5
REVIEW Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature Julian Booker*, Daniel Musher Cardiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA Accepted 7 February 2007 Available online 16 April 2007 KEYWORDS Endocarditis; Streptococcus pneumoniae; Pneumococcus; Dural sinus thrombosis; Cavernous sinus thrombosis Summary Streptococcus pneumoniae endocarditis is most commonly associated with pneu- monia. It is relatively uncommon disease but its severity makes it clinically relevant. We present a case and review of sinusitis complicated by both pneumococcal endocarditis and cavernous sinus thrombosis. Both endocarditis and dural sinus thrombosis are known complications of facial infections. To our knowledge, this is the first reported case of both S. pneumoniae endocarditis and dural sinus thrombosis complicating sinusitis. A case report and review of the literature is presented. ª 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved. Introduction Prior to the advent of widespread antibiotics, Streptococ- cus pneumoniae, or pneumococcus, was a relatively com- mon cause of bacterial endocarditis accounting for approximately 15% of all cases. 1 In contrast, at present, pneumococci account for <1e3% of cases of native valve endocarditis in adults. 2e9 Most cases occur in association with pneumonia. 2,10,11 We report a case of sphenoid sinus- itis leading to dural sinus thrombosis and ultimately pneu- mococcal endocarditis. Case presentation A 37-year-old man was hospitalized because of a four-day history of malaise, sinus discomfort, headache, and altered mentation. On admission he had an early systolic murmur consistent with mitral regurgitation, meningeal signs and left sixth nerve palsy. Lumbar puncture was not done because the prothrombin time was markedly prolonged. The patient developed rapidly progressive unilateral prop- tosis, visual disturbance, and became more lethargic. Soon thereafter, CT imaging of the head revealed sphenoid inflammation consistent with sinusitis (Fig. 1) along with evidence for thrombosis of the cavernous sinus (Fig. 2) extending to the left sigmoid sinus and down to the left jug- ular bulb. There were also several hypodense areas sugges- tive of septic embolization present with associated mass * Corresponding author. Tel.: þ1 713 433 1626. E-mail address: [email protected] (J. Booker). 0163-4453/$30 ª 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved. doi:10.1016/j.jinf.2007.02.011 www.elsevierhealth.com/journals/jinf Journal of Infection (2007) 55, 106e110

Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

Embed Size (px)

Citation preview

Page 1: Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

www.elsevierhealth.com/journals/jinf

Journal of Infection (2007) 55, 106e110

REVIEW

Sinusitis complicated by dural sinus thrombosisand Streptococcus pneumoniae endocarditis:A case report and review of the literature

Julian Booker*, Daniel Musher

Cardiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA

Accepted 7 February 2007Available online 16 April 2007

KEYWORDSEndocarditis;Streptococcuspneumoniae;Pneumococcus;Dural sinus thrombosis;Cavernous sinusthrombosis

Summary Streptococcus pneumoniae endocarditis is most commonly associated with pneu-monia. It is relatively uncommon disease but its severity makes it clinically relevant.

We present a case and review of sinusitis complicated by both pneumococcal endocarditisand cavernous sinus thrombosis.

Both endocarditis and dural sinus thrombosis are known complications of facial infections.To our knowledge, this is the first reported case of both S. pneumoniae endocarditis and duralsinus thrombosis complicating sinusitis. A case report and review of the literature is presented.ª 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved.

Introduction

Prior to the advent of widespread antibiotics, Streptococ-cus pneumoniae, or pneumococcus, was a relatively com-mon cause of bacterial endocarditis accounting forapproximately 15% of all cases.1 In contrast, at present,pneumococci account for <1e3% of cases of native valveendocarditis in adults.2e9 Most cases occur in associationwith pneumonia.2,10,11 We report a case of sphenoid sinus-itis leading to dural sinus thrombosis and ultimately pneu-mococcal endocarditis.

* Corresponding author. Tel.: þ1 713 433 1626.E-mail address: [email protected] (J. Booker).

0163-4453/$30 ª 2007 The British Infection Society. Published by Elsedoi:10.1016/j.jinf.2007.02.011

Case presentation

A 37-year-old man was hospitalized because of a four-dayhistory of malaise, sinus discomfort, headache, and alteredmentation. On admission he had an early systolic murmurconsistent with mitral regurgitation, meningeal signs andleft sixth nerve palsy. Lumbar puncture was not donebecause the prothrombin time was markedly prolonged.The patient developed rapidly progressive unilateral prop-tosis, visual disturbance, and became more lethargic. Soonthereafter, CT imaging of the head revealed sphenoidinflammation consistent with sinusitis (Fig. 1) along withevidence for thrombosis of the cavernous sinus (Fig. 2)extending to the left sigmoid sinus and down to the left jug-ular bulb. There were also several hypodense areas sugges-tive of septic embolization present with associated mass

vier Ltd. All rights reserved.

Page 2: Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

Sinusitis complicated by dural sinus thrombosis and S. pneumoniae endocarditis 107

effect and diffuse edema. Further CT imaging yielded noevidence of cardiopulmonary disease including pneumonia,but there was evidence for embolism to the kidneys. Atransthoracic echocardiogram revealed a large, mobile

Figure 1 Inflammatory mucosal changes (arrow) consistentwith sphenoid sinusitis.

Figure 2 Ophthalmic vein dilation and thrombosis (arrow)which is highly suggestive of cavernous sinus thrombosis.

mitral valve vegetation (Fig. 3) with severe regurgitation.There was no discernable involvement of the aortic valve.Prior to the initiation of antibiotics, four blood cultures weredrawn, all of which grew penicillin-susceptible S. pneumo-niae. The patient was evaluated for possible repair of themitral valve, but surgery was not done because of complexnon-medical issues. The patient received meningitis dosedceftriaxone for a total of six weeks with significant improve-ment and was later discharged.

Methods

A Pubmed search of the English literature from 1966 to thepresent and reference lists from previously reviewedarticles yielded 306 cases of pneumococcal endocarditis.When available, the following information was collected:patient demographics, risk factors, additional sites ofinfection, complications of the illness, echocardiographicfindings, treatment modalities and mortality.

Results

Including the present case, 307 cases of pneumococcalendocarditis from the antibiotic era were reviewed. Asnoted previously by other authors, the most frequent riskfactor was chronic alcoholism, which was seen in 32% ofpatients. Male to female showed a male predominance witha ratio of 2.8:1. The lung continues to be the most frequentportal of entry accounting for at least half of all casesthough head and neck sources of infection are not un-common. The aortic valve is the most frequently involvedvalve followed by the mitral valve (Table 1).

Heart failure and embolic phenomena are commoncomplications being present 45% and 32%, respectively.The rate of mortality was lower in individuals who receiveda combined medical and surgical approach to treatmentcompared to antibiotics alone. The outcomes for patientswith penicillin-resistant strains of pneumococcus weresimilar to those with penicillin-susceptible strains (Table 2).

Figure 3 Large anterior leaflet mitral valve vegetation.

Page 3: Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

108 J. Booker, D. Musher

Discussion

Pneumococcal endocarditis, though not as prevalent as itonce was, is not an infrequent occurrence. Less than 1% ofindividuals with documented pneumococcal bacteremiawill develop endocarditis, which correlates to approxi-mately 1e3 cases per one million inhabitants per year.12

Table 1 Demographics and clinical characteristics

GenderMale 173Female 61Male:female 2.8:1

Risk factors (n Z 241)Mean age 51Alcoholism 76 32%Diabetes 13 5%Malignancy 17 7%HIV 17 7%Asplenia 7 3%

Valvular abnormalities (n Z 236)Native valvular disease 47 20%Prosthetic valve 12 5%

Portal of entry (n Z 181)Lung 92 51%ENT 27 15%Skin 2 1%GU 1 <1%GI 1 <1%Unknown 58 32%

Clinical manifestations (n Z 210)Pneumonia 104 50%Meningitis 109 52%Peripheral stigmata 10 5%Duration of symptoms (days) 12

Table 2 Cardiac findings and clinical outcomes

Complications (n Z 254)CHF 113 45%Arterial emboli 81 32%Brain 20 8%Other 63 25%

Valves involved (n Z 231)Aortic 141 61%Mitral 81 35%Tricuspid 25 11%Pulmonary 2 <1%2 or more 27 12%

MortalityAntibiotics alone 76/145 52%Combined surgery and antibiotics 27/95 28%PCN susceptible 19/99 19%PCN resistant 8/33 24%

The mortality, however, remains high with rates as highas 60%.6,10,11

A number of risk factors have been associated withinvasive pneumococcal disease including alcoholism, im-mune suppression, chronic disease, extremes of age, andpneumococcal serotype.1,12e16 Human Immune DeficiencyVirus (HIV) is a known risk factor for invasive S. pneumoniaethough its role as a risk factor for endocarditis is lesswell defined.17e19 Alcoholism and valvular heart diseaseare the most oft noted risk factors for developing thedisease.3,20e23

When pneumococcus infects endocardium, the aorticvalve seems to be particularly susceptible6,7,20 and is in-volved 61% of the time in our review (Table 2). Though sero-types 1, 8, and 12 have been reported as occurring mostfrequently,3 it is suggested that any serotype is capable ofendocardial infection.12 To date, no specific virulence factorfor increased risk of endocarditis has been identified.12,24

Pneumococcal endocarditis typically evolves secondaryto infection of the respiratory tract.6,7 Pneumonia remainsthe most commonly predisposing disease process and likelythe inciting event in most cases. Much less frequently, caseshave followed documented infections in the sinuses, otitismedia, septic abortion and tooth extraction.6,10,26 Endocar-ditis caused by S. pneumoniae is often associated withpneumonia and suppurative meningitis. This clinical syn-drome was initially described by Heschl in 1862 and thenagain by Osler in 1881 and is referred to as Austrian syn-drome or Osler’s triad.

This syndrome, when present in an individual withalcoholism, is sometimes called Osler’s tetrad.23

Pneumococcal endocarditis most frequently presentsacutely and with brisk clinical decompensation. Pneumo-coccal infection of cardiac valves is aggressive and leads torapid valvular destruction and circulatory collapse fromheart failure. There also is a tendency for the developmentof large friable vegetations, which are prone to emboliza-tion.27 Data from France suggest that early valve rep-lacement may lead to less early death17 probably due tocorrection of hemodynamically unstable valvular abnormal-ities and fewer embolic events.

Historically, penicillin has been the treatment of choicefor endocarditis due to pneumococcus. Although nearly 40%of S. pneumoniae in the United States show some level ofresistance to penicillin,28,29 plasma levels of penicillin arewell above the minimum inhibitory concentration for mostof the treatment period,30 and experimental data suggeststerilization of valvular vegetations due to pneumococcuswith high dose penicillin alone.31 Currently there is no evi-dence to support the concern that the use of penicillin totreat pneumococcal endocarditis caused by penicillin-resistant pneumococcus leads to poorer outcomes thoughmany clinicians would defer to another antibiotic choice.

Despite advances in therapy over the past decades, themortality from pneumococcal endocarditis remains high,though we found the mortality to be lower than previouslyreported by Aronin. The mortality rate of individuals whoundergo medical therapy alone continues to be higher thanthose treated with a combined medicalesurgical approach(Table 2), likely to the high rate of acute valvular insuffi-ciency with cardiovascular collapse, and the high rate ofembolic phenomena. A selection bias also likely exists, in

Page 4: Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

Sinusitis complicated by dural sinus thrombosis and S. pneumoniae endocarditis 109

which only the better candidates are taken for surgery. Thedecreased mortality found in this review compared to priorfindings is due to improved survival documented in recentyears.

It is unclear how much, if any protection is conferredwith previous vaccination against S. pneumoniae. There isvery limited data on the rate of endocardial infection in in-dividuals who have received the vaccine.21 Vaccination has,however, decreased the total number of invasive pneumo-coccal infections32e35 and presumably indirectly decreasesthe overall incidence of pneumococcal endocarditis.

Dural sinus thrombosis, as seen in our patient, is a well-known and feared complication of sinusitis that has alsobecome increasingly rare during the antibiotic era. Thecavernous sinus is affected most frequently.36 Infectionsoriginating in the middle third of the face are the mostlikely sources for septic thrombosis of the cavernous sinusas they drain to the ophthalmic vein and ultimately to thecavernous sinus.36e38 The mainstay of therapy for duralsinus thrombosis is antibiotics with varying indications forsurgery for the different regions of thrombosis.36,39e41

To our knowledge, this is the first reported case ofpneumococcal sinusitis complicated by both dural sinusthrombosis and endocarditis.

References

1. Thayer WS. Bacterial or infective endocarditis; Gibsonlectures for 1930. Edinburgh Medical Journal 1931;38:237e

65 [307e34].2. Martinez E, Miro JM, Alimirante B, Aguado JM, Fernandez-

Viladrich P, Fernandez-Guerrero ML, et al. Effect of penicillinresistance of Streptococcus pneumoniae on the presentation,prognosis, and treatment of pneumococcal endocarditis inadults. Clin Infect Dis 2002;35:130e9.

3. Aronin SI, Mukherjee SK, West JC, Cooney EL. Review of pneu-mococcal endocarditis in adults in the penicillin era. CID 1998;1:165e71.

4. Bruyn GAW, Thompson J, Van Der Meer JWM. Pneumococcalendocarditis in adult patients. A report of five cases and reviewof the literature. Q J Med 1990;74:33e40.

5. Clark R, Carlisle JT, Valainis GT. Streptococcus pneumoniaeendocarditis presenting as an epidural abscess. Rev Infect Dis1989;11:338e40.

6. Sands M, Brown RB, Ryczak M, Hamilton W. Streptococcuspneumoniae endocarditis. South Med J 1987;80:780e2.

7. Powderly WG, Stanley Jr SL, Medoff G. Pneumococcal endocar-ditis: report of a series and review of the literature. Rev InfectDis 1986;8:786e91.

8. Bayliss R, Clarke C, Oakley CM, Somerville W, Whitfield AGW,Young SEJ. The microbiology and pathogenesis of infectiveendocarditis. Br Heart J 1983;50:513e9.

9. Staus AL, Hamburger M. Pneumococcal endocarditis in thepenicillin era. Arch Inten Med 1966;118:190e8.

10. Wolff M, Regnier B, Witchitz S, Gilbert C, Amoudry C, Vachon F.Pneumococcal endocarditis. Eur Heart J 1984;5(Suppl. C):77e80.

11. Ugolini V, Pacifico A, Smitherman TC, Mackowiak PA. Pneumo-coccal endocarditis update: analysis of 10 cases diagnosedbetween 1974 and 1984. Am Heart J 1986;112:813e9.

12. Kan B, Ries J, Henriques Normark J, Chang F-Y, Feldman C,Ko WC, et al. Endocarditis and pericarditis complicating pneu-mococcal bacteraemia, with special reference to the adhesiveabilities of pneumococci: results from a prospective study. ClinMicrobiol Infect 2006;12:338e44.

13. Burman LA, Norrby R, Trollfors B. Invasive pneumococcal infec-tions: incidence, predisposing factors, and prognosis. Rev In-fect Dis 1985;7:133e42.

14. Mufson MA, Kruss DM, Wasil RE, Metzger WI. Capsular types andoutcome of bacteremic pneumococcal disease in the antibioticera. Arch Intern Med 1974;134:505e10.

15. Filice GA, Darby CP, Fraser DW. Pneumococcal bacteremia inCharleston county, south Carolina. Am J Epidemiol 1980;112:828e35.

16. Ort S, Ryan JL, Barden G, d’Esopo N. Pneumococcal pneumoniain hospitalized patients: clinical and radiological presenta-tions. JAMA 1983;249:214e8.

17. Lefort A, Mainardi JL, Selton-Suty C, Casassus P, Guillevin L,Lortholary O. Streptococcus pneumoniae endocarditis inadults. A multicenter study in France in the era of penicillinresistance (1991e98). The Pneumococcal Endocarditis StudyGroup. Medicine (Baltimore) 2000;79:327e37.

18. Janoff EN, Breiman RF, Daley CL, Hopewell PC. Pneumococcaldisease during HIV infection. Epidemiologic, clinical, andimmunologic perspectives. Ann Intern Med 1992;117:314e24.

19. Nuorti JP, Butler JC, Gelling L, Kool JL, Reingold AL, Vugia DJ.Epidemiologic relation between HIV and invasive pneumococ-cal disease in San Francisco County, California. Ann InternMed 2000;132:182e90.

20. Gransden WR, Eykyn SJ, Phillips I. Pneumococcal bacteremia:325 episodes diagnosed at St Thomas’s hospital. BMJ 1985;290:505e8.

21. Finley JC, Davidson M, Parkinson AJ, Sullivan RW. Pneumo-coccal endocarditis in Alaska natives: a population-based ex-perience, 1978 through 1990. Arch Intern Med 1992;152:1641e5.

22. Buchbinder NA, Roberts WC. Left-sided valvular active infec-tive endocarditis: a study of forty-five necropsy patients. AmJ Med 1972;53:20e35.

23. Buchbinder NA, Roberts WC. Alcoholism: an important but un-emphasized factor predisposing to infective endocarditis. ArchIntern Med 1973;132:689e92.

24. Swiatlo E, Champlin FR, Holman SC, Wilson WW, Watt JM.Contribution of choline-binding proteins to cell surface pro-perties of Streptococcus pneumoniae. Infect Immun 2002;70:412e5.

26. Whitby S, Pallera A, Schaberg DR, Bronze MS. Infective endo-carditis caused by Streptococcus pneumoniae with high-levelresistance to penicillin and cephalosporin. Clin Infect Dis1996;23:1176e7.

27. Lord FT. Pneumococcus endocarditis. N Engl J Med 1932;207:767e8.

28. Thornsberry C, Sahm DF, Kelly LJ, Critchely IA, Jones ME,Evangelista AT, et al. Regional trends in antimicrobial resis-tance among clinical isolates of Streptococcus pneumoniae,Haemophilus influenzae, and Moraxella catarrhalis in theUnited States: results from the TRUST Surveillance Program,1999e2000. Clin Infect Dis 2002;34(Suppl. 1):S4.

29. Whitney CG, Farley MM, Hadler J, Harrison LH, Lexau C,Reingold A, et al. Increasing prevalence of multidrug-resistantStreptococcus pneumoniae in the United States. N Engl J Med2000;343:1917.

30. Musher DM, Bartlett JG, Doern GV. A fresh look at the definitionof susceptibility of Streptococcus pneumoniae to beta-lactamantibiotics. Arch Intern Med 2001;161:2538e44.

31. Fernandez Guerrero ML, Arbol F, Verdejo C, FernandezRoblas R, Soriano F. Treatment of experimental endocarditisdue to penicillin-resistant Streptococcus pneumoniae. Antimi-crob Agents Chemother 1994;38:1103e6.

32. Butler J, Breiman R, Campbell J, Lipman HB, Broome CV,Facklam RR. Pneumococcal polysaccharide vaccine efficacy:an evaluation of current recommendations. JAMA 1993;270:1826.

Page 5: Sinusitis complicated by dural sinus thrombosis and Streptococcus pneumoniae endocarditis: A case report and review of the literature

110 J. Booker, D. Musher

33. Shapiro ED, Bert AT, Austrian R, Schroeder D, Parcells V,Margolis A, et al. The protective efficacy of polyvalent pneu-mococcal polysaccharide vaccine. N Engl J Med 1991;325:1453.

34. Jackson LA, Neuzil KM, Yu O, Benson P, Barlow WE, Adams AL,et al. Effectiveness of pneumococcal polysaccharide vaccine inolder adults. N Engl J Med 2003;348:1747.

35. Dominguez A, Salleras L, Fedson DS, Izquierdo C, Ruiz L,Ciruela P, et al. Effectiveness of pneumococcal vaccinationfor elderly people in Catalonia, Spain: a caseecontrol study.Clin Infect Dis 2005;40:1250.

36. Southwick FS, Richardson Jr EP, Swartz MN. Septic thrombosisof the dural venous sinuses. Medicine (Baltimore) 1986;65:82.

37. Lew D, Southwick FS, Montgomery WW, Weber AL, Baker AS.Sphenoid sinusitis: a review of 30 cases. N Engl J Med 1983;309:1149.

38. Sadun F, Feldon SE, Weiss MH, Krieger MD. Septic cavernoussinus thrombosis following transsphenoidal craniotomy. Casereport. J Neurosurg 1996;85:949.

39. Seid AB, Sellars SL. The management of otogenic lateral sinusdisease at Groote Schuur Hospital. Laryngoscope 1973;83:397.

40. Singh BS. The management of lateral sinus thrombosis. J Lar-yngol Otol 1993;107:803.

41. Wong I, Kozak FK, Poskitt K, Ludemann JP, Harriman M. Pediat-ric lateral sinus thrombosis: retrospective case series and liter-ature review. J Otolaryngol 2005;34:79.