Hyperbilirubinemia as a Possible Predictor of Appendiceal Perforation in Acute Appendicitis: A Prospective Study

Sibabrata Kar, Tapan K Behera, Kumaramani Jena, Ashok Kumar Sahoo, Sibabrata Kar, Tapan K Behera, Kumaramani Jena, Ashok Kumar Sahoo

Abstract

Introduction: Acute appendicitis, a common abdominal surgical emergency, can mostly be diagnosed clinically by assessing the symptoms and physical findings but confirmation of the diagnosis solely depends upon the histopathological study of the resected appendix specimen, being supplemented by a few laboratory tests and ultrasonography (USG). In spite of all these available investigations, the diagnosis of acute appendicitis, because of its nebulous presentation and the variability of signs, remains a Herculean task for the surgeon.

Methods: This is a prospective study conducted on 125 patients diagnosed with acute appendicitis and posted for appendicectomy. Total serum bilirubin (TSB), and total leucocyte count (TLC) were done in all cases. USG of the abdomen was done in all the cases to confirm the diagnosis and to rule out other causes of acute abdomen. TLC more than 11 x 103 cells/µL and TSB more than 1.1 mg/dL were considered positive. They were operated on and their diagnoses were confirmed post-operatively by histopathological examination. Patients were subdivided according to histopathological findings into: normal appendix (n = 11), uncomplicated acute appendicitis (n = 86), gangrenous appendicitis (n = 10) and perforated appendix (n = 18). Laboratory results, operative findings, and histopathological findings were compiled, analyzed, and compared with reference values.

Results: Out of 125 patients, 114 (91.2%) were histologically positive for acute appendicitis, while 11 (8.8%) had normal histology. TLC was elevated in 95 (76 %) patients and it was normal in 30 (24%) cases. Among the patients with leucocytosis, only 90 (94.74%) had positive histology for acute appendicitis, while the remaining five (5.26%) had normal histology. Among the 30 patients who had normal TLC, 24 had positive histology for acute appendicitis, while the remaining six had normal histology. The specificity, sensitivity, positive predictive value (PPV), and negative predictive value (NPV) were 78.95%, 54.55%, 94.74%, and 20%respectively. Similarly, 67 patients (53.6%) had elevated TSB, while it was within normal limits in 58 (46.4%) patients. From the patients with hyperbilirubinemia, 65 (97.01%) had positive histology for acute appendicitis, while the remaining two (2.99%) had normal histology. Among 58 patients who had normal TSB, 49 had positive histology for acute appendicitis, while the rest nine had normal histology. The specificity, sensitivity, PPV, and NPV are 57.02%, 81.82%, 97.01%, and 15.52% respectively. However, when both TLC and TSB were compared as markers of appendicular perforation, the sensitivity, specificity, PPV, and NPV of total serum bilirubin were found to be 89.29% against 21.43%; 53.49% vs. 2.33%; 38.46% vs. 6.67% and 93.88% vs. 8.33% of total leukocyte counts respectively.

Conclusion: Elevated total serum bilirubin could be used as a better predictor of appendiceal perforation in acute appendicitis.

Keywords: acute appendicitis; histopathology; hyperbilirubinaemia; total leukocyte count; total serum bilirubin.

Conflict of interest statement

The authors have declared that no competing interests exist.

Copyright © 2022, Kar et al.

Figures

Figure 1. Distribution of patients as per…
Figure 1. Distribution of patients as per Histopathological report

References

    1. Appendicitis. Graffeo CS, Counselman FL. Emerg Med Clin North Am. 1996;14:653–671.
    1. A comparative study of pre-operative with operative diagnosis in acute abdomen. Chhetri RK, Shrestha ML. Kathmandu Univ Med J (KUMJ) 2005;3:107–110.
    1. Computer-aided diagnosis of acute abdominal pain. de Dombal FT, Leaper DJ, Staniland JR, McCann AP, Horrocks JC. Br Med J. 1972;2:9–13.
    1. Are some some appendectomies unnecessary? An analysis of 319 white appendices. Deutsch AA, Shani N, Reiss R. J R Coll Surg Edinb. 1983;28:35–40.
    1. Emergency room patients with abdominal pain unrelated to trauma: prospective analysis in a surgical university hospital. Simmen HP, Decurtins M, Rotzer A, Duff C, Brütsch HP, Largiadèr F. Hepatogastroenterology. 1991;38:279–282.
    1. Helical CT of appendicitis and diverticulitis. Rao PM, Rhea JT, Novelline RA. Radiol Clin North Am. 1999;37:895–910.
    1. Diagnosis of acute appendicitis. Grönroos JM, Grönroos P. Radiology. 2001;219:297–298.
    1. Leucocyte count and C-reactive protein in the diagnosis of acute appendicitis. Grönroos JM, Grönroos P. Br J Surg. 1999;86:501–504.
    1. A fertile-aged woman with right lower abdominal pain but unelevated leukocyte count and C-reactive protein. Acute appendicitis is very unlikely. Grönroos JM, Grönroos P. Langenbecks Arch Surg. 1999;384:437–440.
    1. Appendicitis at the millennium. Birnbaum BA, Wilson SR. Radiology. 2000;215:337–348.
    1. Acute appendicitis: high-resolution real-time US findings. Jeffrey RB Jr, Laing FC, Lewis FR. Radiology. 1987;163:11–14.
    1. A prospective study of ultrasonography in the diagnosis of appendicitis. Puylaert JB, Rutgers PH, Lalisang RI, de Vries BC, van der Werf SD, Dörr JP, Blok RA. N Engl J Med. 1987;317:666–669.
    1. Sonographic detection of the normal and abnormal appendix. Rioux M. AJR Am J Roentgenol. 1992;158:773–778.
    1. A practical score for the early diagnosis of acute appendicitis. Alvarado A. Ann Emerg Med. 1986;15:557–564.
    1. Evaluation of the modified Alvarado score in the diagnosis of acute appendicitis: a prospective study. Kalan M, Talbot D, Cunliffe WJ, Rich AJ. Ann R Coll Surg Engl. 1994;76:418–419.
    1. Modified Alvarado Scoring System as a diagnostic tool for acute appendicitis at Bugando Medical Centre, Mwanza, Tanzania. Kanumba ES, Mabula JB, Rambau P, Chalya PL. BMC Surg. 2011;11:4.
    1. Evaluation of hyperbilirubinemia in acute inflammation of appendix: a prospective study of 45 cases. Khan S. Kathmandu Univ Med J (KUMJ) 2006;4:281–289.
    1. Translocation of certain indigenous bacteria from the gastrointestinal tract to the mesenteric lymph nodes and other organs in a gnotobiotic mouse model. Berg RD, Garlington AW. Infect Immun. 1979;23:403–411.
    1. Frequency of portal and systemic bacteremia in acute appendicitis. Juric I, Primorac D, Zagar Z, et al. Pediatr Int. 2001;43:152–156.
    1. A bacteriologic study of human portal blood: implications regarding hepatic ischemia in man. Orloff MJ, Peskin GW, Ellis HL. Ann Surg. 1958;148:738–746.
    1. Tumor necrosis factor-alpha produces hepatocellular dysfunction despite normal cardiac output and hepatic microcirculation. Wang P, Ayala A, Ba ZF, Zhou M, Perrin MM, Chaudry IH. Am J Physiol. 1993;265:0–32.
    1. Hepatic extraction of indocyanine green is depressed early in sepsis despite increased hepatic blood flow and cardiac output. Wang P, Ba ZF, Chaudry IH. . Arch Surg. 1991;126:219–224.
    1. Mechanism of hepatocellular dysfunction during hyperdynamic sepsis. Wang P, Chaudry IH. Am J Physiol. 1996;270:0–38.
    1. Tumor necrosis factor-alpha decreases hepatocyte bile salt uptake and mediates endotoxin-induced cholestasis. Whiting JF, Green RM, Rosenbluth AB, Gollan JL. Hepatology. 1995;22:1273–1278.
    1. The diagnostic value of hyperbilirubinemia and total leucocyte count in the evaluation of acute appendicitis. Khan S. J Clin of Diagn Res. 2009;3:1647–1652.
    1. Hyperbilirubinemia as a predictor of gangrenous/perforated appendicitis: a prospective study. Chaudhary P, Kumar A, Saxena N, Biswal UC. Ann Gastroenterol. 2013;26:325–331.
    1. Preoperative diagnostic role of hyperbilirubinaemia as a marker of appendix perforation. Atahan K, Üreyen O, Aslan E, et al. J Int Med Res. 2011;39:609–618.
    1. The role of Bacteroides fragilis in the pathogenesis of acute appendicitis. Pieper R, Kager L, Weintraub A, Lindberg AA, Nord CE. Acta Chir Scand. 1982;148:39–44.
    1. Acute appendicitis and Bacteroides fragilis. Pieper R, Kager L, Lindberg AA, Nord CE. Scand J Infect Dis Suppl. 1979:92–97.
    1. Hepatocellular dysfunction occurs earlier than the onset of hyperdynamic circulation during sepsis. Wang P, Ba ZF, Chaudry IH. Shock. 1995;3:21–26.

Source: PubMed

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