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两例与左甲状腺素品牌更换相关的治疗失败病例。

Two cases of therapeutic failure associated with levothyroxine brand interchange.

作者信息

Copeland P M

机构信息

North Shore Medical Center, Salem Hospital, MA 01970, USA.

出版信息

Ann Pharmacother. 1995 May;29(5):482-5. doi: 10.1177/106002809502900505.

Abstract

OBJECTIVE

To report the loss of therapeutic control in 2 hypothyroid patients and remind clinical pharmacists and other healthcare professionals to remain cognizant of possible product quality differences within or bioequivalency differences between levothyroxine products.

CASE SUMMARIES

Two patients with stable hypothyroidism experienced symptoms of hypothyroidism with increased serum thyroid-stimulating hormone (TSH) concentrations after switching from 1 levothyroxine product to another. One tablet from 1 of the patient's levothyroxine prescriptions was assayed, and its levothyroxine content was 74.5% of the label claim, a value outside of the United States Pharmacopeia requirements of 90-110%.

DISCUSSION

Two patients with hypothyroidism had remained euthyroid and stable while receiving 1 levothyroxine product, but became symptomatic with dramatically increased serum TSH concentrations while receiving what were thought to be comparable dosages of another levothyroxine product. Therapeutic control was reestablished in both patients after therapy with the original levothyroxine product was reinstated.

CONCLUSIONS

Clinical pharmacists and other healthcare professionals should remain cognizant of possible product quality differences within or bioequivalency differences between levothyroxine products. These differences necessitate close monitoring of hypothyroid patients, counseling these patients about the clinical signs of sub- and supratherapeutic levothyroxine dosages, and prudence when switching patients with stable hypothyroidism to alternative levothyroxine products. If there are inconsistencies between levothyroxine products, resultant deleterious effects on the therapeutic stability of patients with hypothyroidism may undermine cost savings that might be incurred by such a change. If these patients are switched to alternative levothyroxine products, it is recommended that thyroid function tests be repeated after equilibration to the new product.

摘要

目的

报告2例甲状腺功能减退患者治疗控制的丧失情况,并提醒临床药师和其他医疗保健专业人员注意左甲状腺素产品内部可能存在的产品质量差异或生物等效性差异。

病例摘要

2例甲状腺功能减退病情稳定的患者,在从一种左甲状腺素产品换用另一种产品后,出现甲状腺功能减退症状,血清促甲状腺激素(TSH)浓度升高。对其中1例患者的一份左甲状腺素处方中的1片药进行了分析,其左甲状腺素含量为标签标示量的74.5%,该值超出了美国药典90%-110%的要求。

讨论

2例甲状腺功能减退患者在服用一种左甲状腺素产品时甲状腺功能正常且病情稳定,但在服用被认为剂量相当的另一种左甲状腺素产品时出现症状,血清TSH浓度显著升高。在用原来的左甲状腺素产品恢复治疗后,2例患者的治疗控制均得以重新建立。

结论

临床药师和其他医疗保健专业人员应注意左甲状腺素产品内部可能存在的产品质量差异或生物等效性差异。这些差异需要密切监测甲状腺功能减退患者,向这些患者告知左甲状腺素剂量低于或高于治疗量的临床体征,并在将病情稳定的甲状腺功能减退患者换用其他左甲状腺素产品时谨慎行事。如果左甲状腺素产品之间存在不一致性,由此对甲状腺功能减退患者治疗稳定性产生的有害影响可能会削弱这种更换可能带来的成本节约。如果将这些患者换用其他左甲状腺素产品,建议在适应新产品后重复进行甲状腺功能检查。

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