Daptomycin ,is the first approved member of a new class of antimicrobials, the cyclic lipopeptides, and presents selective action against gram-positive bacteria, including methicillin- and vancomycin-resistant strains,disrupting the transfer of amino acids in the cell membrane, thus hindering the biosynthesis of bacterial cell cell wall peptide polysaccharide, changing the properties of cytoplasm membrane, can destroy bacterial cell membrane function in many ways, and quickly kill gram-positive bacteria. Because of its unique chemical structure and sterilization mechanism, bacteria rarely develop resistance to daptomycin. Daptomycin can be reversibility combined with human plasma protein (mainly serum albumin) and metabolized mainly through the kidneys. There is still a lot of controversy about the application of daptomycin in patients with severe illness. Although studies suggest that daptomycin has less damage to kidney function than vancomycin, the effect of daptomycin on kidney function in severely ill patients is not yet clear, and more clinical studies are needed to explore their relationship. In addition, it is not clear whether the physiological pathology of specific populations such as sepsis/infectious shock, acute kidney injury, (AKI), hypoproteinemia, and renal replacement treatment affects the pharmacokinetics/pharmacodynamics of Daptomycin. By exploring the application of daptomycin in patients with severe illness, this study explores the effects of special pathological physiological states such as sepsis/infectious shock and hypoproteinemia on daptomycin PK/PD, as well as the effects of different hemoglobin concentrations of daptomycin on the outcome of kidney function.
Study Type
OBSERVATIONAL
Enrollment
120
Adult patients are given the recommended dose of daptomycin for injection. Patients with creatinine clearance (CLCR) ≥ 30 mL / min: 6 mg / kg every 24 hours. Patients with creatinine clearance (CLCR) \<30mL / min (including hemodialysis or peritoneal dialysis): 6mg / kg every 48 hours. Dissolve 6mg / kg of this drug in 0.9% sodium chloride injection and instill it over a 30-minute time course once every 24 or 48 hours.
Zhongnan Hospital of Wuhan University
Wuhan, Hubei, China
Apparent volume of distribution
Apparent volume of distribution of daptomycin in the patient's blood
Time frame: 1 week
Peak plasma concentration
Peak plasma concentration of daptomycin
Time frame: 1 week
Plasma trough concentration
Plasma trough concentration of daptomycin
Time frame: 1 week
Area under the plasma concentration versus time curve (AUC)
Area under the plasma concentration versus time curve (AUC) of daptomycin
Time frame: 1 week
Clearance of daptomycin
Daptomycin is metabolized mainly by the kidneys
Time frame: 1 week
Half-life
Half-life of plasma daptomycin
Time frame: 1 week
Protein binding rate
Reversible binding of daptomycin to plasma proteins (mainly serum albumin)
Time frame: 1 week
Serum creatinine
Serum creatinine can reflect kidney function
Time frame: 1 week
Urine output
Urine volume can reflect kidney function
Time frame: 1 week
Blood Urea Nitrogen
It can reflect kidney function
Time frame: 1 week
Urine protein
Reflect kidney function
Time frame: 1 week
Cystatin C
Reflect kidney function
Time frame: 1 week
β2-microglobulin(β2-MG)
Reflect kidney function
Time frame: 1 week
Major Adverse kidney Event(MAKE)
Major Adverse kidney Event(MAKE)Refers to death, need for renal replacement therapy, and creatinine levels that are twice or more the baseline value;It can reflects the outcome of renal function.
Time frame: 28days
ICU mortality
Reflect patient prognosis
Time frame: 28days
In-hospital mortality
Reflect patient prognosis
Time frame: 28days
ICU hospital stay length
Reflect patient prognosis
Time frame: 28 days
Total hospital stay length
Reflect patient prognosis
Time frame: 28 days
White blood cell count
Reflect the severity of the patient's infection
Time frame: 1 week
Neutrophil ratio
Reflect the severity of the patient's infection
Time frame: 1 week
C-Reactive Protein
Reflect the severity of the patient's infection
Time frame: 1 week
Procalcitonin
Reflect the severity of the patient's infection
Time frame: 1 week
Interleukin-6
Reflect the severity of the patient's infection
Time frame: 1 week
Bacterial culture results
Reflect the severity of the patient's infection
Time frame: 1 week
Body temperature
Reflect the severity of the patient's infection
Time frame: 1 week
Vascular drug use days
Assess patients' systemic circulation
Time frame: 1 week
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