成人甲状腺功能减退症的临床管理模式:中东和非洲医生的电子调查

S. Beshyah, I. Sherif, H. Mustafa, H. Saadi
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Results: Out of complete 397 responses, 368 were eligible for inclusion in the analysis. The majority were endocrinologists and internal medicine specialists; 82.2% of them have been in clinical practice for 10 years or more. Overt hypothyroidism would be treated using L-T4 alone by 97.2% of respondents; 1.7% would use a combination of L-T4 and liothyronine (L-T3) therapy. The rate of replacement would be gradual (66.5%), an empiric dose, adjusted to achieve target levels (14.7%); or a calculated full replacement dose (18.5%). A target thyroid-stimulating hormone (TSH) of 2.0–2.9 mU/L was favored in the index case of overt hypothyroidism (by 34.4%) followed by a target of 3.0–3.9 mU/L (by 26.0%) of respondents. However, a target of 4.0–4.9 mU/L was the most commonly selected TSH target for an octogenarian (by 33.5% of respondents). 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引用次数: 6

摘要

背景:甲状腺功能减退是一种常见的内分泌疾病,被广泛的医生治疗。在中东和非洲(MEA)地区没有关于甲状腺功能减退症临床管理模式的数据。目的:我们试图记录MEA地区原发性甲状腺功能减退症管理的现行做法,并将其与其他地区的国际建议和做法进行比较。材料和方法:邀请MEA相关学科的执业医师进行网络调查,包括先前验证的多项选择题,涉及一般和三种特殊情况下显性原发性甲状腺功能减退的指标病例的调查和治疗。结果:在完整的397个应答中,368个符合纳入分析的条件。大多数是内分泌学家和内科专家;临床执业10年及以上的占82.2%。97.2%的应答者单纯使用L-T4治疗明显的甲状腺功能减退;1.7%的患者将使用L-T4和碘甲状腺原氨酸(L-T3)联合治疗。替代率将是渐进的(66.5%),一个经验剂量,调整以达到目标水平(14.7%);或者计算出的完全替代剂量(18.5%)。在明显甲状腺功能减退的指标病例中,目标促甲状腺激素(TSH)为2.0-2.9 mU/L(34.4%),其次是目标3.0-3.9 mU/L(26.0%)。然而,对于一个80多岁的人来说,4.0-4.9 mU/L的TSH目标是最常见的选择(33.5%的受访者)。尽管达到了目标TSH,但持续的甲状腺功能减退症状会促使86.9%的应答者检查其他原因,5.8%的应答者改变为L-T4加L-T3治疗,4.6%的应答者增加甲状腺激素剂量。对持续性症状的评估包括全血细胞计数(82.4%)、完全代谢组(68.7%)、晨间皮质醇(65.3%)、维生素B12水平(54.5%)和血清T3水平(27.9%)。9.0%的应答者会在没有进一步理由的情况下治疗TSH为7.8 mU/L的亚临床疾病,或存在甲状腺过氧化物酶抗体阳性(65.3%)、甲状腺功能减退(65.0%)、高低密度脂蛋白(51.7%)或甲状腺肿(36.7%)。28.5%的应答者对新怀孕患者的TSH目标为2.0-2.4 mU/L, 15.8%的应答者倾向于TSH目标为1.5-1.9 mU/L。62.9%的孕妇每4周检查一次甲状腺激素水平,17.6%的孕妇每8周检查一次甲状腺激素水平。对于TSH为0.5 mU/L的甲状腺功能减退患者,怀孕后立即增加L- t4剂量的比例仅为28.5%。结论:调查显示:(1)几乎完全倾向于单独使用L-T4进行治疗,(2)使用年龄特异性TSH靶点进行替代治疗,(3)治疗轻度甲状腺功能衰竭的阈值较低,(4)孕妇和孕前妇女对TSH靶点的自满和可变关注,以及(5)对显性疾病恢复甲状腺功能正常状态的比率和方法变化很大。检测到与指南的对齐和偏离。结果应有助于指导该区域的重点教育活动,为今后监测实践提供基线。
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Patterns of clinical management of hypothyroidism in adults: An electronic survey of physicians from the Middle East and Africa
Background: Hypothyroidism is a common endocrine disorder that is managed by a wide range of physicians. There are no data on the pattern of clinical management of hypothyroidism in the Middle East and Africa (MEA) region. Objectives: We sought to document current practices in the management of primary hypothyroidism in the MEA region and compare these with international recommendations and practices elsewhere. Materials and Methods: A convenience sample of physicians practicing in the MEA in relevant disciplines were invited to take a web-based survey consisting of previously validated multiple-choice questions dealing with investigation and treatment of an index case of overt primary hypothyroidism in general and in three special situations. Results: Out of complete 397 responses, 368 were eligible for inclusion in the analysis. The majority were endocrinologists and internal medicine specialists; 82.2% of them have been in clinical practice for 10 years or more. Overt hypothyroidism would be treated using L-T4 alone by 97.2% of respondents; 1.7% would use a combination of L-T4 and liothyronine (L-T3) therapy. The rate of replacement would be gradual (66.5%), an empiric dose, adjusted to achieve target levels (14.7%); or a calculated full replacement dose (18.5%). A target thyroid-stimulating hormone (TSH) of 2.0–2.9 mU/L was favored in the index case of overt hypothyroidism (by 34.4%) followed by a target of 3.0–3.9 mU/L (by 26.0%) of respondents. However, a target of 4.0–4.9 mU/L was the most commonly selected TSH target for an octogenarian (by 33.5% of respondents). Persistent hypothyroid symptoms despite achieving a target TSH would prompt testing for other causes by 86.9% of respondents, a change to L-T4 plus L-T3 therapy by 5.8%, and an increase in the thyroid hormone dose by 4.6%. Evaluation of persistent symptoms would include measurements of complete blood count (82.4%), complete metabolic panel (68.7%), morning cortisol (65.3%), Vitamin B12 levels (54.5%), and serum T3 levels (27.9%). Subclinical disease with a TSH 7.8 mU/L would be treated without further justification by 9.0% of respondents, or in the presence of positive thyroid peroxidase antibodies (65.3%), hypothyroid symptoms (65.0%), high low-density lipoprotein (51.7%), or a goiter (36.7%). The TSH target for a newly pregnant patient was 2.0–2.4 mU/L for 28.5% of respondents, with 15.8% preferring a TSH target of 1.5–1.9 mU/L. Thyroid hormone levels would be checked every 4 weeks during pregnancy by 62.9% and every 8 weeks by an additional 17.6%. A hypothyroid patient with a TSH of 0.5 mU/L who becomes pregnant would receive an immediate L-T4 dose increase by only 28.5% of respondents. Conclusions: The survey revealed that (1) nearly exclusive preference for L-T4 alone for therapy, (2) use of age-specific TSH targets for replacement therapy, (3) a low threshold for treating mild thyroid failure, (4) complacent and variable attention to TSH targets in the pregnant and prepregnant woman, and (5) a highly variable approach to both the rate and means of restoring euthyroid status for overt disease. Both alignments with and divergence from guidelines were detected. The results should help in directing focused educational activities in the region, providing a baseline for future monitoring of practices.
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