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Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019 25
INTRODUCTION
D
espite advances in modern diagnostic and treatment
strategies, infective endocarditis (IE) still carries a
substantial risk of complications and mortality.[1]
The prevalence of isolated tricuspid valve IE is estimated at
2.5–3.1%[2]
of all IE cases.
The risk factors for bacterial colonization as a source of
bacteremia for tricuspid valve endocarditis are intravenous
drug abusers, patients with implantable cardiac devices,
indwelling catheters, or congenital heart disease.[3]
A rare
cause of tricuspid valve IE, especially in grown-up age,
is cerebrospinal fluid (CSF) shunt-associated infections.
Nowadays, these cases are rarely described in literature.
Ventricular CSF shunts are commonly used in pediatric
neurosurgery for the treatment of hydrocephalus of
various etiologies. Most commonly performed are the
shunting procedures including ventriculoperitoneal (VP),
ventriculopleural, or ventriculoatrial (VA) shunt; endoscopic
third ventriculostomy implies surgical creation of an opening
in the floor of the third ventricle to enable drainage of CSF
into the cistern.[4]
In this case report, we describe a rare case of distal VA
catheter infection and catheter-related tricuspid valve IE.
Infective Endocarditis as a Complication of
Ventriculoatrial Shunting for Hydrocephalus Treatment
Maja Stefanović1,2
, Aleksandra Milovančev2
, Ilija Srdanović1,2
, Aleksandra Vulin2,3
,
Aleksandra Ilić2,3
, Lazar Velicki4,5
, Snežana Tadić2,3
, Snežana Bjelić1,2
, Tatjana Miljković2,3
1
Department of Emergency Medicine, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 2
Department
of Cardiology, Institute of Cardiovascular Diseases of Vojvodina, Sremska Kamenica, Serbia, 3
Department of
Internal Medicine, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 4
Department of Surgery,
Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 5
Department of Cardiac Surgery, Institute of
Cardiovascular Diseases of Vojvodina, Sremska Kamenica, Serbia
ABSTRACT
Our aim is to present a rare cause of tricuspid valve infective endocarditis (IE) in grown-up age due to cerebrospinal fluid shunt-
associated infection.A32-year-old woman, with a history of hydrocephalus that was treated with ventriculoperitoneal (VP) shunt
at the age of 4, was admitted to a hospital due to fever. The VP shunt was replaced several times due to dysfunction and replaced
with ventriculoatrial (VA) shunt 3 months before admission. Transesophageal echocardiogram revealed two separate VAcatheters
in the right atrium, with two floating echo formations, one attached to the tip of one catheter and the other to the anterior leaflet
of tricuspid valve. Blood cultures grew methicillin-susceptible Staphylococcus aureus. Computed tomography scan showed
bilateral pneumonia. The patient was treated with antibiotics followed by partial extraction of the VA shunt. After 8 weeks,
the patient was discharged, without signs of infection. Two months later, she was readmitted due to fever, echocardiographic
signs of catheter infection, and septic pulmonary embolization. Complete extraction of VA catheter was done and treatment was
continued with antibiotics with complete recovery. Early diagnosis and optimal management that combines both conventional
and surgical approaches is crucial for reducing the high embolic risk, risk of complications, and mortality risk.
Key words: Endocarditis, tricuspid valve, ventriculoatrial shunt
CASE REPORT
Address for correspondence:
Maja Stefanović, Department of Emergency Medicine, Faculty of Medicine, University of Novi Sad, 21 000 Novi Sad,
Serbia. Phone: +381638253766. E-mail: maja.stefanovic@mf.uns.ac.rs
https://doi.org/10.33309/2639-8265.020105 www.asclepiusopen.com
© 2019 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
Stefanović, et al.: Endocarditis as a complication of a ventriculo-atrial shunt
26 Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019
CASE REPORT
A32-year-old woman, with a history of innate hydrocephalus,
was admitted to a regional hospital due to fever, tachypnea,
and tachycardia. She complained of malaise, poor appetite,
cough, and pain in the lower back; the symptoms appeared a
week before admission.
Hydrocephalus developed as a result of aqueductal stenosis
and was treated with the right-sided VP shunt at the age of 4.
Due to malfunction, the VP shunt was subsequently replaced
for several times. VA shunt was inserted 3 months before
hospital admission and appeared to be functioning well.
Physical examination on admission revealed a body
temperature of 39.2°C, heart rate of 105 beats/min, respiratory
rate 22/min, and blood pressure of 110/60 mmHg. There were
no signs of meningeal irritation.
Chest X-ray showed bilateral pneumonia. Computed
tomography (CT) scan identified right-sided sacroiliitis
and confirmed bilateral pneumonia. Transthoracic
echocardiography (TTE) showed VA catheter tip in the right
atrium, with no pathological changes on the valves or the
catheter. Repeat blood cultures grew methicillin-susceptible
Staphylococcus aureus (MSSA) sensitive to vancomycin. The
patient was referred to tertiary hospital and further diagnostic
and treatment. Transesophageal echocardiography (TOE)
showed two separate VA catheters in the right atrium, with two
floating echo formations, one attached to the tip of one catheter
[Figure 1a] and the other to the anterior leaflet of the tricuspid
valve, associated with mild tricuspid regurgitation [Figure 1b].
Thoracic CT scan confirmed the existence of two twisted VA
catheters, right and left sided, in the right atrium.
The patient was treated with antibiotics, according to
antibiogram for MSSA. Repeated blood cultures remained
sterile. After neurosurgical consultation, she continued the
treatment at the clinic for neurosurgery, where a partial
extractionoftheVAshuntandplacementofnewVPshuntwere
performed. Due to malfunction, in the same hospitalization,
VP shunt was removed and replaced with ventriculopleural
shunt.The removedVAshunt was microbiologically negative.
The further treatment was complicated with the development
of the shunt-related nephritis. After 8 weeks of treatment,
the patient was discharged in good general condition, with
no signs of infection. Two months later, she was readmitted
to hospital due to fever. Laboratory investigations revealed
anemia with hemoglobin of 74 g/l, leukocytosis with white
blood cells of 16, 5 × 109
/l, and raised C-reactive protein of
231 mg/l. Repeat blood culture grew methicillin-susceptible
S. aureus (MSSA) sensitive to vancomycin. TTE as well
as TOE showed a VA catheter within the right atrium with
echogenic structure (1.3 cm × 0.7 cm) at the tip of the catheter.
There was no vegetation on the tricuspid valve.
Thoracic CT scan confirmed the existence of VA catheter in
the right atrium and identified the presence of inflammatory
changes in both lungs that were complement to the septic
emboli, suspected right-sided lung abscesses and bilateral
pleural effusions. Endocarditis team reached a decision that
complete extraction of VAcatheter was warranted. Extraction
was performed through the internal jugular vein access by
a vascular surgeon. The intervention was performed without
complications. TTE was repeated following the procedure,
and there were no remaining catheter and no signs of IE.
Treatment with vancomycin was continued for 2 weeks after
this shunt removal, and repeated blood cultures remained
sterile. The patient was discharged in good general condition
with no signs of infection.
DISCUSSION
We present herein a rare case of tricuspid valve endocarditis
caused by VA shunt infection in adulthood. In the follow-up,
the patient was readmitted due to relapse of infection with
same microorganism complicated with shunt nephritis. Early
diagnostics and multidisciplinary treatment that combined
surgery and conventional antibiotic treatment led to complete
recovery.
VA shunt was one of the oldest solutions for hydrocephalus
that becomes standard treatment since 1952.[5]
Over
the subsequent years, this promising intervention led to
remarkable concerns with the recognition of various range of
severe complications related to[6]
catheter dysfunction such
as shunt infections, valve obstructions, catheter migrations,
Figure 1: Transesophageal echocardiography: (a) mid-
esophageal aortic valve short axis view 37°. Arrow points to
the floating echo formation connected to the tip of catheter.
AV: Aortic valve, RA: Right atrium. (b) Mid-esophageal four-
chamber view 0°. Arrow points to the floating echo formation
attached to the anterior leaflet of tricuspid valve. LV: Left
ventricle, RV: Right ventricle, LA: Left atrium
b
a
Stefanović, et al.: Endocarditis as a complication of a ventriculo-atrial shunt
Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019 27
shunt disconnections, malposition, or any combination
of these reasons. However, infections are one of the most
common complications of ventricular CSF shunts. Reports
on infections incidence are variable and varied from 0.3%
to 26%[7]
with a mortality rate ranging from 1.5% to 22%.
Shunt removal with internal antibiotic treatment (usually
with external ventricular drainage) carries the highest shunt
infection cure rate and lowest mortality rate.[8]
Today, VP shunts are the most preferred method of the
treatment of hydrocephalus, but there is a notable patient
population where VAshunt is needed.[6]
Follow-up of patients
with VA shunts is currently poorly defined. Consciousness
of complications of CSF shunts such as infection and IE
and long-term clinical and echocardiographic follow-up
in patients with VA shunts is necessary to prevent severe
complications in these patients.
CONCLUSION
This is a rare case of VA shunt infection complicated
by tricuspid valve IE uncommonly seen in adulthood in
nowadays. Early diagnosis and optimal management that
combinesbothconventionalandsurgicalapproachesiscrucial
for reducing the high embolic risk, risk of complications, and
mortality risk.
DECLARATIONS
Patient’s approval for publishing data and this case report.
We wish to confirm that there are no known conflicts of
interest associated with this publication and there has been
no significant financial support for this work that could have
influenced its outcome.
Maja Stefanović contribution to manuscript was study design,
analysis, interpretation of data, and writing the manuscript.
Ilija Srdanović critical revision of paper. Lazar Velicki
acquisition and collection of data. Snežana Tadić analysis
and interpretation of data. Aleksandra Ilić critical revision
of paper. Aleksandra Milovančev writing the manuscript.
Tatjana Miljković analysis and interpretation of data. Snežana
Bjelić interpretation of data.
REFERENCES
1.	 Hoen B, Duval X. Clinical practice. Infective endocarditis. N
Engl J Med 2013;368:1425-33.
2.	 Heydari AA, Safari H, Sarvghad MR. Isolated tricuspid valve
endocarditis. Int J Infect Dis 2009;13:e109-11.
3.	 D’AgostinoD,BottalicoL,SantacroceL.Infectiveendocarditis:
What is changed in epidemiology and prophylaxis. Acta Med
Mediterr 2012;28:311-9.
4.	 Hamid R, Kawsar S. Case report of a V-P shunt dependent child
withshuntdisconnectionandinfectionwithextended- spectrum
β-lactamase-producing Klebsiella pneumoniae (ESBL-KP).
Pediatr Infect Dis 2016;1:18.
5.	 Nulsen FE, Spitz EB. Treatment of hydrocephalus by
direct shunt from ventricle to jugular vain. Surg Forum
1951;2:399-403.
6.	 Vernet O, Rilliet B. Late complications of ventriculoatrial or
ventriculoperitoneal shunts. Lancet 2001;358:1569-70.
7.	 Ram Y, Tina QT. Infections related to prosthetic or artificial
devices. In: Cherry J, Demmler-Harrison G, Kaplan S,
William J. Steinbach MD, Peter J. Feigin and Cherry’s
Textbook of Pediatric Infectious Diseases. 7th
ed. Philadelphia,
PA: Elsevier-Saunders; 2014. p. 1029-30.
8.	 Schreffler RT, Schreffler AJ, Wittler RR. Treatment of
cerebrospinal fluid shunt infections: A decision analysis.
Pediatr Infect Dis J 2002;21:632-6.
How to cite this article: Stefanović M, Milovančev A,
Srdanović I, Vulin A, Ilić A, Velicki L, Tadić S, Bjelić S,
Miljković T. Infective Endocarditis as a Complication of
Ventriculoatrial Shunting for Hydrocephalus Treatment.
J Clin Cardiol Diagn 2019;2(1):25-27.

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Infective Endocarditis as a Complication of Ventriculoatrial Shunting for Hydrocephalus Treatment

  • 1. Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019 25 INTRODUCTION D espite advances in modern diagnostic and treatment strategies, infective endocarditis (IE) still carries a substantial risk of complications and mortality.[1] The prevalence of isolated tricuspid valve IE is estimated at 2.5–3.1%[2] of all IE cases. The risk factors for bacterial colonization as a source of bacteremia for tricuspid valve endocarditis are intravenous drug abusers, patients with implantable cardiac devices, indwelling catheters, or congenital heart disease.[3] A rare cause of tricuspid valve IE, especially in grown-up age, is cerebrospinal fluid (CSF) shunt-associated infections. Nowadays, these cases are rarely described in literature. Ventricular CSF shunts are commonly used in pediatric neurosurgery for the treatment of hydrocephalus of various etiologies. Most commonly performed are the shunting procedures including ventriculoperitoneal (VP), ventriculopleural, or ventriculoatrial (VA) shunt; endoscopic third ventriculostomy implies surgical creation of an opening in the floor of the third ventricle to enable drainage of CSF into the cistern.[4] In this case report, we describe a rare case of distal VA catheter infection and catheter-related tricuspid valve IE. Infective Endocarditis as a Complication of Ventriculoatrial Shunting for Hydrocephalus Treatment Maja Stefanović1,2 , Aleksandra Milovančev2 , Ilija Srdanović1,2 , Aleksandra Vulin2,3 , Aleksandra Ilić2,3 , Lazar Velicki4,5 , Snežana Tadić2,3 , Snežana Bjelić1,2 , Tatjana Miljković2,3 1 Department of Emergency Medicine, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 2 Department of Cardiology, Institute of Cardiovascular Diseases of Vojvodina, Sremska Kamenica, Serbia, 3 Department of Internal Medicine, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 4 Department of Surgery, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia, 5 Department of Cardiac Surgery, Institute of Cardiovascular Diseases of Vojvodina, Sremska Kamenica, Serbia ABSTRACT Our aim is to present a rare cause of tricuspid valve infective endocarditis (IE) in grown-up age due to cerebrospinal fluid shunt- associated infection.A32-year-old woman, with a history of hydrocephalus that was treated with ventriculoperitoneal (VP) shunt at the age of 4, was admitted to a hospital due to fever. The VP shunt was replaced several times due to dysfunction and replaced with ventriculoatrial (VA) shunt 3 months before admission. Transesophageal echocardiogram revealed two separate VAcatheters in the right atrium, with two floating echo formations, one attached to the tip of one catheter and the other to the anterior leaflet of tricuspid valve. Blood cultures grew methicillin-susceptible Staphylococcus aureus. Computed tomography scan showed bilateral pneumonia. The patient was treated with antibiotics followed by partial extraction of the VA shunt. After 8 weeks, the patient was discharged, without signs of infection. Two months later, she was readmitted due to fever, echocardiographic signs of catheter infection, and septic pulmonary embolization. Complete extraction of VA catheter was done and treatment was continued with antibiotics with complete recovery. Early diagnosis and optimal management that combines both conventional and surgical approaches is crucial for reducing the high embolic risk, risk of complications, and mortality risk. Key words: Endocarditis, tricuspid valve, ventriculoatrial shunt CASE REPORT Address for correspondence: Maja Stefanović, Department of Emergency Medicine, Faculty of Medicine, University of Novi Sad, 21 000 Novi Sad, Serbia. Phone: +381638253766. E-mail: maja.stefanovic@mf.uns.ac.rs https://doi.org/10.33309/2639-8265.020105 www.asclepiusopen.com © 2019 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
  • 2. Stefanović, et al.: Endocarditis as a complication of a ventriculo-atrial shunt 26 Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019 CASE REPORT A32-year-old woman, with a history of innate hydrocephalus, was admitted to a regional hospital due to fever, tachypnea, and tachycardia. She complained of malaise, poor appetite, cough, and pain in the lower back; the symptoms appeared a week before admission. Hydrocephalus developed as a result of aqueductal stenosis and was treated with the right-sided VP shunt at the age of 4. Due to malfunction, the VP shunt was subsequently replaced for several times. VA shunt was inserted 3 months before hospital admission and appeared to be functioning well. Physical examination on admission revealed a body temperature of 39.2°C, heart rate of 105 beats/min, respiratory rate 22/min, and blood pressure of 110/60 mmHg. There were no signs of meningeal irritation. Chest X-ray showed bilateral pneumonia. Computed tomography (CT) scan identified right-sided sacroiliitis and confirmed bilateral pneumonia. Transthoracic echocardiography (TTE) showed VA catheter tip in the right atrium, with no pathological changes on the valves or the catheter. Repeat blood cultures grew methicillin-susceptible Staphylococcus aureus (MSSA) sensitive to vancomycin. The patient was referred to tertiary hospital and further diagnostic and treatment. Transesophageal echocardiography (TOE) showed two separate VA catheters in the right atrium, with two floating echo formations, one attached to the tip of one catheter [Figure 1a] and the other to the anterior leaflet of the tricuspid valve, associated with mild tricuspid regurgitation [Figure 1b]. Thoracic CT scan confirmed the existence of two twisted VA catheters, right and left sided, in the right atrium. The patient was treated with antibiotics, according to antibiogram for MSSA. Repeated blood cultures remained sterile. After neurosurgical consultation, she continued the treatment at the clinic for neurosurgery, where a partial extractionoftheVAshuntandplacementofnewVPshuntwere performed. Due to malfunction, in the same hospitalization, VP shunt was removed and replaced with ventriculopleural shunt.The removedVAshunt was microbiologically negative. The further treatment was complicated with the development of the shunt-related nephritis. After 8 weeks of treatment, the patient was discharged in good general condition, with no signs of infection. Two months later, she was readmitted to hospital due to fever. Laboratory investigations revealed anemia with hemoglobin of 74 g/l, leukocytosis with white blood cells of 16, 5 × 109 /l, and raised C-reactive protein of 231 mg/l. Repeat blood culture grew methicillin-susceptible S. aureus (MSSA) sensitive to vancomycin. TTE as well as TOE showed a VA catheter within the right atrium with echogenic structure (1.3 cm × 0.7 cm) at the tip of the catheter. There was no vegetation on the tricuspid valve. Thoracic CT scan confirmed the existence of VA catheter in the right atrium and identified the presence of inflammatory changes in both lungs that were complement to the septic emboli, suspected right-sided lung abscesses and bilateral pleural effusions. Endocarditis team reached a decision that complete extraction of VAcatheter was warranted. Extraction was performed through the internal jugular vein access by a vascular surgeon. The intervention was performed without complications. TTE was repeated following the procedure, and there were no remaining catheter and no signs of IE. Treatment with vancomycin was continued for 2 weeks after this shunt removal, and repeated blood cultures remained sterile. The patient was discharged in good general condition with no signs of infection. DISCUSSION We present herein a rare case of tricuspid valve endocarditis caused by VA shunt infection in adulthood. In the follow-up, the patient was readmitted due to relapse of infection with same microorganism complicated with shunt nephritis. Early diagnostics and multidisciplinary treatment that combined surgery and conventional antibiotic treatment led to complete recovery. VA shunt was one of the oldest solutions for hydrocephalus that becomes standard treatment since 1952.[5] Over the subsequent years, this promising intervention led to remarkable concerns with the recognition of various range of severe complications related to[6] catheter dysfunction such as shunt infections, valve obstructions, catheter migrations, Figure 1: Transesophageal echocardiography: (a) mid- esophageal aortic valve short axis view 37°. Arrow points to the floating echo formation connected to the tip of catheter. AV: Aortic valve, RA: Right atrium. (b) Mid-esophageal four- chamber view 0°. Arrow points to the floating echo formation attached to the anterior leaflet of tricuspid valve. LV: Left ventricle, RV: Right ventricle, LA: Left atrium b a
  • 3. Stefanović, et al.: Endocarditis as a complication of a ventriculo-atrial shunt Journal of Clinical Cardiology and Diagnostics  •  Vol 2  •  Issue 1  •  2019 27 shunt disconnections, malposition, or any combination of these reasons. However, infections are one of the most common complications of ventricular CSF shunts. Reports on infections incidence are variable and varied from 0.3% to 26%[7] with a mortality rate ranging from 1.5% to 22%. Shunt removal with internal antibiotic treatment (usually with external ventricular drainage) carries the highest shunt infection cure rate and lowest mortality rate.[8] Today, VP shunts are the most preferred method of the treatment of hydrocephalus, but there is a notable patient population where VAshunt is needed.[6] Follow-up of patients with VA shunts is currently poorly defined. Consciousness of complications of CSF shunts such as infection and IE and long-term clinical and echocardiographic follow-up in patients with VA shunts is necessary to prevent severe complications in these patients. CONCLUSION This is a rare case of VA shunt infection complicated by tricuspid valve IE uncommonly seen in adulthood in nowadays. Early diagnosis and optimal management that combinesbothconventionalandsurgicalapproachesiscrucial for reducing the high embolic risk, risk of complications, and mortality risk. DECLARATIONS Patient’s approval for publishing data and this case report. We wish to confirm that there are no known conflicts of interest associated with this publication and there has been no significant financial support for this work that could have influenced its outcome. Maja Stefanović contribution to manuscript was study design, analysis, interpretation of data, and writing the manuscript. Ilija Srdanović critical revision of paper. Lazar Velicki acquisition and collection of data. Snežana Tadić analysis and interpretation of data. Aleksandra Ilić critical revision of paper. Aleksandra Milovančev writing the manuscript. Tatjana Miljković analysis and interpretation of data. Snežana Bjelić interpretation of data. REFERENCES 1. Hoen B, Duval X. Clinical practice. Infective endocarditis. N Engl J Med 2013;368:1425-33. 2. Heydari AA, Safari H, Sarvghad MR. Isolated tricuspid valve endocarditis. Int J Infect Dis 2009;13:e109-11. 3. D’AgostinoD,BottalicoL,SantacroceL.Infectiveendocarditis: What is changed in epidemiology and prophylaxis. Acta Med Mediterr 2012;28:311-9. 4. Hamid R, Kawsar S. Case report of a V-P shunt dependent child withshuntdisconnectionandinfectionwithextended- spectrum β-lactamase-producing Klebsiella pneumoniae (ESBL-KP). Pediatr Infect Dis 2016;1:18. 5. Nulsen FE, Spitz EB. Treatment of hydrocephalus by direct shunt from ventricle to jugular vain. Surg Forum 1951;2:399-403. 6. Vernet O, Rilliet B. Late complications of ventriculoatrial or ventriculoperitoneal shunts. Lancet 2001;358:1569-70. 7. Ram Y, Tina QT. Infections related to prosthetic or artificial devices. In: Cherry J, Demmler-Harrison G, Kaplan S, William J. Steinbach MD, Peter J. Feigin and Cherry’s Textbook of Pediatric Infectious Diseases. 7th ed. Philadelphia, PA: Elsevier-Saunders; 2014. p. 1029-30. 8. Schreffler RT, Schreffler AJ, Wittler RR. Treatment of cerebrospinal fluid shunt infections: A decision analysis. Pediatr Infect Dis J 2002;21:632-6. How to cite this article: Stefanović M, Milovančev A, Srdanović I, Vulin A, Ilić A, Velicki L, Tadić S, Bjelić S, Miljković T. Infective Endocarditis as a Complication of Ventriculoatrial Shunting for Hydrocephalus Treatment. J Clin Cardiol Diagn 2019;2(1):25-27.