- General Drug Summary
- Description
- An amino acid that occurs in vertebrate tissues and in urine. In muscle tissue, creatine generally occurs as phosphocreatine. Creatine is excreted as creatinine in the urine. [PubChem]
- Also Known As
- (alpha-Methylguanido)acetic acid; Creatine (8CI); Creatine, hydrate; Methylguanidoacetic acid; N-Amidinosarcosine; N-Methyl-N-guanylglycine
- Groups
- approved; nutraceutical
- Structure
- Summary In Neonatal Jaundice
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1 record(s) for Creatine NA in Neonatal Jaundice.
- PMID
- Drug Name
- Efficacy
- Evidence
- 1489851
- Creatine
- NA
- Review
- Summary
- The interference of creatine in serum of bilirubin can be determinated by three automatic analysers.
- Creatinine and automatic analysers in relation to icteric specimens. European journal of clinical chemistry and clinica, 1992 Nov [Go to PubMed]
- A study is described on the interference of bilirubin with the determination of creatine in serum using three automatic analysers i.e. the Technicon Chem-1, the DuPont Dimension and the Baxter Paramax. In all instruments a kinetic Jaffé reaction is applied. As comparison method we used a HPLC based selected method. All methods proved to be sensitive to interference, the Paramax showing the best performance with our set of specimens. Results regarding modifications leading to improvement and possible future experiments are discussed.
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1 record(s) for Creatine Effective in Maintaining Remission in Neonatal Jaundice.
- PMID
- Drug Name
- Efficacy
- Evidence
- 22883035
- Creatine
- Effective in Maintaining Remission
- Clinical Trial
- Summary
- Creatine kinase (CK), MB isoenzymes of creatine kinase (CK-MB), and cardiac troponin-I (cTnI) were measured to test the function of myocardial.
- [Clinical study of myocardial damage induced by neonatal jaundice in normal birth weight term infants]. Zhonghua er ke za zhi. Chinese journal of pediatri, 2012 May [Go to PubMed]
- To clarify whether neonatal jaundice may cause myocardial damage to term infants with normal birth weight (BW).
Totally 178 term neonates admitted during March, 2004 to December, 2010 with normal BW were enrolled. Infants with antenatal or neonatal asphyxia, temperature abnormality, septicemia, antenatal viral infection, congenital dysmorphia, congenital heart disease, 21-trisomy, and polycythemia were excluded. There was no maternal complications during the pregnancy. Serum total bilirubin (TB), creatine kinase (CK), MB isoenzymes of creatine kinase (CK-MB), and cardiac troponin-I (cTnI) were measured. Patients with transcutaneous bilirubin level (TcB) ≥ 342 µmol/L (20 mg/dl) were in Group A (n = 32), and those with TcB below phototherapy level at matched time point were in Group B (n = 25). ECG, for correct Q-T intervals (QTc) and correct QT intervals dispersion (QTcd), and ECHO, for left ventricular ejection fraction (EF), the ratio of the peak velocity of early stage and advanced stage of diastolic phase at the mitral orifice (E/A), were applied to patients in Group A and B. SPSS 13.0 software was used forthe data analysis. The coefficients of correlation among age in hours on admission (hr), TB, CK, CK-MB, CK-MB/CK, and cTnI were studied by multiple and partial correlation analysis. Data in Group A and B were compared by independent-samples Mann-Whitney U test (nonparametric method) or Student t-test.
When the data were analyzed by multiple correlation, there were significant correlation between TB and cTnI, CK-MB, respectively (r = 0.212, -0.161, respectively, all P < 0.05). But, when the data were analyzed by partial correlation, there was no correlation between TB and cTnI, CK-MB, respectively (r' = 0.112, -0.112, respectively, all P > 0.05), negative correlation between hr and TB, cTnI, respectively (r' = -0.490, P = 0.000; r' = -0.162, P = 0.032). There was no significant difference in CK (Z = -1.384, P = 0.166), CK-MB (Z = -0.821, P = 0.412), cTnI (Z = -1.159, P = 0.246), QTc (t = 1.146, P = 0.257), QTcd (t = 1.342, P = 0.185), EF (t = 1.558, P = 0.125), E/A (t = -0.640, P = 0.525) between group A and B. There was significant difference in CK-MB/CK (Z = -3.187, P = 0.001) between group A and B with a lower value in group A [0.075 (0.032 - 0.102)] comparing to that in group B [0.160 (0.073 - 0.284)].
There is no sufficient evidence to support the hypothesis that neonatal jaundice may induce myocardial damage in normal birth weight term infants.