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首页> 外文期刊>Pituitary >Diagnosis, treatment and follow-up of patients with acromegaly in a clinical practice setting in Spain: the ACROPRAXIS program Delphi survey
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Diagnosis, treatment and follow-up of patients with acromegaly in a clinical practice setting in Spain: the ACROPRAXIS program Delphi survey

机译:西班牙临床实践环境中患者患者诊断,治疗和随访:Acropraxis计划Delphi调查

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摘要

Aim The ACROPRAXIS program aims to describe the management of acromegaly in Spain and provide guidance. Methods Ninety-three endocrinologists were organized into 13 panels to discuss the practical issues in managing acromegaly. Based on the key learnings, an online Delphi survey with 62 statements was performed, so those statements achieving consensus could be used as guidance. Statements were rated on a 9-point scale (9, full agreement; consensus > 66.6% of response in the same tertile). Results Ninety-two endocrinologists (98.8%) answered two rounds of the survey (mean age 47.6 years; 59.8% women; median 18.5 years of experience). Consensus was achieved for 49 (79%) statements. Diagnosis: The levels of insulin-like growth factor I (IGFI) is the preferred screening test. If IGFI levels 1-1.3 ULN, the test is repeated and growth hormone (GH) after oral glucose tolerance test (OGTT) is assessed. A pituitary magnetic resonance is performed after biochemical diagnosis. Treatment: Surgery is the first treatment choice for patients with microadenoma or macroadenoma with/without optical pathway compression. Pre-surgical somatostatin analogues (SSA) are indicated when surgery is delayed and/or to reduce anaesthesia-associated risks. After unsuccessful surgery, reintervention is performed if the residual tumor is resectable, while if non-resectable, SSA are administered. Follow-up First biochemical and clinical controls are performed 1-3 months after surgery. Disease remission is considered if random GH levels are < 1 mu g/L or OGTT is < 1 or <= 0.4 mu g/L, depending on the assay's sensitivity. Conclusion Current clinical management for acromegaly is homogeneous across Spain and generally follows clinical guidelines.
机译:旨在描述西班牙古代古代的管理并提供指导。方法有九十三个内分泌学家组织成13个面板,讨论管理棘手症的实际问题。根据关键的学习,进行了62名陈述的在线德尔福调查,因此可以将达成共识的陈述作为指导。陈述评为9分(9,全协议;共识> 66.6%的响应在同一Tertile中)。结果九十二个内分泌学家(98.8%)回答了两轮调查(平均年龄47.6岁; 59.8%妇女;中位数18.5岁的经验)。 49(79%)陈述达成共识。诊断:胰岛素样生长因子I(IGFI)的水平是优选的筛选试验。如果IGFI水平1-1.3 ULN,则重复测试,并评估口服葡萄糖耐量试验(OGTT)后的生长激素(GH)。生物化学诊断后进行垂体磁共振。治疗方法:手术是微腺瘤或Macroadenoma患者的第一个治疗选择,带有/没有光学途径压缩。手术前患有前的生长抑素类似物(SSA)在手术延迟和/或减少麻醉相关的风险时被指示。在手术不成功后,如果残留的肿瘤是可转移的,则进行重新入住,而如果施用不可切除的话,则施用SSA。手术后1-3个月进行后续前进生化和临床对照。考虑疾病缓解,如果随机GH水分<1μg/ L或OGTT是<1或<=0.4μg/ L,则取决于测定的灵敏度。结论临床临床管理在西班牙均匀均匀,一般遵循临床指南。

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