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LETTER TO EDITOR
Year : 2010  |  Volume : 42  |  Issue : 3  |  Page : 193-194
 

Biliary pseudolithiasis secondary to ceftriaxone therapy


Department of Pediatrics, Lokmanya Tilak Municipal General Hospital, Mumbai, India

Date of Web Publication28-Jul-2010

Correspondence Address:
Syed Ahmed Zaki
Department of Pediatrics, Lokmanya Tilak Municipal General Hospital, Mumbai
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0253-7613.66847

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How to cite this article:
Zaki SA, Shanbag P. Biliary pseudolithiasis secondary to ceftriaxone therapy. Indian J Pharmacol 2010;42:193-4

How to cite this URL:
Zaki SA, Shanbag P. Biliary pseudolithiasis secondary to ceftriaxone therapy. Indian J Pharmacol [serial online] 2010 [cited 2020 Sep 25];42:193-4. Available from: http://www.ijp-online.com/text.asp?2010/42/3/193/66847


Sir,

Ceftriaxone is a third-generation cephalosporin widely used for the treatment of a variety of bacterial infections in children. [1] It has a broad-spectrum antibacterial activity with a long plasma half-life that permits reduced dosing schedules as compared to other cephalosporins and penicillins. [2] These factors have lead to its increased use in public hospitals in developing countries. As this antibiotic becomes more commonly prescribed, practitioners should be aware of the potential adverse-effects of the drug, especially if the adverse-event can lead to medically inappropriate interventions. We herein report nine cases of biliary pseudolithiasis secondary to ceftriaxone therapy seen at our institution.

There were nine children admitted between January to October 2009 who developed biliary pseudolithiasis after starting ceftriaxone therapy. The clinical and demographic characteristics of the patients are shown in [Table 1]. None of the patients had hemolytic anemia, renal or liver failure, cystic fibrosis or malignancy or had received total parenteral nutrition. None of them were taking other drugs known to be associated with biliary sludge and/or lithiasis. Complete blood count, reticulocyte count, serum calcium, liver and renal function tests were normal in these children. Their family and past history was unremarkable. All patients had received intravenous ceftriaxone (100 mg/kg/day) in two divided doses. Six patients developed abdominal pain within 1 week of starting ceftriaxone therapy and three patients developed abdominal pain after completion of their therapy, i.e. after 10 days. The abdominal pain was colicky, in the right hypochondriac region and without any aggravating or relieving factors. Ultrasonography of the abdomen was performed in all these symptomatic patients [Table 2]. Patients who developed biliary pseudolithiasis before completion of treatment were shifted to alternative therapy. All the patients responded within 1 week of stopping ceftriaxone therapy, with the ultrasonography showing no evidence of pseudolithiasis. Rechallenge with ceftriaxone was not carried out in our patients due to ethical constraints. This can be labelled as a type A class of adverse-effect. It can be considered as probable/likely adverse drug reaction as per causality assessment of suspected adverse drug reaction. [3]

The first sonographic demonstration of precipitates forming in the gallbladder during ceftriaxone therapy was reported by Schaad et al. in 1986. [4] In subsequent reports, biliary sludge or biliary pseudolithiasis has frequently been reported with this antibiotic. [5] Ceftriaxone is mainly excreted in the urine and a significant proportion (40%) is also secreted in the bile and then eliminated via the gastrointestinal tract. [2] It is secreted unmetabolized into bile in concentrations 20-150-times that of serum concentrations and is further concentrated in the gall bladder as a calcium salt. [6] When the solubility of the drug exceeds, it leads to the formation of calcium-ceftriaxone salt precipitates that mimic gallstone on ultrasonography. With discontinuation of the drug, these "stones" resolve spontaneously, a phenomenon termed "reversible ceftriaxone biliary pseudolithiasis." [7] The incidence of pseudolithiasis in children treated with ceftriaxone is up to 25%, but only a minority of these patients become symptomatic. [2] Papadopoulou et al. described 25% of children on high-dose ceftriaxone therapy (>100 mg/kg per day) developing pseudolithiasis, with only 4% having right-upper quadrant pain in association with these ultrasonographic changes. [5] Precipitates form after 4-22 days (mean, 9 days) of treatment and resolve within 2-63 days (mean, 15 days) after cessation of therapy. [8] Risk factors for biliary pseudolithiasis formation include age greater than 24 months, gram-negative sepsis, high doses of ceftriaxone (≥2 g/day), increased calcium secretion into bile (e.g., hypercalcemia), post surgery, decreased bile flow (e.g., fasting or total parenteral nutrition) and increased ceftriaxone excretion in bile (e.g., renal failure or long-term treatment with ceftriaxone). [2],[6] Conservative management of ceftriaxone-associated "pseudolithiasis" is suggested in managing this clinical entity with serial ultrasounds until complete resolution of "stone" formation. [2]

In conclusion, patients receiving a high dose of ceftriaxone and developing colicky abdominal pain should be considered for ultrasound and a change in antibiotic if appropriate. Recognition of this complication will prevent unnecessary surgical interventions.


 » Acknowledgment Top


We would like to thank Dr. Sandhya Kamath, Dean of our institution, for permitting us to publish this manuscript.

 
 » References Top

1.De Moor RA, Egberts GC, Schroder CH. Ceftriaxone-associated nephrolithiasis and biliary pseudolithiasis. Eur J Pediatr 1999;158:975-7.  Back to cited text no. 1      
2.Lemberg D, Day AS, Wyeth B. Biliary colic: Is it gallstones? J Paediatr Child Health 2005;41:291-3.  Back to cited text no. 2  [PUBMED]  [FULLTEXT]  
3.Edwards IR, Aronson JK. Adverse drug reactions: Definitions, diagnosis and management. Lancet 2000;356:1255-9.  Back to cited text no. 3  [PUBMED]  [FULLTEXT]  
4.Schaad UB, Wedgwood-Krucko J, Tschaeppeler H. Reversible ceftriaxone-associated biliary pseudolithiasis in children. Lancet 1988;2:1411-3.  Back to cited text no. 4  [PUBMED]    
5.Papadopoulou F, Efremidis S, Karyda S, Badouraki M, Karatza E, Panteliadis C, et al. Incidence of ceftriaxone-associated gallbladder pseudolithiasis. Acta Paediatr 1999;88:1352-5.  Back to cited text no. 5  [PUBMED]  [FULLTEXT]  
6.Acun C, Erdem LO, Sogut A, Erdem CZ, Tomac N, Gundogdu S. Ceftriaxone-induced biliary pseudolithiasis and urinary bladder sludge. Pediatr Int 2004;46:368-70.  Back to cited text no. 6  [PUBMED]  [FULLTEXT]  
7.Kirejczyk WM, Crowe HM, Mackay IM, Quintiliani R, Cronin EB. Disappearing "gallstones": Biliary pseudolithiasis complicating ceftriaxone therapy. AJR Am J Roentgenol 1992;159:329-30.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]  
8.Herek O, Pakdemirli E, Kocer N. Ceftriaxone-associated biliary pseudolithiasis in children. Eur Radiol 2001;11:902.  Back to cited text no. 8      



 
 
    Tables

  [Table 1], [Table 2]

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