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相似文献

1
Chloramphenicol toxicity in neonates: its incidence and prevention.新生儿氯霉素毒性:其发生率及预防
Br Med J (Clin Res Ed). 1983 Nov 12;287(6403):1424-7. doi: 10.1136/bmj.287.6403.1424.
2
Efficacy of chloramphenicol in the treatment of neonatal and infantile meningitis: a study of 70 cases.
Lancet. 1983 Feb 5;1(8319):284-7. doi: 10.1016/s0140-6736(83)91697-5.
3
Chloramphenicol in paediatrics: current prescribing practice and the need to monitor.
Eur J Pediatr. 1988 Aug;147(6):574-8. doi: 10.1007/BF00442465.
4
The 'grey toddler'. Chloramphenicol toxicity.“灰色幼儿”。氯霉素毒性。
Arch Dis Child. 1974 Mar;49(3):235-7. doi: 10.1136/adc.49.3.235.
5
Initiation of chloramphenicol therapy in the newborn infant.
J Pediatr. 1982 Dec;101(6):1018-21. doi: 10.1016/s0022-3476(82)80036-x.
6
The pharmacokinetics of chloramphenicol in the neonate and young infant.
J Antimicrob Chemother. 1983 Dec;12(6):629-39. doi: 10.1093/jac/12.6.629.
7
[Need for the determination of chloramphenicol levels in the treatment of bacterial-purulent meningitis with chloramphenicol succinate in infants and small children].
Monatsschr Kinderheilkd. 1985 Apr;133(4):209-13.
8
[Chloramphenicol concentrations in serum and CSF in newborn infants and babies with bacterial meningitis (author's transl)].
Dtsch Med Wochenschr. 1981 Jun 5;106(23):739-43. doi: 10.1055/s-2008-1070392.
9
Lack of predictability of chloramphenicol toxicity in paediatric patients.
J Clin Pharm Ther. 1989 Aug;14(4):297-303. doi: 10.1111/j.1365-2710.1989.tb00250.x.
10
Use of chloramphenicol palmitate in neonates.
J Pediatr. 1984 Jul;105(1):113-6. doi: 10.1016/s0022-3476(84)80374-1.

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本文引用的文献

1
CHLORAMPHENICOL TOXICITY: CLINICAL FEATURES AND PATHOGENESIS.
Prog Hematol. 1964;4:138-59.
2
Chloramphenicol in the newborn infant. A physiologic explanation of its toxicity when given in excessive doses.新生儿使用氯霉素。过量使用时其毒性的生理学解释。
N Engl J Med. 1960 Apr 21;262:787-94. doi: 10.1056/NEJM196004212621601.
3
Fatal cardiovascular collapse of infants receiving large amounts of chloramphenicol.接受大量氯霉素治疗的婴儿发生致命性心血管虚脱。
AMA J Dis Child. 1959 Jun;97(6):761-7. doi: 10.1001/archpedi.1959.02070010763001.
4
Disposition of chloramphenicol in low birth weight infants.
Pediatrics. 1980 Oct;66(4):573-8.
5
Chloramphenicol sodium succinate kinetics in critically ill patients.危重症患者中琥珀氯霉素钠的动力学
Clin Pharmacol Ther. 1980 Jul;28(1):69-77. doi: 10.1038/clpt.1980.133.
6
Treatment of an infant with severe chloramphenicol intoxication using charcoal-column hemoperfusion.使用活性炭柱血液灌流治疗严重氯霉素中毒的婴儿。
J Pediatr. 1980 Jan;96(1):136-9. doi: 10.1016/s0022-3476(80)80350-7.
7
Exchange transfusion in acute chloramphenicol toxicity.急性氯霉素中毒的换血疗法
J Pediatr. 1981 Oct;99(4):651-3. doi: 10.1016/s0022-3476(81)80284-3.
8
Initiation of chloramphenicol therapy in the newborn infant.
J Pediatr. 1982 Dec;101(6):1018-21. doi: 10.1016/s0022-3476(82)80036-x.
9
Factors influencing the assay of antimicrobial drugs in clinical samples by the agar plate diffusion method.琼脂平板扩散法检测临床样本中抗菌药物的影响因素。
J Antimicrob Chemother. 1982 Apr;9(4):253-65. doi: 10.1093/jac/9.4.253.
10
Clinical pharmacology of two chloramphenicol preparations in children: sodium succinate (iv) and palmitate (oral) esters.
J Pediatr. 1980 Apr;96(4):757-61. doi: 10.1016/s0022-3476(80)80762-1.

新生儿氯霉素毒性:其发生率及预防

Chloramphenicol toxicity in neonates: its incidence and prevention.

作者信息

Mulhall A, de Louvois J, Hurley R

出版信息

Br Med J (Clin Res Ed). 1983 Nov 12;287(6403):1424-7. doi: 10.1136/bmj.287.6403.1424.

DOI:10.1136/bmj.287.6403.1424
PMID:6416440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1549666/
Abstract

The incidence of dose related chloramphenicol toxicity was determined in 64 neonates from 12 hospitals. Ten of the 64 exhibited symptoms attributed clinically to chloramphenicol toxicity. Nine received the dose prescribed and one an overdose. Symptoms of the grey baby syndrome were observed in five of the 10 babies; four babies suffered reversible haematological reactions; and one baby was described as very grey. Peak serum chloramphenicol concentrations in these 10 babies ranged from 28 to 180 mg/l and trough concentrations from 19 to 47 mg/l. Serum chloramphenicol concentrations above the therapeutic range (15-25 mg/l) were observed in a further 27 neonates (two had received a 10-fold overdose), none of whom showed signs of toxicity. Serious toxicity was associated with either prescription of dosages greater than that recommended or overdosage of chloramphenicol. High concentrations in young neonates may be avoided by prescribing and giving the recommended dose and then careful monitoring; concentrations should be maintained between 15 and 25 mg/l. No babies with concentrations within this range showed clinical signs of toxicity.

摘要

对来自12家医院的64名新生儿进行了与剂量相关的氯霉素毒性发生率测定。64名新生儿中有10名出现临床上归因于氯霉素毒性的症状。其中9名接受了规定剂量,1名过量用药。10名婴儿中有5名出现了灰婴综合征症状;4名婴儿出现了可逆性血液学反应;1名婴儿被描述为极度灰暗。这10名婴儿的血清氯霉素峰值浓度在28至180毫克/升之间,谷浓度在19至47毫克/升之间。另有27名新生儿的血清氯霉素浓度高于治疗范围(15 - 25毫克/升)(其中两名接受了10倍的过量用药),但均未表现出毒性迹象。严重毒性与处方剂量大于推荐剂量或氯霉素过量用药有关。通过开具并给予推荐剂量然后仔细监测,可以避免新生儿体内氯霉素浓度过高;浓度应维持在15至25毫克/升之间。在此范围内的婴儿均未表现出临床毒性迹象。