Garg M R, Gogtay N J, Kotwani R N, Bodhe P V, Kshirsagar N A
Dept of Pharmacology, KEM Hospital, Parel, Mumbai.
J Assoc Physicians India. 1999 Apr;47(4):377-9.
Given the steep increase in the incidence of malaria in the city of Mumbai in the nineties, we decided to study the causes for the same as well as analyse the resistance pattern of P. falciparum in the city.
Smear positive cases of acute uncomplicated P. falciparum malaria who presented to us in 1994, 1995 and 1996 were analysed for their response to full dose chloroquine (25 mg/kg over 3 days). Samples of those patients who satisfied criteria for in vitro resistance testing to chloroquine and other antimalarials, were also studied. Chloroquine level in all patients was studied on Day 3 by HPLC. In vivo response to chloroquine was studied in 30, 71 and 78 patients while in vitro response was studied in 17, 35 and 30 patients respectively in the above years.
We found in vivo chloroquine resistance figures of 36.78%, 45% and 53.8% in the years '94, '95 and '96 and the in vitro resistance figures of 41.17%, 54.28% and 66.6% in the same years.
Our previous studies documenting 15% chloroquine resistance in 1993 and the increasing incidence in subsequent years suggests resistance to chloroquine as one of the causes of resurgence and maintenance of malaria in the city. If patients of uncomplicated P. falciparum malaria are to be treated with chloroquine, rigorous monitoring for nonresponse and timely rescue medication is necessary. Alternative antimalarial drugs such as mefloquine, artemisinin derivatives and sulfadoxine-pyrimethamine should be used in patients where this is not possible.
鉴于20世纪90年代孟买市疟疾发病率急剧上升,我们决定研究其原因,并分析该市恶性疟原虫的耐药模式。
对1994年、1995年和1996年前来就诊的急性非复杂性恶性疟原虫疟疾涂片阳性病例,分析其对全剂量氯喹(3天内25mg/kg)的反应。还对符合氯喹和其他抗疟药体外耐药性检测标准的患者样本进行了研究。在第3天通过高效液相色谱法研究所有患者的氯喹水平。上述年份中,分别对30例、71例和78例患者进行了氯喹的体内反应研究,对17例、35例和30例患者进行了体外反应研究。
我们发现,1994年、1995年和1996年氯喹的体内耐药率分别为36.78%、45%和53.8%,同年的体外耐药率分别为41.17%、54.28%和66.6%。
我们之前的研究记录了1993年15%的氯喹耐药率以及随后几年耐药率的上升,这表明氯喹耐药是该市疟疾复发和持续存在的原因之一。如果要用氯喹治疗非复杂性恶性疟原虫疟疾患者,必须对无反应情况进行严格监测并及时给予救援药物。在无法做到这一点的患者中,应使用甲氟喹、青蒿素衍生物和磺胺多辛-乙胺嘧啶等替代抗疟药物。