Impact of diagnosis and targeted interventions on the quality of life and neuropsychiatric outcomes of patients with adrenal tumours: a systematic review.

IF 5.2 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Barbara Ruggiero, Giuliana Zhu, Liam Swan, Onnicha Suntornlohanakul, Mengjie Xu, Cristina L Ronchi, Yasir S Elhassan, Derick Yates, Alessandro Prete
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引用次数: 0

Abstract

Objective: To systematically evaluate the impact of adrenal tumour diagnosis and targeted interventions on health-related quality of life (HRQoL) and neuropsychiatric outcomes across tumour subtypes.

Design: Systematic review.

Methods: A literature search of MEDLINE, Embase, Cochrane Library, and CINAHL (January 1990-March 2026) identified studies reporting HRQoL and neuropsychiatric outcomes in adults with adrenal tumours, including non-functioning adrenal tumours (NFAT), mild autonomous cortisol secretion (MACS), adrenal Cushing's syndrome (CS), primary aldosteronism (PA), phaeochromocytoma/paraganglioma (PPGL), and adrenocortical carcinoma (ACC). Study quality was assessed using CONSORT-PRO and Newcastle-Ottawa criteria. Due to methodological heterogeneity, findings were synthesized narratively.

Results: A total of 117 studies involving 35 361 patients were included. CONSORT-PRO quality was good but heterogeneous, whereas observational study quality was mostly moderate or low. Across tumour subtypes, adrenal tumours were consistently associated with impaired HRQoL and neuropsychiatric outcomes. A gradient of burden was evident, with mild impairment in NFAT, intermediate impairment in MACS and PA, and the most pronounced and persistent deficits in adrenal CS, PPGL, and ACC. Targeted interventions were often associated with improved patient-reported outcomes, though the magnitude and consistency of benefit varied across tumour subtypes and study design. Recovery was frequently incomplete. Most studies relied on generic HRQoL instruments, and no disease-specific neuropsychiatric tools were identified.

Conclusions: Adrenal tumours are associated with substantial and often persistent impairment in patient well-being across tumour subtypes. Although treatment generally improves outcomes, residual symptoms are common, underscoring the need for long-term, patient-centred care and for the development of adrenal tumour-specific patient-reported outcome measures.

诊断和针对性干预对肾上腺肿瘤患者生活质量和神经精神预后的影响:一项系统综述。
目的:系统评估肾上腺肿瘤诊断和针对性干预对不同肿瘤亚型患者健康相关生活质量(HRQoL)和神经精神预后的影响。设计:系统回顾。方法:检索MEDLINE、Embase、Cochrane Library和CINAHL(1990年1月至2026年3月)的文献,确定了报告成人肾上腺肿瘤患者HRQoL和神经精神预后的研究,包括无功能肾上腺肿瘤(NFAT)、轻度自主皮质醇分泌(MACS)、肾上腺库欣综合征(CS)、原发性醛固酮增生症(PA)、嗜铬细胞瘤/副神经节瘤(PPGL)和肾上腺皮质癌(ACC)。研究质量采用conber - pro和Newcastle-Ottawa标准进行评估。由于方法学的异质性,研究结果以叙述的方式综合。结果:共纳入117项研究,涉及35,361例患者。conber - pro质量良好,但存在异质性,而观察性研究质量大多为中等或低。在所有肿瘤亚型中,肾上腺肿瘤始终与HRQoL受损和神经精神预后相关。负担的梯度很明显,NFAT轻度损伤,MACS和PA中度损伤,肾上腺CS、PPGL和ACC最明显和持续的缺陷。有针对性的干预通常与改善患者报告的结果相关,尽管益处的大小和一致性因肿瘤亚型和研究设计而异。恢复常常是不完全的。大多数研究依赖于通用的HRQoL工具,没有确定特定疾病的神经精神病学工具。结论:肾上腺肿瘤与各种肿瘤亚型患者的健康状况存在实质性且经常持续的损害。虽然治疗通常可以改善结果,但残留症状很常见,强调需要长期的、以患者为中心的护理,并需要制定肾上腺肿瘤特异性的患者报告的结果措施。
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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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