|Year : 2020 | Volume
| Issue : 4 | Page : 154-157
Bacterial endocarditis diagnosed with point-of-care ultrasound in a rural emergency department
Taft Micks1, Kyle Sue2
1 Brandon Regional Health Centre, Brandon, MB, Canada
2 Discipline of Family Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Canada
|Date of Submission||12-Sep-2019|
|Date of Decision||08-Oct-2019|
|Date of Acceptance||28-Oct-2019|
|Date of Web Publication||28-Sep-2020|
MD, MHM, BSc, CCFP (PC) Kyle Sue
Discipline of Family Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Micks T, Sue K. Bacterial endocarditis diagnosed with point-of-care ultrasound in a rural emergency department. Can J Rural Med 2020;25:154-7
|How to cite this URL:|
Micks T, Sue K. Bacterial endocarditis diagnosed with point-of-care ultrasound in a rural emergency department. Can J Rural Med [serial online] 2020 [cited 2022 Jan 19];25:154-7. Available from: https://www.cjrm.ca/text.asp?2020/25/4/154/296491
| Introduction|| |
Bacterial endocarditis (BE) is defined as the infection of a native or prosthetic heart valve, the surface of the endocardium or an intracardiac device. It is rare but notoriously difficult to diagnose promptly with devastating morbidity and mortality for delayed definitive management. It may be even more difficult in rural resource-limited settings, without the investigative capabilities of a tertiary care centre. BE is a condition infrequently seen in rural emergency departments. There are few epidemiologic studies on its rural incidence. One study in rural New York found 4.4 cases/100,000 person years for people 18 years or older. The worldwide incidence estimates range from 3 to 10/100,000 people yearly. However, despite its rarity, BE can be life-threatening. In-hospital mortality reaches 20% and 6-month mortality reaches 30%, which is worse than many malignancies. Delayed or missed diagnosis is extremely common, which contributes to the high morbidity and mortality, as definitive management is delayed. The clinical presentation is quite varied and non-specific, and, as Osler observed, 'Few diseases present greater difficulties in the way of diagnosis than malignant endocarditis, difficulties which in many cases are practically insurmountable.' A study in Japan noted that it took a median of 14 days for definitive diagnosis of BE, which resulted in 65% of patients receiving inappropriate antibiotics. Unsurprisingly, 80% of those who died in the study were recipients of inappropriate antibiotics.
However, with increasing emergency department use of point-of-care ultrasound (POCUS), physicians now have an additional tool that can help them more promptly diagnose BE.
| Case Report|| |
A 34-year-old female presented to our rural emergency department with a 3-week history of progressive pedal oedema and worsening 'rash' to her lower legs bilaterally. She denied any other symptoms such as chest pain, shortness of breath, B symptoms and increased bleeding, or bruising. She did admit to intravenous drug use with various opiates. Her past medical history was otherwise unremarkable. Her initial vital signs were as follows: blood pressure 95/65, heart rate 132 bpm (sinus), temperature 36.7°C (peripheral) and 38.6°C (rectal), respiratory rate 20/min and SpO296% on room air.
Physical examination revealed an unkempt female with poor hygiene. Her 'rash' was bilateral petechiae extending from her forefoot to her knees, in addition to pedal oedema. There were no signs of petechiae or ecchymosis elsewhere. Her cardiovascular examination revealed a normal S1/S2, no S3/S4 and no obvious murmur. She had good air entry to both bases with no associated wheezes, rhonchi or crackles. She did not have any splinter haemorrhages or Janeway lesions. Her examination was otherwise unremarkable.
Her initial investigations revealed a white blood cell count of 25 × 10/L, haemoglobin of 79 g/L and platelets of 45 × 10/L. Her sodium was 116 mmol/L, potassium was 4 mmol/L, chloride was 74 mmol/L, creatinine was 331 μmol/L, urea was 26.5 mmol/L, troponin was 14 ng/L and erythrocyte sedimentation rate was 47. Her initial venous blood gas was pH 7.40/PaCO234 mmHg/HCO322 mmHg/base excess −3 mmol/L with a lactate of 3.5 mmol/L. Her chest X-ray revealed multiple septic emboli.
POCUS was performed revealing a vegetative lesion on her tricuspid valve [Figure 1], confirming the diagnosis of BE. She was started on intravenous piperacillin-tazobactam 4.5 g and vancomycin 2 g, as per our septic protocol, and transferred to the nearest intensive care unit. The next day, her Gram stain revealed Gram-positive cocci in clusters, likely representing Staphylococcusaureus.
|Figure 1: Ultrasound – subxiphoid view of the heart (*-vegetative lesion extending over both sides of the tricuspid valve, TV: Tricuspid valve, RV: Right ventricle, RA: Right atrium, LV: Left ventricle, LA: Left atrium).|
Click here to view
| Discussion|| |
Despite the rarity of BE, it is a clinical entity with high morbidity and mortality, for which prompt diagnosis and definitive treatment can make a major difference in outcome. Factors that place the rural population at higher risk include an older age demographic with higher rates of diabetes. Other risk factors include intracardiac devices, prosthetic valves, haemodialysis, cancer, congenital heart disease and intravenous drug use., Most cases have delayed diagnosis and delayed definitive treatment, due to challenges in diagnosis. Clinical manifestations are notoriously non-specific. Pathognomonic signs, such as Janeway lesions and Osler nodes, are rare. Even a murmur is only present in 85% and a fever in 90% of patients presenting with BE. Furthermore, 10% have blood cultures that show no growth.
Rural emergency departments are often resource limited, with some lacking even basic laboratory investigation capabilities. However, portable ultrasound machines are becoming ubiquitous, even in these settings. For native-valve endocarditis, bedside echocardiography is moderately sensitive (75%) and specific (over 90%) for detecting vegetation. POCUS can also provide information on the mechanism and haemodynamic severity of the valve lesion, along with assessment of left and right ventricular function. In the case where POCUS does not show a vegetation, but clinical suspicion is high, the next step should be a transoesophageal echocardiogram (TEE), which will generally require transport to a larger centre. Transport may be complicated by weather and the availability of a medical evacuation team, so the authors recommend transporting such a patient to a higher level of care as soon as possible, before the patient deteriorates or the transportation window closes. This should occur regardless of whether a TEE is locally available, and regardless of whether the TEE is positive or negative, as the patient will need to be in a location where cardiac surgery is available for definitive treatment. Broad-spectrum intravenous antibiotics (coverage required for methicillin-susceptible S. aureus, methicillin-resistant S. aureus, Streptococci, HACEK species, Bartonella and non-HACEK Gram-negative pathogens) should be started immediately while awaiting transport. Blood cultures should be drawn and sent together with the patient. If clinical suspicion is lower, the authors suggest coverage with the same broad-spectrum intravenous antibiotics while awaiting results from three blood cultures drawn. At the same time, they suggest continuing search for an alternate diagnosis and monitoring for additional signs from the Modified Duke Criteria [Table 1], [Box 1] to emerge., If an alternate diagnosis is found, or symptoms resolve within 4 days of antibiotic therapy, one can rule out BE. If BE is confirmed, the patient will need to be transported to a cardiac centre for potential surgery.
| Conclusion|| |
This case highlights a diagnosis made promptly in a rural emergency department using POCUS as an adjunct to history, physical examination and other investigations, which may have limited availability in rural and remote settings. Nevertheless, there remain barriers to using POCUS rurally, including insufficient training, funding, quality assurance and an inability to maintain skills as cited by rural physicians. Corrective measures must be taken so that the benefits of POCUS are extended to patients in rural Canada where, arguably, it has the greatest potential for benefit when access to advanced imaging is not readily available.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship: Nil.
Conflicts of interest: There are no conflicts of interest.
| References|| |
Cahill TJ, Prendergast BD. “Infective endocarditis.” Lancet 2016;387:882-93.
Fatima S, Dao B, Jameel A, Sharma K, Strogatz D, Scribani M, et al
. Epidemiology of infective endocarditis in rural upstate New York, 2011-2016. J Clin Med Res 2017;9:754-8.
Slipczuk L, Codolosa JN, Davila CD, Romero-Corral A, Yun J, Pressman GS, et al
. Infective endocarditis epidemiology over five decades: A systematic review. PLoS One 2013;8:e82665.
Osler W. “The Gulstonian lectures, on malignant endocarditis.” BMJ 1885;1:577-9.
Fukuchi T, Iwata K, Ohji G. “Failure of early diagnosis of infective endocarditis in Japan–a retrospective descriptive analysis.” Medicine (Baltimore) 2014;93:e237.
Habib G, Badano L, Tribouilloy C, Vilacosta I, Zamorano JL. Recommendations for the practice of echocardiography in infective endocarditis. Eur J Echocardiogr 2010;11:202-19.
Canadian Institute for Health Information. Disparities in Primary Health Care Experiences Among Canadians with Ambulatory Care Sensitive Conditions. Ottawa, ON: Canadian Institute for Health Information; 2012.
Cabell CH, Heidenreich PA, Chu VH, Moore CM, Stryjewski ME, et al
. “Increasing rates of cardiac device infections among medicare beneficiaries: 1990-1999,” Am Heart J 2004;147:582-6.
Darouiche RO. Treatment of infections associated with surgical implants. N
Engl J Med 2004;350:1422-9.
McCarthy JT, Steckelberg JM. Infective endocarditis in patients receiving long-term hemodialysis. Mayo Clin Proc 2000;75:1008-14.
Blattner K, Beazley CJ, Nixon G, Herd G, Wigglesworth J, Rogers-Koroheke MG. The impact of the introduction of a point-of-care haematology analyser in a New Zealand rural hospital with no onsite laboratory. Rural Remote Health 2019;19:4934.
Léger P, Fleet R, Maltais-Giguère J, Plant J, Piette É, Légaré F, et al
. A majority of rural emergency departments in the province of Quebec use point-of-care ultrasound: A cross-sectional survey. BMC Emerg Med 2015;15:36.
Moreillon P, Que YA. “Infective endocarditis,” Lancet 2004;363:139-49.
Habib G, Hoen B, Tornos P, Thuny F, Prendergast B, Vilacosta I, et al
. Guidelines on the prevention, diagnosis, and treatment of infective endocarditis (new version 2009): The Task force on the prevention, diagnosis, and treatment of infective endocarditis of the European society of cardiology (ESC). Endorsed by the European society of clinical microbiology and infectious diseases (ESCMID) and the international society of chemotherapy (ISC) for infection and cancer. Eur Heart J 2009;30:2369-413.
Durack D, Lukes A, Bright D, Duke Endocarditis Service. “New Criteria for Diagnosis of Infective Endocarditis: Utilization of Specific Echocardiographic Findings. The American Journal of Medicine 1994;96:200-9.
Micks T, Sue K, Rogers P. Barriers to point-of-care ultrasound use in rural emergency departments. CJEM 2016;18:475-9.