中国妇幼健康研究
中國婦幼健康研究
중국부유건강연구
CHINESE JOURNAL OF MATERNAL AND CHILD HEALTH RESEARCH
2015年
3期
522-524,525
,共4页
宁宁%王社教%郑向红%何长武
寧寧%王社教%鄭嚮紅%何長武
저저%왕사교%정향홍%하장무
妊娠期%甲状腺功能减退%左甲状腺素钠%剂量
妊娠期%甲狀腺功能減退%左甲狀腺素鈉%劑量
임신기%갑상선공능감퇴%좌갑상선소납%제량
pregnancy%hypothyroidism%levothyroxine%dose
目的:以妊娠期甲状腺功能减退症患者为研究对象,比较亚临床和临床甲减左甲状腺素钠( L-T4)治疗剂量在不同孕期的变化,以期对妊娠期L-T4的补充提供不同的参考依据。方法观察56例亚临床甲减和37例临床甲减妊娠期患者L-T4的剂量,比较不同妊娠周期两类患者L-T4需求量的变化。结果亚临床甲减患者在妊娠12周和20周达到L-T4饱和剂量的人数比例分别为17.9%和21.4%,而在临床甲减组中仅分别有10.8%和16.2%,两组中共约95.0%的患者在≤28周时达到饱和剂量;整个妊娠期内,亚临床甲减组L-T4总增加剂量百分比均较临床甲减组高,分别为第12周(54.55% vs 36.25%,t=2.621,P=0.010)、第20周(86.74% vs 55.04%,t=2.873,P=0.005)、第28周(111.81% vs 81.53%,t=2.224,P=0.029)和第36周(112.6% vs 82.88%,t=2.150,P=0.034)。结论不同类型甲减患者L-T4替代治疗的剂量变化规律有所差异,临床甲减患者更需密切监测甲状腺激素水平和增加剂量直至妊娠28周,而亚临床甲减患者L-T4剂量增加率较临床甲减高。
目的:以妊娠期甲狀腺功能減退癥患者為研究對象,比較亞臨床和臨床甲減左甲狀腺素鈉( L-T4)治療劑量在不同孕期的變化,以期對妊娠期L-T4的補充提供不同的參攷依據。方法觀察56例亞臨床甲減和37例臨床甲減妊娠期患者L-T4的劑量,比較不同妊娠週期兩類患者L-T4需求量的變化。結果亞臨床甲減患者在妊娠12週和20週達到L-T4飽和劑量的人數比例分彆為17.9%和21.4%,而在臨床甲減組中僅分彆有10.8%和16.2%,兩組中共約95.0%的患者在≤28週時達到飽和劑量;整箇妊娠期內,亞臨床甲減組L-T4總增加劑量百分比均較臨床甲減組高,分彆為第12週(54.55% vs 36.25%,t=2.621,P=0.010)、第20週(86.74% vs 55.04%,t=2.873,P=0.005)、第28週(111.81% vs 81.53%,t=2.224,P=0.029)和第36週(112.6% vs 82.88%,t=2.150,P=0.034)。結論不同類型甲減患者L-T4替代治療的劑量變化規律有所差異,臨床甲減患者更需密切鑑測甲狀腺激素水平和增加劑量直至妊娠28週,而亞臨床甲減患者L-T4劑量增加率較臨床甲減高。
목적:이임신기갑상선공능감퇴증환자위연구대상,비교아림상화림상갑감좌갑상선소납( L-T4)치료제량재불동잉기적변화,이기대임신기L-T4적보충제공불동적삼고의거。방법관찰56례아림상갑감화37례림상갑감임신기환자L-T4적제량,비교불동임신주기량류환자L-T4수구량적변화。결과아림상갑감환자재임신12주화20주체도L-T4포화제량적인수비례분별위17.9%화21.4%,이재림상갑감조중부분별유10.8%화16.2%,량조중공약95.0%적환자재≤28주시체도포화제량;정개임신기내,아림상갑감조L-T4총증가제량백분비균교림상갑감조고,분별위제12주(54.55% vs 36.25%,t=2.621,P=0.010)、제20주(86.74% vs 55.04%,t=2.873,P=0.005)、제28주(111.81% vs 81.53%,t=2.224,P=0.029)화제36주(112.6% vs 82.88%,t=2.150,P=0.034)。결론불동류형갑감환자L-T4체대치료적제량변화규률유소차이,림상갑감환자경수밀절감측갑상선격소수평화증가제량직지임신28주,이아림상갑감환자L-T4제량증가솔교림상갑감고。
Objective To compare the changes of levothyroxine (L-T4) dose in pregnant women with subclinical and overt hypothyroidism, so as to provide evidence for L-T4 supplement at gestational period. Methods The variations of L-T4 doses were observed and compared between 56 cases with subclinical hypothyroidism and 37 cases with overt hypothyroidism during different pregnant periods. Results In the subclinical hypothyroidism group, there were 17. 9% and 21. 4% cases reaching definitive therapeutic dosage in the 12th and 20th week of pregnancy, respectively, and there were 10. 8% and 16. 2% in the overt hypothyroidism group. In two groups, about 95. 0% cases reached definitive therapeutic dosage within 28th week. In the subclinical hypothyroidism group, the increased dose percent ( L-T4 final dose/L-T4 dose before pregnancy,%) was higher than in the other group during the whole pregnancy, and they were 12th week (54. 55%vs 36. 25%,t=2. 621,P=0. 010), 20th week (86. 74% vs 55. 04%, t=2. 873,P=0. 005), 28th week (111. 81% vs 81. 53%,t=2. 224,P=0. 029) and 36th week (112. 6% vs 82. 88%,t=2. 150,P=0. 034), respectively. Conclusion During the pregnancy, the dose variations of L-T4 substitutive therapy are different among cases of different types. The thyroid hormone level and dose increase should be monitored more closely until 28th week for cases of overt hypothyroidism. The increased dose percent is higher in cases of subclinical hypothyroidism.