Acalculous Cholecystitis

Article Author:
Mark Jones
Article Editor:
Troy Ferguson
Updated:
10/25/2019 3:02:02 PM
PubMed Link:
Acalculous Cholecystitis

Introduction

Acalculous cholecystitis is a form of cholecystitis caused by dysfunction or hypokinesis of gallbladder emptying. The more commonly encountered condition of cholecystitis is caused by a mechanical blockage of the gallbladder outlet at the cystic duct, usually by a gallstone. Duncan first described the condition of acalculous cholecystitis in 1844. Although it can present acutely, acalculous cholecystitis typically presents more insidiously. The condition is more common in ill patients in the ICU. Acalculous cholecystitis is a life-threatening disorder that has a high risk of perforation and necrosis compared to the more typical calculous disease.[1][2][3]

Etiology

Many different factors can cause gallbladder dysfunction. Long periods of fasting, total parenteral nutrition (TPN), and drastic weight loss can all increase the incidence of acalculous cholecystitis. Often other more serious conditions are present. Patients in the intensive care unit or those recovering from major surgeries or other serious ailments such as a stroke, heart attack, sepsis, severe burns, and extensive trauma are all at a higher risk to develop acalculous cholecystitis. Gallbladder stasis secondary to lack of gallbladder stimulation leads to concentration of the bile salts with a build-up of pressure within the organ. This leads to ischemia, pressure necrosis and eventual perforation. This static condition also increases seeding and growth of enteric pathogens such as Escherichia coli, Klebsiella, Bacteroides, Proteus, Pseudomonas, and Enterococcus faecalis. Individuals with chronic acalculous cholecystitis may have decreased function of gallbladder emptying, hypokinetic biliary dyskinesia. This may be from a variety of factors including hormone related, vasculitis, and decreased nerve innervation from conditions such as diabetes. Often the exact etiology of chronic acalculous cholecystitis is unknown.[4][5]

Epidemiology

Acalculous cholecystitis accounts for ten percent of all cases of acute cholecystitis and 5% to 10% of all cases of cholecystitis. It has an equal predisposition between males and females. However, males are more likely to develop acute acalculous cholecystitis after surgery. Rates are increased in HIV and other immunosuppressed patients. These individuals are more susceptible to certain opportunistic infections such as microsporidia, cytomegalovirus (CMV), and Cryptosporidium, which can seed and flourish in bile within the gallbladder. Carriers of Giardia lamblia, Helicobacter pylori, and Salmonella typhi are also associated with increased risks to develop cholecystitis.[6][7]

Pathophysiology

Stasis of the gallbladder results in the build-up of intraluminal pressure. This eventually results in ischemia of the gallbladder wall and inflammation. This stasis can also lead to the colonization of bacteria which contributes to the inflammatory response. If the pressure is not relieved, the gallbladder wall will become progressively ischemic eventually resulting in gangrenous changes and perforation. This will lead to sepsis and shock. These findings are referred to as acute cholecystitis. Chronic acalculous cholecystitis usually presents more insidiously. Symptoms are more prolonged and may be less severe. Symptoms may also be more intermittent and vague, although patients can present with signs of acute biliary colic.[6][8]

Histopathology

There are varying degrees of inflammation found with acalculous cholecystitis. Findings are similar to calculus cholecystitis, only with an absence of gallstones. The gallbladder wall will be thickened to variable degrees, and there may be adhesions to the serosal surface. Smooth muscle hypertrophy, especially in chronic conditions, is present. At times sludge or very viscous bile can be seen. These findings are usual precursors to gallstones and are formed from increased biliary salts or stasis. Various species of bacteria can be present in 11% to 30% of the cases. Rokitansky-Aschoff sinuses are present 90% of the time in cholecystitis specimens. These are a herniation of intraluminal sinuses from increased pressures possibly associated with ducts of Luschka. The mucosa will exhibit varying degrees of inflammation from mild to ulcerations with gangrenous changes. Extreme situations may show total gangrenous changes of the gallbladder with perforation.[9]

Toxicokinetics

Mild cases of acalculous cholecystitis are usually only treated for symptoms of biliary colic. Cases of acute cholecystitis can lead to sepsis and shock. The pressurized intraluminal gallbladder bile can be susceptible to bacterial seeding. Antibiotics are usually ineffective due to the increased intraluminal pressure and compromise of the intraluminal blood supply. Eventual perforation will lead to bile peritonitis and contribute to the shock condition. The release of inflammatory byproducts also contributes to shock and susceptibility to sepsis.

History and Physical

Mild acalculous cholecystitis may present similarly to calculous cholecystitis. Patients may have right upper quadrant abdominal pain, reproduced with deep palpation (Murphy's sign). Nausea, food intolerances, bloating, and belching may also be present. Signs of acute acalculous cholecystitis exhibit an abrupt onset of symptoms of severe right upper abdominal pain. There may be a palpable distended gallbladder. These patients present as being very ill, possibly septic and are in an ICU setting. Their white blood cell count is usually, but not always, elevated. Often they have been in the hospital for other significant illnesses or are recovering from major surgery.

Evaluation

The test of choice for chronic acalculous cholecystitis is a cholescintigraphy nuclear scan (HIDA) with the administration of cholecystokinin (CCK). This study examines the function of the gallbladder. After the radionuclide is administered, CCK is given to stimulate the gallbladder to empty. A calculated ejection fraction of 35% or less may be indicative of hypokinetic functioning of the gallbladder. An ultrasound of the gallbladder may also be useful. If this shows a thickened gallbladder wall of over 3.5 mm, this may be due to cholecystitis.

Blood work is not diagnostic but will reveal an elevated WBC and abnormal liver function tests.

The diagnosis of acute acalculous cholecystitis can often be made with an ultrasound of the abdomen. The gallbladder will show a significantly thickened wall with edema and possible pericholecystic fluid. CT scans may also make this diagnosis. If there is still uncertainty of the diagnosis, then a HIDA scan can be done. Acute cholecystitis will result in no filling of the gallbladder with the radionuclide material.[5][10]

Treatment / Management

Patients with acalculous cholecystitis are very ill and need to be stabilized before any procedure can be done. In those patients who are unstable, one may consider the placement of a percutaneous drainage tube in the gallbladder by the radiologist. Another option is Stent placement via ERCP to decompress the gallbladder. 

Chronic acalculous cholecystitis is treated the same as cholecystitis with stones. Laparoscopic cholecystectomy is the treatment of choice. An open cholecystectomy can also be performed if there is a contraindication to laparoscopic surgery. Acute cholecystitis must be addressed fairly urgently because rapid progression and deterioration may result if untreated. The best definitive therapy is cholecystectomy, either laparoscopic or open. If the patient is too unstable to undergo major surgery, then percutaneous drainage is needed with possible definitive cholecystectomy at a later date. Administration of broad-spectrum antibiotics is routinely done. However, this is usually not effective. There is minimal penetration of antibiotics into the pressurized gallbladder, but they will help treat any systemic bacteremia.[4][11][12]

Differential Diagnosis

  • Cholangitis
  • Acute cholecystitis
  • Pancreatitis
  • Hepatitis

Prognosis

Acalculous cholecystitis is a serious illness that has high morbidity and mortality. The reported mortality of the condition varies from 30--50% depending on the age of the patient. Even those who survive have a long recovery that can take months.

Complications

  • Perforation of the gallbladder
  • Gangrene of the gallbladder
  • Sepsis

Postoperative and Rehabilitation Care

Most patients are kept NPO until the clinical status has improved. Thus, IV hydration is necessary

Consultations

  • General surgeon
  • Gastroenterologist
  • Radiologist

Enhancing Healthcare Team Outcomes

Acalculous cholecystitis is a life-threatening disorder that can rapidly prove fatal. Most patients are old, frail and have many comorbidities. Because of the complexity in management, the condition is best managed by an interprofessional team that includes the following:

Patients with acalculous cholecystitis are often very ill and need ICU monitoring. The nurses looking after these patients must have a high suspicion of the disorder because often the signs and symptoms of sepsis are vague. Fluid intake and output have to be closely monitored together with the respiratory status. These patients need DVT and peptic ulcer prophylaxis and incentive spirometry.

Because the patients are kept NPO, a dietary consult should be requested to determine the need for IV nutrition.

The radiologist must be aware of the patient's admission because percutaneous drainage of the gallbladder may be urgently required. The gastroenterologist may need to perform an endoscopy to place a stent at the ampulla of Vater to decompress the gallbladder.

Because patients are frail, bedside physical therapy is needed to regain muscle function and strength.

Finally, the general surgeon may need to perform an urgent cholecystectomy in patients with gangrene.

Outcomes

The outcome of patients with acalculous cholecystitis is guarded. Over the years the mortality of acalculous cholecystitis has decreased but still remains about 10% despite optimal treatment. These patients often develop fulminant sepsis, ARDS, multiorgan failure and also have a high incidence of adverse cerebrovascular events. Most case reports indicate poor outcomes and even patients who survive have a prolonged recovery period but never attain full functional recovery.[10][13] (Level V)


References

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[2] Kwatra NS,Nurko S,Stamoulis C,Falone AE,Grant FD,Treves ST, Chronic Acalculous Cholecystitis in Children with Biliary Symptoms: Usefulness of Hepato-Cholescintigraphy. Journal of pediatric gastroenterology and nutrition. 2018 Sep 25     [PubMed PMID: 30256266]
[3] Iqbal S,Khajinoori M,Mooney B, A case report of acalculous cholecystitis due to {i}Salmonella paratyphi{/i} B. Radiology case reports. 2018 Dec     [PubMed PMID: 30233740]
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[6] Yi DY,Chang EJ,Kim JY,Lee EH,Yang HR, Age, Predisposing Diseases, and Ultrasonographic Findings in Determining Clinical Outcome of Acute Acalculous Inflammatory Gallbladder Diseases in Children. Journal of Korean medical science. 2016 Oct     [PubMed PMID: 27550491]
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[8] Le Bail B, [Pathology of gallbladder and extrahepatic bile ducts. Case 1. Alcalculous gangrenous cholecystitis]. Annales de pathologie. 2014 Aug     [PubMed PMID: 25132438]
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[10] Noh SY,Gwon DI,Ko GY,Yoon HK,Sung KB, Role of percutaneous cholecystostomy for acute acalculous cholecystitis: clinical outcomes of 271 patients. European radiology. 2018 Apr     [PubMed PMID: 29116391]
[11] Soria Aledo V,Galindo Iñíguez L,Flores Funes D,Carrasco Prats M,Aguayo Albasini JL, Is cholecystectomy the treatment of choice for acute acalculous cholecystitis? A systematic review of the literature. Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva. 2017 Oct     [PubMed PMID: 28776380]
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