Nichols Gregory A, Alexander Charles M, Girman Cynthia J, Kamal-Bahl Sachin J, Brown Jonathan B
Kaiser Permanente Center for Health Research, Portland, Oregon 97227-1098, USA.
Endocr Pract. 2007 Jan-Feb;13(1):37-44. doi: 10.4158/EP.13.1.37.
To revise older estimates of secondary failure that may no longer describe the contemporary pattern of sulfonylurea (SU) monotherapy and to identify predictors of such failure.
We identified 4,091 patients who achieved hemoglobin A1c (A1C) <8% within 1 year after initiation of SU therapy as their first-ever antihyperglycemic drug after January 1, 1996. The study subjects underwent follow-up until they added or switched antihyperglycemic medication, had A1C > or =8%, or terminated health plan membership or until December 31, 2004. We defined secondary failure by using two separate but overlapping approaches: (1) the addition of or switch to another antihyperglycemic drug after 6 months of SU therapy or (2) the first A1C measurement > or =8.0%.
The level of A1C achieved within 1 year after initiation of SU treatment was the most powerful predictor of secondary SU failure. About 50% of patients whose best A1C was 7.0% to 7.9% added or switched antihyperglycemic drugs within 40 months, whereas it took nearly 60 months for those in the 6.0% to 6.9% A1C category and 74 months in the A1C <6.0% category to reach a 50% failure rate. Similarly, more than half of those patients whose best A1C was 7.0% to 7.9% had an A1C value > or =8% within 24 months, whereas it took nearly 60 months for study subjects in the 6.0% to 6.9% A1C category and 86 months for those in the <6.0% category to have SU failure. Younger age and weight gain were also predictive of failure.
Secondary failure of SU therapy is inversely associated with the level of A1C achieved within the first year of SU monotherapy. Clinicians should quickly consider therapeutic adjustments to lower the A1C level rapidly if initial success is not achieved.
修正可能不再适用于描述当代磺脲类药物(SU)单药治疗模式的继发性失效的既往估计,并确定此类失效的预测因素。
我们纳入了4091例患者,这些患者在1996年1月1日之后开始使用SU治疗作为其首个降糖药物,且在1年内糖化血红蛋白(A1C)<8%。研究对象接受随访,直至他们添加或更换降糖药物、A1C≥8%、终止健康计划成员资格或至2004年12月31日。我们采用两种独立但重叠的方法定义继发性失效:(1)SU治疗6个月后添加或更换另一种降糖药物;(2)首次A1C测量值≥8.0%。
SU治疗开始后1年内达到的A1C水平是SU继发性失效最有力的预测因素。最佳A1C为7.0%至7.9%的患者中,约50%在40个月内添加或更换了降糖药物,而A1C在6.0%至6.9%的患者达到50%失效率需要近60个月,A1C<6.0%的患者则需要74个月。同样,最佳A1C为7.0%至7.9%的患者中,超过一半在24个月内A1C值≥8%,而A1C在6.0%至6.9%的研究对象达到SU失效需要近60个月,<6.0%的患者则需要86个月。年龄较小和体重增加也是失效的预测因素。
SU治疗的继发性失效与SU单药治疗第一年达到的A1C水平呈负相关。如果未取得初始成功,临床医生应迅速考虑进行治疗调整以快速降低A1C水平。