uk/PROSPERO/) with the registration number CRD42021266917.

The following terms were searched in combination:“COVID-19” OR “SARS-CoV-2” OR “Coronavirus 19” AND “Pancreatic Inflammation” OR “Pancreatitis” OR “Pancreatic Injury” OR “Pancreatic Disease” OR “Pancreatic Damage”. The search was conducted by two reviewers (VEG, CD). Articles were first screened for relevance by title. Then they were evaluated by abstract. The relevant case reports were enrolled for full-text review. Moreover, a manual search of the lists of the references of these texts was performed for identifying additional relevant case reports and case series.

Case reports and case series describing COVID-19 associated acute pancreatitis in adults were included. COVID-19 infection was established with testing of nasal and throat swabs using reverse transcription polymerase chain reaction. The diagnosis of acute pancreatitis was confirmed in accordance to the revised criteria of the Atlanta Acute Pancreatitis Classification Working Group.10 At least two of the following three criteria had to be present for a diagnosis of acute pancreatitis: a) typical pain of acute pancreatitis (acute onset of a severe and persistent epigastric pain often with radiation to the back) b) serum lipase or amylase elevated at least three times the upper limit of normal; c) compatible imaging findings of acute pancreatitis on abdominal computed tomography (CT), on magnetic resonance imaging (MRI) or abdominal ultrasonography (U/S).10 Exclusion of other causes of acute pancreatitis was also required for the selection of the cases.

Data extraction

The following data were extracted from each report: the first author, year of publication, age of the patient, gender, gastrointestinal symptoms due to acute pancreatitis, respiratory-general symptoms, COVID-19 severity, underlying diseases, laboratory findings, imaging features and outcome. The tool suggested by Murad et al to assess the methodological quality and synthesis of the case series and case reports was utilized.11 The possible best score was 6 for a case report or a case series of good quality. The patients represented the whole experience of the researchers, the diagnosis of SARS-CoV-2 and the outcomes were adequately ascertained; other causes of pancreatitis were excluded. The follow-up was long enough for outcomes to occur and the described cases had sufficient details to allow other researchers to replicate the findings. Table 1 shows the use of the tool suggested by Murad et al in our review. In addition, we followed the PRISMA (Preferred Reporting Items For Systematic Reviews And Meta-Analyses) guidelines for writing this review.12

Table 1.

Tool for evaluating the methodological quality of case reports and case series of the current review suggested by Murad et al.11

Domains Leading explanatory questions Cases and cases series included in the current review Score
Selection 1. Does the patient(s) represent(s) the whole experience of the investigator (center) or is the selection method unclear to the extent that other patients with similar presentation may not have been reported? Yes 1
Ascertainment 2. Was the exposure adequately ascertained? Yes 1
3. Was the outcome adequately ascertained? Yes 1
4. Were other alternative causes that may explain the observation ruled out? Yes 1
Causality 5. Was there a challenge/rechallenge phenomenon? No 0
6. Was there a dose-response effect? No 0
7. Was follow-up long enough for outcomes to occur? Yes 1
Reporting 8. Is the case(s) described with sufficient details to allow other investigators to replicate the research or to allow practitioners make inferences related to their own practice? Yes 1
Total Score 6

The statistical analysis of data was performed with IBM SPSS for Windows, Version 13.0 (Armonk, New York, United States: IBM Corp). Continuous variables were tested for normality of distribution by the Kolmogorov-Smirnov test. For normally distributed values, descriptive results are presented as mean (standard deviation) and median while categorical variables are mentioned as numbers and percentages. The meta-regression analysis was performed using a random-effects model and stepwise selection of variables.13 To determine if the findings affected the severity of COVID-19, we used a meta-regression analysis using the following equations: Severity1=ß0+ß1*log1(lipase) and Severity2=ß0+ß1*log2(amylase).

RESULTS

The systematic search identified 71 possibly relevant records after review of the title, abstract or full text screening, and after exclusion of duplicates (Figure 1). Forty records were excluded after careful screening of the titles and abstracts, since they did not mention COVID-19 associated with acute pancreatitis presented as case reports or case series. Finally, we identified 31 articles (30 case reports and 1 case series of 2 cases), which included 32 cases of COVID-19 induced acute pancreatitis (Tables 2, 3, 4).14-44 Nineteen patients were females (59.4%) and 13 patients were males (40.6%). The median age was 53.5 years (range 20-76 years). The median age of the females was 52 years (range 20-76 years) (median 52) years and the median age of the males was 48 (24-68) years.

Figure 1.

Figure 1.

Flow diagram for study selection.

Table 2.

Demographic and clinical characteristics including COVID-19 severity and outcome of patients with COVID-19-induced acute pancreatitis.

# Author, Year Age/Gender Medical history Gastrointestinal manifestations Respiratory-general symptoms Severity of COVID-19 Outcome
1 Meyers, 202014 67/M Arterial hypertension
Cholecystectomy
Alcohol use
Abdominal pain Dyspnea
Fever
Severe Recovered
2 Karimzadeh, 202015 65/F Arterial hypertension
Asthma
Abdominal pain
Nausea
Dyspnea
Chills
Myalgia
Severe Recovered
3 Shinohara, 202016 58/M Arterial hypertension Abdominal pain Dyspnea
Fever
Critical Recovered
4 Rabice, 202017 36/F Pregnancy
Diabetes mellitus
Asthma Obesity
Abdominal pain
Nausea
Vomiting
Dry cough
Fever
Myalgia
Severe Recovered
5 Meireles, 202018 36/F Post-HELLP syndrome
Stage V chronic kidney disease
Arterial hypertension
Abdominal pain
Nausea
Vomiting
Dry cough
Dyspnea
Fever
Moderate Recovered
6 Fernandes, 202019 36/F No medical history Abdominal pain Dyspnea
Fever
Headache
Moderate Recovered
7 Alwaeli, 202020 30/M No medical history Abdominal pain
Nausea
Vomiting
Diarrhea
Dry cough
Dyspnea
Fever
Critical Recovered
8 Narang, 202021 20/F Pregnancy
Obesity
Cholocystectomy
Abdominal pain
Nausea
Vomiting
Dyspnea Critical Recovered
9 Kandasamy, 202022 45/F No medical history Abdominal pain
Nausea
Vomiting
Dyspnea Severe Recovered
10 Kumaran, 202023 67/F Laparotomy and small bowel resection and anastomosis of superior mesenteric artery stenosis
Arterial hypertension
Abdominal pain
Diarrhea
Vomiting
Dyspnea Severe Recovered
11 Acherjya, 202024 57/F Arterial hypertension Diabetes mellitus
Active malignancy of breast and larynx
Abdominal pain
Vomiting
No respiratory symptoms
Fever
Generalized body ache
Loss of smell
Fatigue
Arthralgia
Severe Recovered
12 Bokhari, 202025 32/M No medical history Abdominal pain
Vomiting
Productive cough
Fever
Myalgia
Mild Recovered
13 Mazrouei, 202026 24/M N/A Abdominal pain
Nausea
Vomiting
No respiratory-other symptoms Mild Recovered
14 Patnaik, 202027 29/M No medical history Abdominal pain Dyspnea
Fever
Moderate Recovered
15 Schepis, 202028 67/F Recent hospitalization for Interstitial
Edematous acute pancreatitis of unknown origin
Abdominal pain
Vomiting
No respiratory-other symptoms Mild Recovered
16 Aloysius, 202029 36/F Chronic anxiety
Obesity
Abdominal pain
Nausea
Vomiting
Diarrhea
Dry cough
Dyspnea
Fever
Critical Recovered
17 Gonzalo-Voltas, 202030 76/F Hypercholesterolemia
Gastroesophageal reflux
Abdominal pain
Vomiting
No respiratory-other symptoms Mild Recovered
18 Alves, 202031 56/F Arterial hypertension Abdominal pain Dry cough
Dyspnea
Fatigue
Critical Recovered
19 Ghosh, 202032 63/M Diabetes mellitus No Gastrointestinal Symptoms Dyspnea
Dry cough
Fever
Severe Recovered
20 Kataria, 202033 49/F No medical history Abdominal pain
Nausea
Vomiting
Dyspnea
Dry cough
Lethargy
Fever
Critical Recovered
21 Hadi, 202034 47/F No medical history Anorexia Dyspnea
Fever
Headache
Neck Pain
Sore Throat
Critical N/A
22 Hadi, 202034 68/F Arterial hypertension
Hypothyroidism
Osteoporosis
Abdominal pain
Vomiting
Diarrhea
Fever
Fatigue
Polydipsia
Critical N/A
23 Brikman, 202035 61/M No medical history Abdominal pain Dyspnea
Cough
Fever
Critical Recovered
24 Lakshmanan, 202036 68/M Nursing home resident
Diabetes mellitus
Arterial hypertension
Stage IV chronic kidney disease
Anorexia
Nausea
Vomiting
No respiratory-other symptoms Mild Recovered
25 Miao, 202037 26/F No medical history Abdominal pain
Vomiting
No respiratory symptoms Fever Mild Recovered
26 Pinte, 202038 47/M No medical history Abdominal pain
Nausea
Constipation
Lack of flatus
Dry cough Mild Recovered
27 Anand, 202039 59/F Cholecystectomy
Thrombophilia
Abdominal pain
Constipation
Cough
Fever
Sore Throat
Myalgia
Mild Recovered
28 Wifi, 202140 72/F Obesity
Arterial hypertension
Ischemic heart disease
Abdominal pain
Nausea
Vomiting
Cough
Nasal Sneezing
Severe Recovered
29 Mohammadi Arbati, 202141 28/M No medical history Abdominal pain
Nausea
Vomiting
Dyspnea
Dry cough
Fever
Myalgia
Critical Recovered
30 Maalouf, 202142 62/M Arterial hypertension
Diabetes mellitus
End-stage renal disease status
Post Kidney Transplant
Abdominal pain
Diarrhea
Vomiting
Anorexia
Dyspnea Moderate Recovered
31 AlHarm, 202143 52/F Diabetes mellitus
Arterial hypertension
Hypothyroidism
Obesity
Abdominal pain
Nausea
Vomiting
Dry cough
Dyspnea
Fever
Severe Recovered
32 Chivato Martín-Falquina, 202144 55/M No medical history No Gastrointestinal Symptoms Dyspnea Severe Recovered

HELLP: Hemolysis, Elevated Liver Enzymes, Low Platelet Count.

Table 3.

Laboratory and Imaging findings among the 32 cases following development of acute pancreatitis.

# Author, Year Lipase (U/L) Amylase (U/L) WBC/CRP Abdominal imaging features
1 Meyers, 202014 >3 times of UNL N/A N/A/N/A Abdominal CT: acute interstitial edematous pancreatitis.
2 Karimzadeh, 202015 >3 times of UNL <3 times of ULN Normal/N/A Abdominal CT: no abnormal findings.
3 Shinohara, 202016 N/A >3 times of UNL Normal/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
4 Rabice, 202017 >3 times of UNL <3 times of ULN Normal/N/A Abdominal CT was not recommended as it would not change clinical management.
5 Meireles, 202018 >3 times of UNL >3 times of UNL N/A/Elevated Angio-abdominal CT: exclusion of ischemic changes
6 Fernandes, 202019 >3 times of UNL >3 times of UNL N/A/N/A Abdominal CT: acute interstitial edematous pancreatitis.
7 Alwaeli, 202020 >3 times of UNL <3 times of ULN Normal/N/A Abdominal CT: acute interstitial edematous pancreatitis.
8 Narang, 202021 >3 times of UNL >3 times of UNL Elevated/N/A Abdominal MRI: acute interstitial edematous pancreatitis.
9 Kandasamy, 202022 >3 times of UNL >3 times of UNL Elevated/N/A Abdominal CT: acute interstitial edematous pancreatitis.
10 Kumaran, 202023 N/A >3 times of UNL Elevated/Elevated Abdominal CT: necrotizing pancreatitis
11 Acherjya, 202024 >3 times of UNL <3 times of UNL Decreased/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
12 Bokhari, 202025 >3 times of UNL >3 times of UNL Elevated/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
13 Mazrouei, 202026 >3 times of UNL >3 times of UNL N/A N/A Abdominal CT: acute interstitial edematous pancreatitis.
14 Patnaik, 202027 >3 times of UNL >3 times of UNL Elevated/Elevated Abdominal CT, Abdominal U/S : acute interstitial edematous pancreatitis and no evidence of common bile duct calculi.
15 Schepis, 202028 N/A >3 times of UNL Normal/N/A Abdominal CT: large pancreatic pseudocyst causing a partial stomach outlet obstruction
16 Aloysius, 202029 >3 times of UNL >3 times of UNL Normal/Elevated Abdominal CT: normal gall bladder, biliary tract, with unremarkable pancreas.
17 Gonzalo-Voltas, 202030 N/A >3 times of UNL Elevated/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
18 Alves, 202031 >3 times of UNL >3 times of UNL N/A/N/A Abdominal CT: acute interstitial edematous pancreatitis.
19 Ghosh, 202032 <3 times of UNL <3 times of UNL Normal/Elevated Abdominal CT: necrotizing pancreatitis
20 Kataria, 202033 >3 times of UNL >3 times of UNL Normal/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
21 Hadi, 202034 N/A >3 times of UNL Normal/Elevated Abdominal U/S: acute interstitial edematous pancreatitis.
22 Hadi, 202034 N/A >3 times of UNL Normal/Elevated N/A
23 Brikman, 202035 >3 times of UNL <3 times of UNL Elevated/N/A Abdominal CT: acute interstitial edematous pancreatitis.
24 Lakshmanan, 202036 >3 times of UNL >3 times of UNL Normal/Elevated Abdominal CT: acute interstitial edematous pancreatitis (peripancreatic fat stranding, greatest around the tail, with mild duodenal wall thickening and adjacent fat stranding)
25 Miao, 202037 >3 times of UNL N/A Normal/Elevated Abdominal CT, abdominal U/S: acute interstitial edematous pancreatitis.
26 Pinte, 202038 N/A N/A Elevated/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
27 Anand, 202039 N/A N/A Elevated/Elevated Abdominal CT: acute interstitial edematous pancreatitis.
28 Wifi, 202140 >3 times of UNL >3 times of UNL Elevated/Elevated Abdominal CT: without abnormal findings
29 Mohammadi Arbati, 202141 >3 times of UNL >3 times of UNL Elevated/Normal Abdominal CT: necrotizing pancreatitis
30 Maalouf, 202142 >3 times of UNL N/A Decreased/Elevated Abdominal MRI: necrotizing pancreatitis
31 AlHarm, 202143 N/A <3 times of UNL Elevated/Normal Abdominal CT: acute interstitial edematous pancreatitis.
32 Chivato Martín-Falquina, 202144 N/A >3 times of UNL N/A N/A Abdominal CT: acute interstitial edematous pancreatitis.

CRP: C-reactive protein; CT: Computerized tomography; MRI: Magnetic resonance imaging, U/S: Ultrasonography, ULN: Upper limit of normal, WBC: White blood cells.

Table 4.

Demographic and clinical data from the 32 cases.

Demographics
Gender
 Males 13/32 (59.4)
 Females 19/32 (40.6)
Gastrointestinal symptoms
 Abdominal pain 28/32 (87.5)
 Nausea 14/32 (43.8)
 Vomiting 20/32 (62.5)
 Diarrhea 5/32 (15.6)
 Constipation 2/32 (6.3)
 Anorexia 3/32 (9.3)
 Lack of flatus 1/32 (3.1)
 No gastrointestinal symptoms 2/32 (6.3)
Respiratory/General symptoms
 Dyspnea 20/32 (62.5)
 Cough 14/32 (43.8)
 Fever 19/32 (59.4)
 Myalgia 4/32 (12.5)
 Fatigue 3/32 (9.3)
 Headache 2/32 (6.3)
 No respiratory or general symptoms 4/32 (12.5)
 No respiratory symptoms 2/32 (6.3)
COVID-19 Severity
 Mild SARS-CoV-2 illness 8/32 (25)
 Moderate SARS-CoV-2 illness 4/32 (12.5)
 Severe SARS-CoV-2 illness 10/32 (31.2)
 Critical SARS-CoV-2 illness/Need for admission to ICU 10/32 (31.2)
Laboratory findings following development of acute pancreatitis
 Amylase levels over three times of ULN 20/27 (74.1)
 Amylase levels less than three times of ULN 7/27 (25.9)
 Lipase levels over three times of ULN 21/22 (95.5)
 Lipase levels less than three times of ULN 1/22 (0.5)
 Elevated white blood cell count 12/26 (46.2)
 White blood cell count with normal limits 12/26 (46.2)
 Decreased WBC count 2/26 (7.6)
 Elevated levels of CRP 18/20 (90)
 C-reactive protein levels within normal limits 2/20 (10)
Imaging features
 Acute interstitial edematous pancreatitis 21/31 (67.8)
 Necrotizing pancreatitis 4/31 (12.9)
 No abnormal imaging findings 3/31 (9.7)
 Abdominal CT was not performed due to pregnancy 1/31 (3.2)
 Angio-abdominal CT was conducted in order to exclude ischemic changes 1/31 (3.2)
 Large pancreatic pseudocyst causing a partial stomach outlet obstruction on abdominal CT 1/31 (3.2)
Medical history
 Arterial hypertension 11/31 (35.5)
 Diabetes mellitus 6/31 (19.4)
 Obesity 5/31 (16.1)
 Cholecystectomy 3/31 (9.7)
 Asthma 2/31 (6.5)
 Chronic kidney disease 3/31 (9.7)
 Osteoporosis 1/31 (3.2)
 Hypothyroidism 2/31 (6.5)
 Gastroesophageal reflux 1/31 (3.2)
 Hypercholesterolemia 1/31 (3.2)
 Active cancer of larynx and breast 1/31 (3.2)
 Thrombophilia 1/31 (3.2)
 Pregnancy 2/31 (6.5)
 No medical history 12/31 (38.5)
Outcomes
 Recovery 30/30 (100)
 Death 0

Data are n (%); ULN: Upper limit of normal.

The majority of the patients had abdominal pain as clinical manifestation (28/32, 87.5%). Other gastrointestinal symptoms were nausea, vomiting, diarrhea, constipation, anorexia and lack of flatus, while 2 (6.3%) of the patients presented with no gastrointestinal symptoms. Twenty (62.5%) patients presented with dyspnea and 14 (43.8%) presented with cough. A majority of patients had fever (59.4%). Four (12.5%) patients had no respiratory or general symptoms, while 2 (6.3%) patients had no respiratory symptoms. According to classification into severity of illness categories by National Institutes of Health (NIH),45 8 (25%) patients had mild SARS-CoV-2 illness, 4 (12.5%) patients had moderate SARS-CoV-2 illness, 10 (31.2%) patients had severe SARS-CoV-2 illness and 10 (31.2%) patients had critical SARS-CoV-2 illness (Table 4).

The data on serum amylase levels in 27 patients was over three times the upper limit of normal (ULN), while the rest had amylase levels less than three times of ULN. Data about lipase levels were available in 22 patients. The majority of these patients (21/22, 95.5%) had lipase levels over three times of ULN while only 1 patient (1/22, 0.5%) had lipase levels less than three times of ULN. Data about white blood cells (WBC) count were available in 26 patients. Twelve patients (12/26, 46.2%) had elevated WBC count, 12 (46.2%) had WBC count with normal limits while 2 (7.6%) had decreased WBC count. Data on C-reactive protein were available in 20 patients. Eighteen patients (90%) had elevated levels of CRP while 2 (10%) had CRP levels within normal limits. Imaging data were available in 31 patients (Table 4). Twenty-one (67.8%) of the patients had abdominal CT or MRI features compatible with acute interstitial edematous pancreatitis. Medical history data were available in 31 patients. Arterial hypertension was most common, followed by diabetes mellitus, obesity, cholecystectomy and others. Two female patients were pregnant while 12 patients (38.5%) had no medical history.

Data on outcome were available in 30 cases. All these patients recovered (30/30, 100%). In two cases, the outcome was unknown because the article was published while patients were still hospitalized.

The meta-regression analysis included the 30 articles that presented full laboratory findings following development of acute pancreatitis (Table 5). The R value of 0.461 represents the simple correlation, which indicates a moderate degree of correlation. The R2 value indicates how much of the total variation in severity, the dependent variable, was explained by the independent variables. In this case, R2 indicated that only 21.3% could be explained by the independent variables. The association of the regression model was statistically significant (i.e., a good fit for the data) (P<.05) (Tables 6 and 7).

Table 5.

Data for the meta-regression meta-analysis.

# Author, Year Age/Gender Severity of COVID-19 Lipase (U/L) Amylase (U/L)
1 Meyers, 202014 67/M Severe >3 times of UNL N/A
2 Karimzadeh, 202015 65/F Severe >3 times of UNL <3 times of ULN
3 Shinohara, 202016 58/M Critical N/A >3 times of UNL
4 Rabice, 202017 36/F Severe >3 times of UNL <3 times of ULN
5 Meireles, 202018 36/F Moderate >3 times of UNL >3 times of UNL
6 Fernandes, 202019 36/F Moderate >3 times of UNL >3 times of UNL
7 Aiwaeli, 202020 30/M Critical >3 times of UNL <3 times of ULN
8 Narang, 202021 20/F Critical >3 times of UNL >3 times of UNL
9 Kandasamy, 202022 45/F Severe >3 times of UNL >3 times of UNL
10 Kumaran, 202023 67/F Severe N/A >3 times of UNL
11 Acherjya, 202024 57/F Severe >3 times of UNL <3 times of UNL
12 Bokhari, 202025 32/M Mild >3 times of UNL >3 times of UNL
13 Mazrouei, 202026 24/M Mild >3 times of UNL >3 times of UNL
14 Patnaik, 202027 29/M Moderate >3 times of UNL >3 times of UNL
15 Schepis, 202028 67/F Mild N/A >3 times of UNL
16 Aloysius, 202029 36/F Critical >3 times of UNL >3 times of UNL
17 Gonzalo-Voltas, 202030 76/F Mild N/A >3 times of UNL
18 Alves, 202031 56/F Critical >3 times of UNL >3 times of UNL
19 Ghosh, 202032 63/M Severe <3 times of UNL <3 times of UNL
20 Kataria, 202033 49/F Critical >3 times of UNL >3 times of UNL
21 Hadi, 202034 47/F Critical N/A >3 times of UNL
22 Hadi, 202034 68/F Critical N/A >3 times of UNL
23 Brikman, 202035 61/M Critical >3 times of UNL <3 times of UNL
24 Lakshmanan, 202036 68/M Mild >3 times of UNL >3 times of UNL
25 Miao, 202037 26/F Mild >3 times of UNL N/A
26 Pinte, 202038 47/M Mild N/A N/A
27 Anand, 202039 59/F Mild N/A N/A
28 Wifi, 202140 72/F Severe >3 times of UNL >3 times of UNL
29 Mohammadi Arbati, 202141 28/M Critical >3 times of UNL >3 times of UNL
30 Maalouf, 202142 62/M Moderate >3 times of UNL N/A
31 AlHarm, 202143 52/F Severe N/A <3 times of UNL
32 Chivato Martin-Falquina, 202144 55/M Severe N/A >3 times of UNL

ULN: Upper limit of normal

Table 6.

Results of the regression analysis for lipase (n=24).

Parameter Beta estimate z P
ß0 −.484 −.780 .442
ß1 .753 2.072 .124

Severity1=−,484+753*log1(lipase)

Table 7.

Results of the regression analysis for amylase lipase (n=27).

Parameter Beta estimate z P
ß0 −.484 −.780 .442
ß1 1.223 1.586 .042

Severity2=−,484+1,1223*log2(amylase)

DISCUSSION

There are very few case reports and case series describing COVID-19 induced acute pancreatitis. To our knowledge, we present the largest and most comprehensive systematic review of case reports and case series on SARS-CoV-2 infection causing acute pancreatitis. The ages of the patients were uniformly distributed with a median age of 53.5 years. The majority of the patients were females. Lipase and amylase were greater than three times the ULN while WBC counts and CRP were elevated in the most of the cases. The majority of the patients mentioned abdominal pain while other frequent symptoms were nausea and vomiting. The most common respiratory symptoms were dyspnea and cough. Fever was the most frequent general symptom and in some cases neither respiratory nor general symptoms were present. Most of the patients experienced severe and critical SARS-CoV-2 illness. The imaging features of abdominal CT were mostly compatible with acute interstitial edematous pancreatitis. The most frequent comorbidity was arterial hypertension and 38.5% of the patients had no medical history. In addition, where data were available, all the patients recovered.

The results of meta-regression analysis showed a low heterogeneity between the studies regarding the severity of COVID-19 disease and that serum levels of lipase and amylase had a moderate positive correlation with the severity of COVID-19 disease.

Data from studies about COVID-19 patients presenting with acute pancreatitis are limited. Szatmary et al in a study of hospitalized patients for acute pancreatitis found only 5 patients with SARS-CoV-2 infection in whom other causes of acute pancreatitis were excluded. All the patients were young adult males with a median age of 42 years and all were obese with no history of cardiovascular disease. There were no data about serum lipase levels; serum amylase levels were increased. Abdominal CT was used to establish the final diagnosis. The finding of pancreatic inflammation on CT was mild pancreatic edema without pancreatic or peripancreatic necrosis, compatible with acute interstitial edematous pancreatitis. In this study, all patients with COVID-19 associated acute pancreatitis recovered.46

Our systematic review was written after a comprehensive search of the literature with specific criteria for inclusion and quality assessment. However, our results are limited by the quality and extent of the data in the reports. More specifically, case series and case reports are unchecked, and while they can recommend hypotheses they are not able to confirm robust associations. Clinicians should be aware of the few cases reported in the literature, suggesting that acute pancreatitis can result from COVID-19. While case reports can provide signals, they are not strong enough for statistical inference. Thus, the evidence provided is insufficient to suggest systematic screening in patients with COVID-19 for pancreatic involvement, but should alert physicians of possible pancreatic involvement by SARS-CoV-2.

In conclusion, COVID-19 associated acute pancreatitis affected mostly females with a median age of 53.5 years. Concerning laboratory findings, lipase and amylase were greater than three times the ULN while WBC counts and CRP were elevated in the most of the cases. The most frequent gastrointestinal, respiratory and general symptom was abdominal pain, dyspnea and fever, respectively. The most common imaging feature was acute interstitial edematous pancreatitis and the most frequent comorbidity was arterial hypertension while several patients had no medical history. The outcome was favorable despite the fact that most of the patients experienced severe and critical illness. Our results warrant the need for larger controlled research to detect acute pancreatitis during COVID-19 course and to provide data on patient characteristics and outcomes.

Funding Statement

Funding: None.

REFERENCES

  • 1.Lankisch PG, Apte M, Banks PA. Acute pancreatitis. Lancet. 2015;386(9988):85–96. [DOI] [PubMed] [Google Scholar]
  • 2.Greenberg JA, Hsu J, Bawazeer M, Marshall J, Friedrich JO, Nathens A, et al. Clinical practice guideline: management of acute pancreatitis. Can J Surg. 2016;59(2):128–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Rawla P, Bandaru SS, Vellipuram AR. Review of Infectious Etiology of Acute Pancreatitis. Gastroenterology Res. 2017;10(3):153–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Gupta V. COVID-19 and Acute Pancreatitis: What Do Surgeons Need to Know? Indian J Surg. 2020:1–4. [DOI] [PMC free article] [PubMed]
  • 5.Su S, Wong G, Shi W, Liu J, Lai ACK, Zhou J, et al. Epidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses. Trends Microbiol. 2016;24(6):490–502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Liu F, Long X, Zhang B, Chen X, Zhang Z. ACE2 Expression in Pancreas May Cause Pancreatic Damage After SARS-CoV-2 Infection. Clin Gastroenterol Hepatol. 2020;18(9):2128–2130.e2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Banks PA. Epidemiology, natural history, and predictors of disease outcome in acute and chronic pancreatitis. Gastrointest Endosc. 2002. Dec;56(6 Suppl):S226–30. [DOI] [PubMed] [Google Scholar]
  • 8.Incidence of coronavirus (COVID-19) cases in Europe as of June 12, 2022, by country. 2022, Cited: July 23. Available from: https://www.statista.com/statistics/1110187/coronavirus-incidence-europe-by-country/
  • 9.Systematic Reviews: What is a systematic review? [Internet]. Curtain University. Cited July 2022: https://libguides.library.curtin.edu.au/systematic-reviews [Google Scholar]
  • 10.Banks PA, Bollen TL, Dervenis C, Gooszen HG, Johnson CD, Sarr MG, et al. Acute Pancreatitis Classification Working Group. Classification of acute pancreatitis–2012: revision of the Atlanta classification and definitions by international consensus. Gut. 2013;62(1):102–11. [DOI] [PubMed] [Google Scholar]
  • 11.Murad MH, Sultan S, Haffar S, Bazerbachi F. Methodological quality and synthesis of case series and case reports. BMJ Evid Based Med. 2018;23(2):60–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Borenstein M, Hedges LV, Higgins JP, Rothstein HR. A basic introduction to fixed-effect and random-effects models for meta-analysis. Res Synth Methods. 2010;1(2):97–111. doi: 10.1002/jrsm.12. [DOI] [PubMed] [Google Scholar]
  • 14.Meyers MH, Main MJ, Obstein KL. A Case of COVID-19-Induced Acute Pancreatitis. Pancreas. 2020;49(10):e108–e109. [DOI] [PubMed] [Google Scholar]
  • 15.Karimzadeh S, Manzuri A, Ebrahimi M, Huy NT. COVID-19 presenting as acute pancreatitis: Lessons from a patient in Iran. Pancreatology. 2020;20(5):1024–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Shinohara T, Otani A, Yamashita M, Wa-kimoto Y, Jubishi D, Okamoto K, et al. Acute Pancreatitis During COVID-19 Pneumonia. Pancreas. 2020;49(10):e106–e108. [DOI] [PubMed] [Google Scholar]
  • 17.Rabice SR, Altshuler PC, Bovet C, Sullivan C, Gagnon AJ. COVID-19 infection presenting as pancreatitis in a pregnant woman: A case report. Case Rep Womens Health. 2020;27:e00228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Meireles PA, Bessa F, Gaspar P, Parreira I, Silva VD, Mota C, et al. Acalculous Acute Pancreatitis in a COVID-19 Patient. Eur J Case Rep Intern Med. 2020;7(6):001710. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Fernandes DA, Yumioka AS, Filho HRM. SARS-CoV-2 and acute pancreatitis: a new etiological agent? Rev Esp Enferm Dig. 2020;112(11):890. [DOI] [PubMed] [Google Scholar]
  • 20.Alwaeli H, Shabbir M, Khamissi Sobi M, Alwaeli K. A Case of Severe Acute Pancreatitis Secondary to COVID-19 Infection in a 30-Year-Old Male Patient. Cureus. 2020;12(11):e11718. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Narang K, Szymanski LM, Kane SV, Rose CH. Acute Pancreatitis in a Pregnant Patient With Coronavirus Disease 2019 (COVID-19). Obstet Gynecol. 2020;Publish Ahead of Print. [DOI] [PMC free article] [PubMed]
  • 22.Kandasamy S. An unusual presentation of COVID-19: Acute pancreatitis. Ann Hepatobiliary Pancreat Surg. 2020;24(4):539–41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Kumaran NK, Karmakar BK, Taylor OM. Coronavirus disease-19 (COVID-19) associated with acute necrotising pancreatitis (ANP). BMJ Case Rep. 2020;13(9):e237903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Acherjya GK, Rahman MM, Islam MT, Alam AS, Tarafder K, Rahman MM, et al. Acute pancreatitis in a COVID-19 patient: An unusual presentation. Clin Case Rep. 2020;8(12):3400–3407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Bokhari SMMA, Mahmood F. Case Report: Novel Coronavirus-A Potential Cause of Acute Pancreatitis? Am J Trop Med Hyg. 2020;103(3):1154–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Mazrouei SSA, Saeed GA, Al Helali AA. COVID-19-associated acute pancreatitis: a rare cause of acute abdomen. Radiol Case Rep. 2020;15(9):1601–3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Patnaik RNK, Gogia A, Kakar A. Acute pancreatic injury induced by COVID-19. ID-Cases. 2020;22:e00959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Schepis T, Larghi A, Papa A, Miele L, Panzuto F, De Biase L, et al. SARS-CoV2 RNA detection in a pancreatic pseudocyst sample. Pancreatology. 2020;20(5):1011–2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Aloysius MM, Thatti A, Gupta A, Sharma N, Bansal P, Goyal H. COVID-19 presenting as acute pancreatitis. Pancreatology. 2020;20(5):1026–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Gonzalo-Voltas A, Fernández-Pérez-Torres CU, Baena-Díez JM. Acute pancreatitis in a patient with COVID-19 infection. Med Clin (Barc). 2020;155(4):183–4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Alves AM, Yvamoto EY, Marzinotto MAN, Teixeira ACS, Carrilho FJ. SARS-CoV-2 leading to acute pancreatitis: an unusual presentation. Braz J Infect Dis. 2020;24(6):561–4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Ghosh A, Gupta V, Misra A. COVID19 induced acute pancreatitis and pancreatic necrosis in a patient with type 2 diabetes. Diabetes Metab Syndr. 2020;14(6):2097–8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kataria S, Sharif A, Ur Rehman A, Ahmed Z, Hanan A. COVID-19 Induced Acute Pancreatitis: A Case Report and Literature Review. Cureus. 2020;12(7):e9169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Hadi A, Werge M, Kristiansen KT, Pedersen UG, Karstensen JG, Novovic S, et al. Coronavirus Disease-19 (COVID-19) associated with severe acute pancreatitis: Case report on three family members. Pancreatology. 2020;20(4):665–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Brikman S, Denysova V, Menzal H, Dori G. Acute pancreatitis in a 61-year-old man with COVID-19. CMAJ. 2020;192(30):E858–E859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Lakshmanan S, Malik A. Acute Pancreatitis in Mild COVID-19 Infection. Cureus. 2020;12(8):e9886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Miao Y, Lidove O, Mauhin W. First case of acute pancreatitis related to SARS-CoV-2 infection. Br J Surg. 2020;107(8):e270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Pinte L, Baicus C. Pancreatic involvement in SARS-CoV-2: case report and living review. J Gastrointestin Liver Dis. 2020;29(2):275–6. [DOI] [PubMed] [Google Scholar]
  • 39.Anand ER, Major C, Pickering O, Nelson M. Acute pancreatitis in a COVID-19 patient. Br J Surg. 2020;107(7):e182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Wifi MN, Nabil A, Awad A, Eltatawy R. COVID-induced pancreatitis: case report. Egypt J Intern Med. 2021;33(1):10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Mohammadi Arbati M, Molseghi MH. COVID-19 Presenting as Acute Necrotizing Pancreatitis. J Investig Med High Impact Case Rep. 2021;9:23247096211009393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Maalouf RG, Kozhaya K, El Zakhem A. SARS-CoV-2 induced necrotizing pancreatitis. Med Clin (Barc). 2021;S0025-7753(21)00025-7. [DOI] [PMC free article] [PubMed]
  • 43.AlHarmi RAR, Fateel T, Sayed Adnan J, AlAwadhi K. Acute pancreatitis in a patient with COVID-19. BMJ Case Rep. 2021;14(2):e239656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Chivato Martín-Falquina I, García-Morán S, Jiménez Moreno MA. Acute pancreatitis in SARS-CoV-2 infection. Beyond respiratory distress. Rev Esp Enferm Dig. 2021: Epub ahead of print. [DOI] [PubMed]
  • 45.Clinical Spectrum of SARS-CoV-2 Infection. 2022, Cited: July 23 https://www.covid19treatmentguidelines.nih.gov/overview/clinical-spectrum/
  • 46.Szatmary P, Arora A, Thomas Raraty MG, Joseph Dunne DF, Baron RD, Halloran CM. Emerging Phenotype of Severe Acute Respiratory Syndrome-Coronavirus 2-associated Pancreatitis. Gastroenterology. 2020. Oct;159(4):1551–4 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Annals of Saudi Medicine are provided here courtesy of King Faisal Specialist Hospital and Research Centre

RESOURCES