Acute pancreatitis following coronary artery angiography

Background

Coronary artery disease is the most common cardiovascular disease. It is also the leading cause of death in Switzerland.1 Approximately 23 000 diagnostics and/or therapeutic coronary artery angiographies were performed in Switzerland in 2016. This rate is rising steadily, with an average of approximately 1000 additional angiographies per year.2

Access point complications (infection and pseudoaneurysm), cardiac complications (arrhythmias, dissection of the coronary arteries and stenosis of the stent), hypersensitivity to contrast agent, acute renal failure and cholesterol embolism are well-documented complications.

In this report, we describe a case of severe pancreatitis following coronary angiography and discuss its possible physiopathology.

Case presentation

A 71-year-old female patient was admitted to hospital for elective coronary angiography motivated by septal hypokinesis visualised on transthoracic cardiac ultrasound. This examination was performed 3 months prior to admission as a part of the assessment of a transient cerebral ischaemic attack. On admission, she reported dyspnoea on exertion without chest pain. Her medical history was notable for hypertension, hypothyroidism, history of kidney lithiasis and gallbladder lithiasis requiring cholecystectomy at the age of 49 years, and the cited transient ischaemic attack. She reported occasional alcohol consumption (one glass of wine every month). There was no reported abdominal pain or recent abdominal trauma. Family history did not include recurrent or childhood pancreatitis. Current medications were acetylsalicylic acid, atorvastatin, candesartan, amlodipine, levothyroxine and cholecalciferol.Through a radial approach, 225 mL of iodixanol contrast agent (Visipaquem) was injected. During the coronary artery angiography, tritroncular coronary disease was revealed, requiring the placement of two active stents on the right coronary artery. Intermediate stenosis of the interventricular artery will be treated in a second stage. During a scan time of 18 min, the patient received a total of 7000 IU of unfractionated heparin, 5 mg verapamil, 5 mg adenosine and sedation with 2 mg midazolam and 2 mg morphine.

A few minutes after the procedure, she experienced sudden epigastric pain of intensity 8/10, with radiation to the back associated with vomiting food without haematemesis. She was, therefore, admitted to the internal medicine department for further investigation.

On physical examination, vital signs were normal, and the body mass index was 29 kg/m². The right wrist showed no haematoma and radial pulse was present. Abdominal examination showed tenderness in the epigastrium with mild guarding. No jaundice was noted. The remainder of the examination, including cardiopulmonary examination, was unremarkable.

Investigations

Laboratory studies showed a leucocyte count of 20×10⁹/L with a C reactive protein of 22 mg/L. The serum lipase was elevated at 267 U/L. Liver tests showed cholestasis without significant cytolysis (γ-glutamyltranspeptidase 173 U/L, alkaline phosphatase 119 U/L, total bilirubin 4 μmol/L, aspartate aminotransferase 43 U/L and alanine aminotransferase 56 U/L). Serum creatinine level was within normal range. Corrected calcium, triglycerides and IgG4 were within the normal range. Lipid profile (low-density lipoprotein 1.99 mmol/L, high-density lipoprotein 2.5 mmol/L and total cholesterol 3.8 mmol/L) was within normal range too.

Electrocardiogram showed a regular sinus rhythm without any repolarisation disorder.

Abdominal ultrasound performed immediately showed biliary tract ectasia probably related to the history of cholecystectomy. There were no calculi visualised on the cholangio-MRI performed after 7 days. An abdominal contrast-enhanced CT performed after 48 hours of the presentation showed acute Balthazar C pancreatitis with necrosis within the head and uncinate process, and a necrotic collection along the right paracolic gutter (figure 1).

Figure 1

Abdominal scan showing an area of necrosis (☆) within the head of the pancreas.

The 2-month control cholangio-MRI showed no obstructive calculi, stable bile duct ectasia and also excluded a tumour of the pancreas (figure 2).

Figure 2

Abdominal MRI showing bile duct ectasia.

Diagnosis of Balthazar C pancreatitis of undetermined origin was retained.

Treatment

A supportive treatment was initiated with intravenous hydration and WHO level II analgesia. The patient fasted for 5 days (abdominal pain and nausea) with a gradual return to a low-fat diet.

Outcome and follow-up

The evolution was complicated by fever up to 38.5°C persisting for 5 days without haemodynamic instability. Laboratory studies showed accentuation of the inflammatory syndrome (C reactive protein up to 204 mg/L). The patient received antibiotics for a total duration of 14 days (ceftriaxone/metronidazole for 7 days and then ciprofloxacin/metronidazole), without microbiological evidence of infection. There was no organ dysfunction, cholestasis remained stable and the lipase decreased progressively with biological monitoring over 3 days. Hospitalisation lasted 3 weeks.

Six months later, the patient underwent another coronary angiography due to new-onset chest pain, this time without further complication. The contrast product was the same, but at a lower dosage than the first time (160 mL).