Clinical research of 30 premature infants with lowhypotriiodothyronine syndrome
-
摘要:
目的 观察低三碘甲状腺原氨酸(T3)综合征对早产儿的影响。 方法 按照纳入标准及排除标准选取2019年1—12月蚌埠医学院第一附属医院新生儿病房住院的早产儿作为研究对象,在生后4~7 d及第4周采集空腹静脉血2 mL,应用电化学发光法测定血清促甲状腺激素(TSH)、游离三碘甲状腺原氨酸(FT3)及三碘甲状腺原氨酸(T3)水平。依据诊断标准将诊断为低T3的30例早产儿作为观察组,同胎龄甲状腺功能正常的30例早产儿作为对照组,2组患儿性别、胎龄等一般资料比较差异无统计学意义(均P > 0.05),均给予相同的基础支持治疗。观察2组早产儿在黄疸持续时间、喂养不耐受、住院天数、恢复出生体重天数、纠正胎龄40周时NBNA评分方面的差异。 结果 2组早产儿生后4~7 d的T3值(t=-19.042, P < 0.001)、FT3值(t=-22.041, P < 0.001)比较差异有统计学意义,生后4周的T3值(t=-1.933, P=0.059)及FT3值(t=-1.622, P=0.110)比较差异无统计学意义。2组早产儿黄疸持续时间(t=2.759, P=0.008)、喂养不耐受(χ2=8.531, P=0.003)、住院天数(t=6.471, P < 0.001)、恢复出生体重天数(t=6.584, P < 0.001)比较差异有统计学意义,2组早产儿纠正胎龄40周NBNA评分比较差异无统计学意义(t=-1.842, P=0.071)。 结论 低T3综合征患儿较正常甲状腺功能患儿的黄疸持续时间、住院天数及恢复出生体重时间延长,喂养不耐受发生率高,但短期神经发育无明显差异。 -
关键词:
- 低三碘甲状腺原氨酸综合征 /
- 喂养不耐受 /
- 生长发育 /
- 早产儿
Abstract:Objective To observe the adverse effects of low hypotriiodothyronine (T3) syndrome on premature infants. Methods Thirty premature infants hospitalised in the neonatal ward of The First Affiliated Hospital of Bengbu Medical College from January to 2019 to December 2019 were selected. About 4 to 7 days and 4 weeks after birth, 2 mL of fasting venous blood was collected from the infants. Serum thyroid-stimulating hormone (TSH), free triiodothyronine (FT3) and triiodothyronine (T3) were determined via electrochemiluminescence. According to the diagnostic criteria, premature infants diagnosed with low T3 were taken as the observation group (n=30), whereas premature infants with normal thyroid functions at the same gestational age were taken as the control group (n=30). No statistical difference was observed in the general conditions of the two groups (P > 0.05), both group were given with the same basic supportive treatment. Differences in the duration of jaundice, feeding intolerance, hospitalisation days, days of birth weight recovery and neonatal behavior neurological assessment (NBNA)test scores at 40 weeks of gestational age were observed between the two groups. Results Between the two groups, T3 levels at 4 to 7 days after birth (t=-19.042, P < 0.001) and FT3 levels at 4 weeks after birth (t=-22.041, P < 0.001) were statistically significant. At 4 weeks after birth, T3 levels (t=-1.933, P=0.059) and FT3 levels (t=-1.622, P=0.110) were not statistically significant. The differences in jaundice duration (t=2.759, P=0.008), feeding intolerance (χ2=8.531, P=0.003), hospitalisation days (t=6.471, P < 0.001) and birth weight recovery days (t=6.584, P < 0.001) were statistically significant between the two groups. However, no statistically significant difference (t=-1.842, P=0.071) was observed in NBNA scores between the two groups at the correct gestational age of 40 weeks. Conclusion Children with a low T3 syndrome have longer jaundice durations, hospitalisation days and weight recovery times, as well as a higher incidence of feeding intolerance, than children with normal thyroid functions. Nevertheless, their short-term neurodevelopment was not significantly influenced. -
表 1 2组早产儿一般资料比较(x ±s)
组别 例数 性别(男/女, 例) 胎龄(周) 分娩方式(剖/顺, 例) 出生体重(kg) 5 min Apgar评分(分) 败血症(例) SNAPPE-Ⅱ(分) 观察组 30 18/12 33.82±1.63 19/11 2.07±0.24 7.03±1.65 14 22.73±4.41 对照组 30 16/14 33.90±1.58 15/15 2.13±0.35 7.70±1.68 12 25.10±5.21 统计量 0.271a -1.064b 1.086a -0.792b 1.548b 0.271a 1.899b P值 0.602 0.288 0.297 0.432 0.127 0.602 0.062 注:a为χ2值,b为t值。 表 2 2组早产儿血清T3及FT3比较(x ±s)
组别 例数 T3(nmol/L) FT3(pmol/L) 生后4~7 d 生后4周 生后4~7 d 生后4周 观察组 30 0.43±0.12 1.49±0.13 1.64±0.36 4.32±0.54 对照组 30 1.29±0.22 1.57±0.19 3.71±0.36 4.53±0.47 t值 -19.042 -1.933 -22.041 -1.622 P值 < 0.001 0.059 < 0.001 0.110 表 3 2组早产儿临床指标比较(x ±s)
组别 例数 黄疸持续时间(d) 喂养不耐受(例) 住院天数(d) NBNA评分(分) 恢复出生体重天数(d) 观察组 30 12.13±3.75 17 21.50±3.8 35.33±1.49 14.83±2.18 对照组 30 9.97±2.11 6 15.27±3.63 36.13±1.85 11.20±2.09 统计量 2.759a 8.531b 6.471a -1.842a 6.584a P值 0.008 0.003 < 0.001 0.071 < 0.001 注:a为t值,b为χ2值。 -
[1] 李轶, 徐南平. 危重症神经内分泌激素的变化[J]. 实用临床医学, 2015, 16(4): 104-107. https://www.cnki.com.cn/Article/CJFDTOTAL-LCSY201504044.htm [2] SOTO-RIVERA C L, FICHOROVA R N, ALLRED E N, et al. The relationship between TSH and systemic inflammation in extremely preterm newborns[J]. Endocrine, 2015, 48(2): 595-602. doi: 10.1007/s12020-014-0329-4 [3] 齐薛浩, 杨琳. 早产儿甲状腺功能的研究进展[J]. 中国妇幼健康研究, 2016, 27(4): 530-532. doi: 10.3969/j.issn.1673-5293.2016.04.038 [4] 缪克凡, 段蔚, 钱燕, 等. 早产儿暂时性低甲状腺素血症、低三碘甲状腺原氨酸综合征影响因素分析[J]. 中华儿科杂志, 2013, 51(8): 607-611. doi: 10.3760/cma.j.issn.0578-1310.2013.08.011 [5] DUTTA S, SINGH B, CHESSELL L, et al. Guidelines for feeding very low birth weight infants[J]. Nutrients, 2015, 7(1): 423-442. doi: 10.3390/nu7010423 [6] JACOB H, PETERS C. Screening, diagnosis and management of congenital hypothyroidism: European Society for Paediatric Endocrinology Consensus Guideline[J]. Arch Dis Child Educ Pract Ed, 2015, 100(5): 260-263. doi: 10.1136/archdischild-2014-307738 [7] ARMANIAN A M, KELISHADI R, BAREKATAIN B, et al. Frequency of thyroid function disorders among a population of very-low-birth-weight premature infants[J]. Iran J Neonatol, 2016, 7(3): 9-16. http://ijn.mums.ac.ir/article_7649_720b61af86045306c820a5086c906053.pdf [8] AKTAS O N, GURSOY T, SOYSAL E, et al. Thyroid hormone levels in late preterm, early term and term infants: a study with healthy neonates revealing reference values and factors affecting thyroid hormones[J]. J Pediatr Endocrinol Metab, 2017, 30(11): 1191-1196. http://europepmc.org/abstract/MED/29132242 [9] ARMANIAN A M, KELISHADI R, BAREKATAIN B, et al. Frequency of thyroid function disorders among a population of very-low-birth-weight premature infants[J]. IJN, 2016, 7(3): 9-16. http://ijn.mums.ac.ir/article_7649_720b61af86045306c820a5086c906053.pdf [10] 赵雪琼. 早产儿甲状腺功能低下的发生情况及相关因素研究[J]. 中国妇幼保健, 2018, 33(19): 4443-4445. https://www.cnki.com.cn/Article/CJFDTOTAL-ZFYB201819041.htm [11] LEE J, KIM S W, JEON G W, et al. Thyroid dysfunction in very low birth weight preterm infants[J]. Korean J Pediatr, 2015, 58(6): 224-229. doi: 10.3345/kjp.2015.58.6.224 [12] NAZARPOUR S, RAMEZANI TEHRANI F, SIMBAR M, et al. Thyroid dysfunction and pregnancy outcomes[J]. Iran J Reprod Med, 2015, 13(7): 387-396. [13] LA FRANCHI S H. Screening preterm infants for con-genital hypothyroidism: better the second time around[J]. J Pediatr, 2014, 164(6): 1259-1261. doi: 10.1016/j.jpeds.2014.02.031 [14] LEGER J, OLIVIERI A, DONALDSON M, et al. European Society for Paediatric Endocrinology consensus guide-lines on screening, diagnosis, and management of congenital hypothyroidism[J]. J Clin Endocrinol Metab, 2014, 99(2): 363-384. doi: 10.1210/jc.2013-1891 [15] 曾纪赞, 关健强, 谢克开, 等. 左旋甲状腺素片治疗早产儿暂时性甲状腺功能减退症的临床观察[J]. 中国现代医药杂志, 2016, 18(10): 36-37. https://www.cnki.com.cn/Article/CJFDTOTAL-ZHTY201610011.htm [16] CUESTAS E, GAIDO M I, CAPRA R H. Transient neo-natal hyperthyrotropinemia is a risk factor for developing persistent hyperthyrotropinemia in childhood with repercussion on developmental status[J]. Eur J Endocrinol, 2015, 172(4): 483-490. doi: 10.1530/EJE-13-0907 [17] TRUMPFF C, DE SCHEPPER J, VANDERFAEILLIE J, et al. Neonatal thyroid-stimulating hormone concentration and psychomotor development at preschool age[J]. Arch Dis Child, 2016, 101(12): 1100-1106. doi: 10.1136/archdischild-2015-310006 [18] SILVA M H, ARAUJO M C, DINIZ E M, et al. Thyroid abnormalities in term infants with fungal sepsis[J]. Rev Assoc Med Bras(1992), 2016, 62(6): 561-567. doi: 10.1590/1806-9282.62.06.561
点击查看大图
表(3)
计量
- 文章访问数: 144
- HTML全文浏览量: 152
- PDF下载量: 6
- 被引次数: 0