Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Endocr Pract. 2022 Oct;28(10):1062-1068. doi: 10.1016/j.eprac.2022.07.008. Epub 2022 Jul 20.
Hypercalcemia is sometimes observed in patients with cirrhosis, but very little is known about the epidemiology in patients with hypercalcemia of chronic liver disease (HCLD) or how its presence may modulate the overall mortality risk. We assessed the associations between the clinical and laboratory characteristics of patients with HCLD with 90-day mortality.
A systematic search of the medical records at our institution over a 10-year period was performed to retrospectively identify subjects with HCLD during inpatient admission. Univariate and multivariable regression analyses were performed to detect the risk factors for all-cause 90-day mortality.
Thirty-eight subjects with HCLD were identified using stringent inclusion and exclusion criteria to exclude individuals with other secondary causes of hypercalcemia. A total of 35 subjects had 90-day vital status available, which revealed 40% mortality. The model for end-stage liver disease sodium score and duration of inpatient hypercalcemia were positively associated with mortality with respective odds ratios of 1.23 (95% CI, 1.06-3.23) and 1.24 (95% CI, 1.04-1.49) in a univariate regression model and 1.30 (95% CI, 1.04-1.62) and 1.33 (95% CI, 1.04-1.71) in a multivariable regression model. The admission and peak serum calcium levels were not associated with mortality. Only 6 subjects received bisphosphonates or calcitonin during their admission, limiting our ability to assess the impact of treatment on outcomes.
In patients admitted to the hospital with HCLD, the duration of hypercalcemia was positively associated with 90-day mortality, providing a potential interventional target to reduce mortality in this high-risk population. Studies to validate the utility of treating hypercalcemia are required.
肝硬化患者有时会出现高钙血症,但对于慢性肝病高钙血症(HCLD)患者的流行病学或其存在如何调节整体死亡率风险知之甚少。我们评估了 HCLD 患者的临床和实验室特征与 90 天死亡率之间的关系。
对我院 10 年来的病历进行系统检索,以回顾性确定住院期间 HCLD 患者。进行单变量和多变量回归分析,以检测全因 90 天死亡率的危险因素。
使用严格的纳入和排除标准排除其他继发性高钙血症患者后,确定了 38 例 HCLD 患者。共有 35 例患者有 90 天的生存状态,死亡率为 40%。终末期肝病模型钠评分和住院期间高钙血症的持续时间与死亡率呈正相关,在单变量回归模型中,各自的比值比分别为 1.23(95%CI,1.06-3.23)和 1.24(95%CI,1.04-1.49),在多变量回归模型中,各自的比值比分别为 1.30(95%CI,1.04-1.62)和 1.33(95%CI,1.04-1.71)。入院和峰值血清钙水平与死亡率无关。仅 6 例患者在住院期间接受了双膦酸盐或降钙素治疗,限制了我们评估治疗对结局影响的能力。
在因 HCLD 住院的患者中,高钙血症的持续时间与 90 天死亡率呈正相关,为降低这一高危人群的死亡率提供了一个潜在的干预目标。需要研究来验证治疗高钙血症的效用。