Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-22T16:31:27.921Z Has data issue: false hasContentIssue false

Factors influencing bacteraemia in patients with isomerism and CHD: the effects of functional splenic status and antibiotic prophylaxis

Published online by Cambridge University Press:  29 September 2016

Rohit S. Loomba*
Affiliation:
Department of Pediatric Cardiology, Children’s Hospital of Wisconsin/Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America
Andrew N. Pelech
Affiliation:
Department of Pediatric Cardiology, Children’s Hospital of Wisconsin/Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America
Robert H. Anderson
Affiliation:
Institute of Genetic Medicine, Newcastle University, Newcastle Upon Tyne, United Kingdom
*
Correspondence to: R. S. Loomba, Department of Pediatric Cardiology, Children’s Hospital of Wisconsin/Medical College of Wisconsin, 9000 Wisconsin Avenue, Milwaukee, WI 53226, United States of America. Tel: 414 266 2000; Fax: 414 266 3855; E-mail: [email protected]

Abstract

Background

“Heterotaxy syndrome”, best segregated as isomerism, is characterised by laterality defects of the thoraco-abdominal organs, causing functional impairment. In particular, the spleen is frequently affected, increasing susceptibility to bacteraemia. This study explored factors that may increase the risk of bacteraemia in patients with isomerism.

Methods

We identified patients with CHD and isomerism. Review of outpatient, inpatient, and surgical records was conducted to collect data and determine trends in the cohort. A Cox regression analysis was conducted to determine factors influencing freedom from bacteraemia (Fig 1).

Results

We identified 83 patients with CHD and isomerism – 17 (20%) who had documented episodes of bacteraemia with a total of 21 episodes. A majority (86%) were nosocomial. The median age at the time of bacteraemia was 4 months. Although splenic anatomy did appear to influence the risk of bacteraemia in univariate analysis, this significance was lost with multivariate analysis. None of the other factors was significantly associated in either univariate or multivariate analysis.

Conclusion

Specific factors such as splenic anatomy, atrial appendage isomerism, and antibiotic prophylaxis status are not significantly associated with the risk of bacteraemia in patients with CHD and isomerism. Nosocomial infections represent a majority of bacteraemia in these patients.

Type
Original Articles
Copyright
© Cambridge University Press 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Loomba, RS, Hlavacek, AM, Spicer, DE, Anderson, RH. Isomerism or heterotaxy: which term leads to better understanding? Cardiol Young 2015; 25: 17.Google Scholar
2. Uemura, H, Ho, SY, Devine, WA, Anderson, RH. Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both. Am J Cardiol 1995; 76: 846849.Google Scholar
3. Jacobs, JP, Anderson, RH, Weinberg, PM, et al. The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy. Cardiol Young 2007; 17 (Suppl 2): 128.Google Scholar
4. Loomba, R, Shah, PH, Anderson, RH. Fetal magnetic resonance imaging of malformations associated with heterotaxy. Cureus 2015; 7: e269.Google Scholar
5. Loomba, RS, Chandrasekar, S, Shah, PH, Sanan, P. The developing role of fetal magnetic resonance imaging in the diagnosis of congenital cardiac anomalies: a systematic review. Ann Pediatr Cardiol 2011; 4: 172176.Google Scholar
6. Loomba, RS, Pelech, AN, Shah, PH, Anderson, RH. Determining bronchial morphology for the purposes of segregating so-called heterotaxy. Cardiol Young 2015; 26: 113.Google Scholar
7. Loomba, RS, Ahmed, MM, Spicer, DE, Backer, CL, Anderson, RH. Manifestations of bodily isomerism. Cardiovasc Pathol 2016; 25: 173180.Google Scholar
8. Loomba, RS, Shah, PH, Anderson, RH. Radiologic considerations in heterotaxy: the need for detailed anatomic evaluation. Cureus 2016; 8: 112.Google ScholarPubMed
9. Nagel, BH, Williams, H, Stewart, L, Paul, J, Stumper, O. Splenic state in surviving patients with visceral heterotaxy. Cardiol Young 2005; 15: 469473.Google Scholar
10. Yamamura, K, Joo, K, Ohga, S, et al. Thrombocytosis in asplenia syndrome with congenital heart disease: a previously unrecognized risk factor for thromboembolism. Int J Cardiol 2013; 167: 22592263.Google Scholar
11. Loomba, RS, Anderson, RH. Letter to the editor regarding “situs inversus with levocardia, infrahepatic interruption of the inferior vena cava, and azygos continuation: a case report”. Surg Radiol Anat 2015; 37: 12891290.CrossRefGoogle Scholar
12. Loomba, R. Thrombocytosis in the setting of isomerism and a functionally univentricular heart. Cureus 2015; 7: 110.Google Scholar
13. Koudieh, M, McKenzie, ED, Fraser, CD Jr. Outcome of Glenn anastomosis for heterotaxy syndrome with single ventricle. Asian Cardiovasc Thorac Ann 2006; 14: 235238.Google Scholar
14. Loomba, RS. Arterial desaturation due to pulmonary arteriovenous malformations after the Kawashima. Ann Pediatr Cardiol 2015; 9: 14.Google Scholar
15. Loomba, RS, Aggarwal, S, Arora, RR, Anderson, R. Bodily isomerism is an independent risk factor for pulmonary hypertension in adults with congenital heart disease. Ther Adv Respir Dis 2016; 10: 104199.Google Scholar
16. Loomba, RS, Willes, RJ, Kovach, JR, Anderson, RH. Chronic arrhythmias in the setting of heterotaxy: differences between right and left isomerism. Congenit Heart Dis 2015; 11: 718.Google Scholar
17. Loomba, RS, Aggarwal, S, Gupta, N, et al. Arrhythmias in adult congenital patients with bodily isomerism. Pediatr Cardiol 2015; 37: 12811287.Google Scholar
18. Bartz, PJ, Driscoll, DJ, Dearani, JA, et al. Early and late results of the modified fontan operation for heterotaxy syndrome 30 years of experience in 142 patients. J Am Coll Cardiol 2006; 48: 23012305.Google Scholar
19. Loomba, RS, Nijhawan, K, Anderson, R. Impact of era, type of isomerism, and ventricular morphology on survival in heterotaxy: implications for therapeutic management. World J Pediatr Congenit Heart Surg 2016; 7: 5462.Google Scholar
20. Wu, MH, Wang, JK, Lue, HC. Sudden death in patients with right isomerism (asplenism) after palliation. J Pediatr 2002; 140: 9396.CrossRefGoogle ScholarPubMed
21. Katcher, AL. Familial asplenia, other malformations, and sudden death. Pediatrics 1980; 65: 633635.Google Scholar
22. Sadiq, M, Stumper, O, De Giovanni, JV, et al. Management and outcome of infants and children with right atrial isomerism. Heart 1996; 75: 314319.Google Scholar
23. Kanthan, R, Moyana, T, Nyssen, J. Asplenia as a cause of sudden unexpected death in childhood. Am J Forensic Med Pathol 1999; 20: 5759.Google Scholar
24. Song, J, Kang, IS, Huh, J, et al. Interstage mortality for functional single ventricle with heterotaxy syndrome: a retrospective study of the clinical experience of a single tertiary center. J Cardiothorac Surg 2013; 8: 93.Google Scholar
25. Gentles, TL, Mayer, JE Jr, Gauvreau, K, et al. Fontan operation in five hundred consecutive patients: factors influencing early and late outcome. J Thorac Cardiovasc Surg 1997; 114: 376391.Google Scholar
26. Knott-Craig, CJ, Danielson, GK, Schaff, HV, Puga, FJ, Weaver, AL, Driscoll, DD. The modified Fontan operation. An analysis of risk factors for early postoperative death or takedown in 702 consecutive patients from one institution. J Thorac Cardiovasc Surg 1995; 109: 12371243.Google Scholar
27. Humes, RA, Feldt, RH, Porter, CJ, Julsrud, PR, Puga, FJ, Danielson, GK. The modified Fontan operation for asplenia and polysplenia syndromes. J Thorac Cardiovasc Surg 1988; 96: 212218.Google Scholar
28. Rodin, AE, Sloane, JA, Nghiem, QX. Polysplenia with severe congenital heart disease and Howell-Jolly bodies. Am J Clin Pathol 1972; 58: 127134.Google Scholar
29. Barker, GM, O’Brien, SM, Welke, KF, et al. Major infection after pediatric cardiac surgery: a risk estimation model. Ann Thorac Surg 2010; 89: 843850.Google Scholar
30. Waldman, JD, Rosenthal, A, Smith, AL, Shurin, S, Nadas, AS. Sepsis and congenital asplenia. J Pediatr 1977; 90: 555559.CrossRefGoogle ScholarPubMed
31. Prendiville, TW, Barton, LL, Thompson, WR, Fink, DL, Holmes, KW. Heterotaxy syndrome: defining contemporary disease trends. Pediatr Cardiol 2010; 31: 10521058.Google Scholar
32. Chiu, SN, Shao, PL, Wang, JK, et al. Severe bacterial infection in patients with heterotaxy syndrome. J Pediatr 2014; 164: 99104; e101.Google Scholar
33. Bisharat, N, Omari, H, Lavi, I, Raz, R. Risk of infection and death among post-splenectomy patients. J Infect 2001; 43: 182186.Google Scholar
34. Hansen, K, Singer, DB. Asplenic-hyposplenic overwhelming sepsis: postsplenectomy sepsis revisited. Pediatr Dev Pathol 2001; 4: 105121.Google Scholar
35. Lynch, AM, Kapila, R. Overwhelming postsplenectomy infection. Infect Dis Clin North Am 1996; 10: 693707.CrossRefGoogle ScholarPubMed
36. Singer, DB. Postsplenectomy sepsis. Perspect Pediatr Pathol 1973; 1: 285311.Google Scholar
37. Holdsworth, RJ, Irving, AD, Cuschieri, A. Postsplenectomy sepsis and its mortality rate: actual versus perceived risks. Br J Surg 1991; 78: 10311038.Google Scholar
38. Brigden, ML, Pattullo, AL. Prevention and management of overwhelming postsplenectomy infection – an update. Crit Care Med 1999; 27: 836842.Google Scholar
39. Gaston, MH, Verter, JI, Woods, G, et al. Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. New Engl J Med 1986; 314: 15931599.CrossRefGoogle ScholarPubMed
40. Falletta, JM, Woods, GM, Verter, JI, et al. Discontinuing penicillin prophylaxis in children with sickle cell anemia. Prophylactic Penicillin Study II. J Pediatr 1995; 127: 685690.Google Scholar
41. Classen, DC, Evans, RS, Pestotnik, SL, Horn, SD, Menlove, RL, Burke, JP. The timing of prophylactic administration of antibiotics and the risk of surgical-wound infection. New Engl J Med 1992; 326: 281286.Google Scholar
42. Siegel, JD, McCracken, GH Jr, Threlkeld, N, Milvenan, B, Rosenfeld, CR. Single-dose penicillin prophylaxis against neonatal group B streptococcal infections. A controlled trial in 18738 newborn infants. New Engl J Med 1980; 303: 769775.Google Scholar
43. Crosby, WH. Hyposplenism: an inquiry into normal functions of the spleen. Annu Rev Med 1963; 14: 349370.Google Scholar
44. McCarthy, CF, Fraser, ID, Evans, KT, Read, AE. Lymphoreticular dysfunction in idiopathic steatorrhoea. Gut 1966; 7: 140148.Google Scholar
45. Harrod, VL, Howard, TA, Zimmerman, SA, Dertinger, SD, Ware, RE. Quantitative analysis of Howell-Jolly bodies in children with sickle cell disease. Exp Hematol 2007; 35: 179183.Google Scholar
46. Corazza, GR, Ginaldi, L, Zoli, G, et al. Howell-Jolly body counting as a measure of splenic function. A reassessment. Clin Lab Haematol 1990; 12: 269275.Google Scholar
47. Combs, LS, Gupta, S, Mehta, A. Evaluation of spleen in children with heterotaxia and congenital heart disease. Tennessee medicine. J Tenn Med Assoc 2004; 97: 161163.Google Scholar
48. Committee on Infectious Diseases American Academy of Pediatrics. Red Book: 2006 Report of the Committee on Infectious Diseases. Committee on Infectious Diseases American Academy of Pediatrics, Philadephia, Pennsylvania, 2006.Google Scholar
49. Chiu, SN, Shao, PL, Wang, JK, et al. Low immunoglobulin M memory B-cell percentage in patients with heterotaxy syndrome correlates with the risk of severe bacterial infection. Pediatr Res 2015; 70: 271277.Google Scholar