Literature DB >> 36010333

Refractory Salmonella Prosthetic Valve Endocarditis Complicated by Splenic Infarction and Aortic Pseudoaneurysm in a Patient with Double Prosthetic Valves: A Case Report.

Moustafa S Alhamadh1,2, Rakan B Alanazi1,2, Thamer Saad Alhowaish1,2, Abdulrahman Yousef Alhabeeb1,2, Sultan T Algarni1,2, Osama Mohaamad Wadaan1,2, Ihab Suliman1,2,3, Mohammed Ghormalla Al-Ghamdi1,2,3.   

Abstract

Endocarditis is an extremely rare complication of Salmonellosis with an incidence of 0.2-0.4%. It is a destructive and invasive infection that follows a highly complicated course and carries a high mortality rate that exceeds 45%. Multiple predisposing factors for Salmonella endocarditis have been described in the literature, including human immunodeficiency virus infection, congenital heart diseases, and the presence of a prosthetic valve. Herein, we report a case of Salmonella prosthetic valve endocarditis complicated by splenic infarction and aortic pseudoaneurysm presenting as a month-long history of fluctuating fever, chills, and rigors, accompanied by occasional cough and shortness of breath in a 55-year-old female with aortic and mitral valves replacement and multiple comorbidities. She was diagnosed by multiple radiographic studies and successfully treated with the Commando procedure and a long course of IV antibiotics.

Entities:  

Keywords:  Commando procedure; Salmonella endocarditis; Salmonellosis; aortic pseudoaneurysm; prosthetic valve endocarditis; splenic infarction

Year:  2022        PMID: 36010333      PMCID: PMC9407200          DOI: 10.3390/diagnostics12081982

Source DB:  PubMed          Journal:  Diagnostics (Basel)        ISSN: 2075-4418


1. Introduction

Salmonella species are gram-negative motile facultatively anaerobic bacilli that commonly cause self-limited gastroenteritis [1]. It is transmitted via the ingestion of contaminated food and water or rattlesnake meat or is acquired via the fecal–oral route [2]. Although commonly benign, Salmonellae are responsible for 600 deaths annually, and up to 10% of the cases develop bacteremia, particularly among infants, young children, the elderly, and immunocompromised individuals, affecting vital systems such as the nervous and cardiovascular systems [3,4]. Endocarditis is an exceedingly rare complication of Salmonella infection with an incidence of 0.2–0.4% [5]. It is a fulminant, destructive, and invasive infection that follows a highly complicated clinical course with possible life-threatening complications, such as conduction disturbances, valvular abscesses, perforation and/or rupture, and carries a high mortality rate that exceeds 45% [5,6,7,8]. Several Salmonella serotypes have been implicated in infective endocarditis, the most common of which are S. choleraesuis, S. typhimurium, S. Thompson, and S. typhi [2]. Mitral valve Salmonella infective endocarditis comprises 33.3% of Salmonella infective endocarditis cases, whereas Salmonella mural (nonvalvular) infective endocarditis comprises 26.4%, with a higher mortality rate of 52% [2]. Multiple predisposing factors for Salmonella endocarditis have been described in the literature, including human immunodeficiency virus (HIV) infection, congenital heart diseases, and rheumatic heart disease (RHD) and subsequent prosthetic valve replacement [5,9].

2. Case Presentation

A 56-year-old Saudi female, with a known case of type 2 diabetes mellitus, hypertension, chronic anemia, atrial fibrillation, non-ischemic cardiomyopathy, and RHD status post mitral and aortic valves replacement, presented to our emergency department complaining of a month-long history of fluctuating fever, chills, and rigors, accompanied by occasional cough and mild shortness of breath. At first, she had a sore throat, cough, and sneezing, for which she visited a private clinic and was diagnosed as a case of tonsillitis and prescribed a short course of antibiotics without significant improvement. She denied a history of sick contact, chest pain, palpitations, syncope, abdominal or joint pains, urinary or bowel changes, or nausea and vomiting. Upon admission, she was on digoxin and furosemide for heart failure, warfarin for atrial fibrillation, bisoprolol and candesartan for hypertension, insulin glargine for diabetes mellitus, rosuvastatin for dyslipidemia, and esomeprazole for occasional reflux. Her past surgical history was remarkable for a MAZE procedure a year ago for atrial fibrillation and mechanical aortic (size 21 mm) and mitral (size 31 mm) valves replacement for RHD 2 years ago. Her family history was noncontributory. On examination, she was ill-appearing, normotensive (115/67 mmHg), and tachycardiac (140 bpm) with a high-grade fever (39.5 °C). The clinical examination of the respiratory system revealed the presence of right basal crepitations. Cardiovascular examination was unremarkable, with normal S1 and S2 with appreciable metallic clicks, and no added sounds or murmurs, carotid or femoral bruits, or thrills or heaves. Her abdomen was nontender and soft, with normal bowel sounds, and without evidence of organomegaly. A trace right lower limb edema was observed during examination. She was admitted under cardiology for diagnosis and management as appropriate. Laboratory investigations were notable for normocytic normochromic non-hemolytic anemia (Hgb: 115 g/L, MCV: 85.8 fL, MCHC: 330 g/L, Haptoglobin: 1.87 g/L), thrombocytopenia (Platelets: 96 × 10^9/L), abnormal liver function (ALT: 57 U/L, AST: 113 U/L, Alk Phos: 188 U/L, Total Bili: 55.9 μmol/L, GGT: 292 U/L), kidney injury (Creatinine: 264 μmol/L, BUN: 23 mg/dL, eGFR: 17 mL/min/1.73 m2), elevated uric acid (655 μmol/L), lactic acid (2.42 mmol/L), inflammatory markers (ESR: 85 mm/h, CRP: 336 mg/L, PCT: 23.7 ng/mL), cardiac biomarkers (BNP: 256 pmol/L, Troponin I: 75 pg/mL), thrombotic markers (D-dimer: 12.32 mg/L, Fibrinogen: 6.23 g/L), hypotonic hyponatremia (170 mOsm/kg, 119 mmol/L), hypochloridemia (88 mmol/L), and hypoalbuminemia (30 g/L). Her coagulation profile was remarkable for elevated PT (59.1 s), PTT (45 s), and INR (6.62) (Table 1). Urinalysis was unremarkable, and blood cultures came positive for Salmonella (group C and D) three times during the patient’s admission, despite appropriate IV antibiotics.
Table 1

Important Laboratory Values at Hospital Admission, ICU Admission/One-Day Preoperatively, Discharge, and Follow-Up.

Test NameReference Range with UnitAt Initial AdmissionAt ICU AdmissionAt DischargeAt Follow-Up
Hgb120~160 gm/L1158810098
MCV76~96 fL82.893.693.993.1
Retic Percent0.5~1.5%5.65.08N/A3.37
RBC4~5.4 × 1012/L4.212.843.163.29
WBC4~11 × 109/L10.28.257.326.88
Neutrophils2~7.5 × 109/L9.326.285.015.45
Lymphocytes1~4.4 × 109/L0.31.011.21.68
Platelets150~400 × 109/L96219288212
PTSecond55.912.236.126.3
PTTSecond41.941.636.531
INR.6.211.143.62.54
AST5~34 U/L113285234
ALT5~55 U/L57142824
Bili T~20.5 μmol/L55.939.538.828.1
Bili D~8.6 μmol/L403023.316
GGT9~36 U/L290286576627
Alk Phos40~150 U/L188281193199
Total Protein64~83 g/L65668277
BUN3.5~7.2 mmol/L2313.69.915.9
Creatinine50~98 μmol/L264190213149
eGFR~60 mL/min/1.73 m217252225
Albumin35~50 g/L30294748
Uric Acid150~370 μmol/L655363257701
Sodium136~145 mmol/L119109129136
Chloride98~107 mmol/L888094102
Phosphorus0.74~1.52 mmol/L1.181.270.871.62
Ca2.1~2.55 mmol/L1.861.872.412.33
Adj Ca2.1~2.55 mmol/L2.062.092.272.17
Potassium3.5~5.1 mmol/L4.64.75.15.1
Magnesium0.66~1.07 mmol/L0.930.80.80.8
Lactic Acid0.5~2.22.962.58N/AN/A
CRP~8 mg/L33689N/AN/A
PCT~0.05 ng/mL23.719.5N/AN/A
ESR0~30 mm/h8559N/AN/A
D-Dimer0~0.512.324.9N/AN/A
BNP~28.9 pmol/L256420N/A295
Troponin I~15.6752196N/AN/A
Creatine Kinase 29~168 U/L151455N/AN/A

Abbreviations N/A: Not available, Hgb: Hemoglobin, MCV: Mean Corpuscular Volume, RBC: Red Blood Cells, WBC: White Blood Cells, PT: Prothrombin Time, PTT: Partial Thromboplastin Time, INR: International Normalized Ratio, AST: Aspartate transaminase, ALT: Alanine aminotransferase, Bili T: Total Bilirubin, Bili D: Direct Bilirubin, GGT: Gamma-glutamyl Transferase, Alk Phos: Alkaline Phosphatase, BUN: Blood Urea Nitrogen, GFR: Glomerular Filtration Rate, Ca: Calcium, CRP: C-Reactive Protein, PCT: Procalcitonin, ESR: Erythrocyte Sedimentation Rate, BNP: Brain Natriuretic Peptide.

Chest radiograph was notable for bilateral interstitial infiltrates representing pulmonary edema (Figure 1), and admission ECG showed atrial fibrillation with a rapid ventricular response (Figure 2). A cardiac positron emission tomography/computed tomography (PET/CT scan) revealed increased Fluorodeoxyglucose (FDG) uptake around the prosthetic aortic valve and the aortic root, indicating an ongoing inflammatory or infectious process (Figure 3 and Figure 4). Cardiac CT findings were periaortic collection, extending to the anterior mediastinum along the retrosternal area, and associated with enhancing wall, mediastinal stranding, and multiple enlarged lymph nodes. Furthermore, there was a pseudoaneurysm in the ascending aorta (Figure 5). Transesophageal echocardiogram was performed and showed a posterior aortic root abscess cavity extending to the aortomitral curtain, bulging in the left atrium, and communicating with the left ventricular outflow tract. Moreover, there was moderate concentric hypertrophy, global hypokinesis of the left ventricle with an ejection fraction of 45%, and mild tricuspid regurgitation (Videos S1 and S2). After a week of admission, she developed epigastric pain, for which she underwent abdominal and pelvis CT. It demonstrated a large hypodense area in the lower pole of the spleen with surrounding fat stranding and another upper pole linear hypodensity, representing infected splenic infarction (Figure 6). A diagnosis of complicated Salmonella aortic prosthetic valve endocarditis was made, and the patient was counselled about the risk of surgical intervention, and she agreed.
Figure 1

Chest X-ray showing bilateral airspace opacities and interstitial infiltrates representing pulmonary edema.

Figure 2

ECG showing atrial fibrillation with a rapid ventricular response.

Figure 3

Cardiac PET scan showing increased FDG uptake around the prosthetic aortic valve and the aortic root, indicating an ongoing inflammatory or infectious process.

Figure 4

Cardiac CT scan showing increased FDG uptake around the prosthetic aortic valve and the aortic root, indicating an ongoing inflammatory or infectious process.

Figure 5

Cardiac CT showing periaortic collection and pseudoaneurysm in the ascending aorta.

Figure 6

Abdominal and pelvis CT showing a large hypodense area in the lower pole of the spleen with and another upper pole linear hypodensity, representing infected splenic infarction. The white arrows point at hypodense areas indicating splenic infarction.

The patient underwent a Commando procedure in which a redo sternotomy with peripheral cardiopulmonary bypass was established, infected tissues were resected, mitral valve was replaced with a 27 mm mechanical valve, aortomitral curtain and left atrial roof were reconstructed, aortic root and ascending aorta were replaced, and modified Valsalva conduit and 21 mm tissue aortic valve were implanted. Following that, she was admitted to the cardiac intensive care unit (ICU) and commenced on IV Ceftriaxone and Gentamicin. A few days after ICU admission, she became severely hypotensive and developed acute kidney injury requiring continuous renal replacement therapy in the form of hemodialysis (HD). Two weeks postoperatively, a follow-up transthoracic echocardiography demonstrated well-seated aortic and mitral valves, mild aortic regurgitation, and localized posterior pericardial effusion. After 18 days of ICU admission, she was shifted to the floor and commenced on conventional HD via perma-cath thrice weekly. She was discharged after 4 months of admission, asymptomatic and hemodynamically stable with a negative septic workup. On follow-up 2 months later, she stopped HD, and the perma-cath was removed. Overall, she was healthy, with good urine output and stable kidney function (Creatinine: 149 μmol/L, BUN: 15.9 mg/dL) (Figure S1).

3. Discussion

Salmonella species are Gram-negative bacilli that commonly cause self-limited gastroenteritis but may infect the meninges, bones, myocardium, and other vital organs [1,3,4]. Endocarditis is an exceedingly rare complication of Salmonella infection with an incidence of 0.2–0.4% and a high mortality rate even with appropriate antibiotics therapy [5]. It is a fulminant, destructive, and highly invasive disease that is possibly complicated by conduction defects, valvular abscesses, perforation, and/or rupture [6,7,8]. It usually occurs in patients with HIV and preexisting heart diseases, including congenital heart diseases and RHD [5,9]. In this article, we report a case of Salmonella prosthetic valve endocarditis complicated by splenic infarction, prolonged hospital stay, and kidney injury in a 56-year-old female with multiple cardiovascular comorbidities. We believe that this case is interesting for the following reasons. (1) This case highlights the importance of maintaining a high index of clinical suspicion for Salmonella endocarditis in patients with prosthetic valves who present with bacteremia, especially in the absence of extracardiac sources of infection such as IV catheters and pneumonia. Early recognition and surgical intervention are essential to decrease Salmonella endocarditis morbidity, such as conduction abnormalities, septic embolism, valvular abscesses, perforation or rupture, and mortality [10]. (2) To the best of our knowledge, this might be the second case of Salmonella prosthetic valve endocarditis in the Kingdom of Saudi Arabia, but the first case of aortic valve Salmonella endocarditis, as the previously reported case was Salmonella mitral valve endocarditis [11]. (3) This case is unique because the patient had double prosthetic valves (mitral and aortic), and her case was uniquely complicated by splenic infarction due to septic emboli, aortic pseudoaneurysm, and aortic root abscess cavity extending to the aortomitral curtain, bulging in the left atrium, and communicating with the left ventricular outflow tract. This might be the first case of aortic pseudoaneurysm as a complication of Salmonella prosthetic valve endocarditis. Although cerebral embolism is a known complication of Salmonella endocarditis [12,13,14,15], splenic infarction due to emboli in the setting of Salmonella endocarditis has only been reported once [16]. (4) The patient’s age is atypical for salmonella endocarditis, as most of the reported cases were younger than 50 years [4]. (5) Salmonella prosthetic valve endocarditis is extremely rare, and to the best of our knowledge, only around 20 cases have been reported in the literature. The Modified Duke criteria consist of clinical, laboratory, and imaging findings that are used in the diagnosis of endocarditis. The diagnosis of endocarditis requires two major criteria, one major and three minor criteria, or five minor criteria [17]. In this case, three blood cultures came positive for Salmonella during the patient’s admission and PET/CT with FDG and cardiac CT findings were highly suggestive of endocarditis. Based on the European Society of Cardiology, findings suggestive of endocarditis on ECG-gated cardiac CT angiogram or PET/CT with FDG are considered major criteria [17]. Additionally, the reported case meets some of the minor criteria, such as having a predisposing heart condition and persistent fever of ≥38.0 °C (≥100.4 °F). Salmonella is an intestinal pathogen, but it can invade the epithelium, flourish intracellularly, and, through the lymphatic system, spread systemically [5]. Nontyphoidal Salmonella is of particular interest, as it can invade the arterial intima and therefore infect the endothelium in the presence of atherosclerosis through a poorly understood mechanism [18]. In our patient, multiple blood cultures came positive for nontyphoidal Salmonella (group C and D), which could explain her aortic involvement. Based on the few reported cases, it seems that patients with HIV or preexisting cardiac disease, especially those aged ≥ 50 years, might be more vulnerable to salmonella endocarditis [5,9], but it has been reported in normal heart valves [19,20]. Our patient had a history of RHD previously treated by double prosthetic valve replacement, atrial fibrillation, and cardiomyopathy. Old data showed poor efficacy for antibiotics in the treatment of Salmonella endocarditis [10], but more recent data showed that third generation cephalosporins, such as Ceftriaxone, and fluoroquinolones are often effective [5]. Besides surgery, our patient was treated with IV Ceftriaxone and Gentamicin. Although highly complicated and risky, surgical intervention has been shown to greatly improve survival and should be considered in patients with extensive disease [21].

4. Conclusions

Salmonella prosthetic valve endocarditis represents a small fraction but a life-threatening form of Salmonella endocarditis. Since unified diagnostic criteria are lacking, Salmonella endocarditis represents a diagnostic challenge, and clinicians should maintain a low threshold of its diagnosis, especially in patients with preexisting heart disease, as early medical and surgical interventions can prevent or mitigate its associated morbidity and mortality.
  21 in total

Review 1.  Visiting the cell biology of Salmonella infection.

Authors:  Amit Lahiri; Ayan Lahiri; Namrata Iyer; Priyanka Das; Dipshikha Chakravortty
Journal:  Microbes Infect       Date:  2010-06-09       Impact factor: 2.700

2.  High incidence of intravascular focus in nontyphoid Salmonella bacteremia in the age group above 50 years: a population-based study.

Authors:  H Nielsen; K O Gradel; H C Schønheyder
Journal:  APMIS       Date:  2006-09       Impact factor: 3.205

Review 3.  Salmonella Serogroup C: Current Status of Vaccines and Why They Are Needed.

Authors:  Fabien J Fuche; Ousmane Sow; Raphael Simon; Sharon M Tennant
Journal:  Clin Vaccine Immunol       Date:  2016-09-06

4.  Cardiac conduction abnormalities preceding transoesophageal echocardiographic evidence of perivalvar extension of infection in a case of Salmonella prosthetic valve endocarditis.

Authors:  M I Miyamoto; A M Hutter; J H Blum; D F Torchiana
Journal:  Heart       Date:  1997-10       Impact factor: 5.994

Review 5.  Salmonella infective endocarditis.

Authors:  Wan-Ling Cheng; Chia-Wen Li; Ming-Chi Li; Nan-Yao Lee; Ching-Chi Lee; Wen-Chien Ko
Journal:  J Microbiol Immunol Infect       Date:  2015-03-24       Impact factor: 4.399

6.  2015 ESC Guidelines for the management of infective endocarditis: The Task Force for the Management of Infective Endocarditis of the European Society of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the European Association of Nuclear Medicine (EANM).

Authors:  Gilbert Habib; Patrizio Lancellotti; Manuel J Antunes; Maria Grazia Bongiorni; Jean-Paul Casalta; Francesco Del Zotti; Raluca Dulgheru; Gebrine El Khoury; Paola Anna Erba; Bernard Iung; Jose M Miro; Barbara J Mulder; Edyta Plonska-Gosciniak; Susanna Price; Jolien Roos-Hesselink; Ulrika Snygg-Martin; Franck Thuny; Pilar Tornos Mas; Isidre Vilacosta; Jose Luis Zamorano
Journal:  Eur Heart J       Date:  2015-08-29       Impact factor: 29.983

7.  Salmonella prosthetic valve endocarditis. A case report.

Authors:  Y H Lee; L P Lai; K G Shyu; P Kuan; W P Lien
Journal:  Angiology       Date:  1994-03       Impact factor: 3.619

Review 8.  Extensive Salmonella enteritidis endocarditis involving mitral, tricuspid valves, aortic root and right ventricular wall.

Authors:  Halil Mutlu; Jawad Babar; Peter R Maggiore
Journal:  J Am Soc Echocardiogr       Date:  2009-01-10       Impact factor: 5.251

9.  Simultaneous Salmonella spp. endocarditis and mycotic abdominal aortic aneurysm presentation: a surgical dilemma.

Authors:  Kanwal Kumar; Darren H Freed; Rakesh C Arora; John J Y Lee
Journal:  Interact Cardiovasc Thorac Surg       Date:  2009-05-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.