Successful treatment of infective endocarditis due to pandrug-resistant Klebsiella pneumoniae with ceftazidime-avibactam and aztreonam

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作者
Majed F. Alghoribi
Moayad Alqurashi
Liliane Okdah
Bassam Alalwan
Yahya S. AlHebaishi
Abdulmajeed Almalki
Maha A. Alzayer
Abdulrahman A. Alswaji
Michel Doumith
Mazin Barry
机构
[1] King Abdullah International Medical Research Center,Infectious Diseases Research Department
[2] King Saud Bin Abdulaziz University for Health Sciences,Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City (KAMC)
[3] Ministry of National Guard Health Affairs (MNGHA),Division of Adult Infectious Diseases, Department of Medicine
[4] Prince Sultan Military Medical City,Department of Adult Cardiology
[5] Prince Sultan Cardiac Center,Division of Infectious Diseases, College of Medicine
[6] King Saud University,undefined
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Pandrug-resistant (PDR) K. pneumoniae refractory to conventional treatment has been reported worldwide, causing a huge burden on the healthcare system, patient safety and the economy. K. pneumoniae is a prominent opportunistic pathogen causing hospital-acquired and community-acquired infections, but is rarely associated with infective endocarditis. Currently, there are sparse data guiding the optimal regimen when commonly used antibiotics fail, notably for the treatment of endocarditis infections. Here we report our experience in treating a 40-year-old female with PDR K. pneumoniae infection of cardiovascular implantable electronic device (CIED) and right-sided infective endocarditis. Initial susceptibility testing of the incriminated pathogen showed an apparent susceptibility to colistin but the prolonged course of colistin, gentamicin and meropenem did not resolve the infection. However, the synergistic combinations of aztreonam with ceftazidime-avibactam was able to overcome resistance and clear the infection rapidly. Genome sequencing showed that the PDR K. pneumoniae isolate belongs to the international high-risk clone ST14. The isolate harbored genes encoding NDM-1, OXA-48, CTX-M-14b, SHV-28 and OXA-1, explaining resistance to all β-lactams, including carbapenems. It carried the armA gene conferring resistance to all clinically important aminoglycosides and had alterations in GyrA, ParC and MgrB, explaining resistance to ciprofloxacin and colistin.
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