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缺铁与青紫型屏气发作:铁剂治疗的有效性

Iron deficiency and cyanotic breath-holding spells: The effectiveness of iron therapy.

作者信息

Hamed Sherifa A, Gad Eman Fathalla, Sherif Tahra Kamel

机构信息

a Department of Neurology and Psychiatry , Assiut University Hospital , Assiut , Egypt.

b Department of Pediatrics , Children's Hospital, Assiut University , Assiut , Egypt.

出版信息

Pediatr Hematol Oncol. 2018 Apr;35(3):186-195. doi: 10.1080/08880018.2018.1491659. Epub 2018 Oct 23.

Abstract

Frequent cyanotic breath holding spells cause fear and severe anxiety to parents. This study aimed to evaluate clinical, laboratory and treatment characteristics of children with cyanotic breath holding spells. Included were 180 children (mean age: 1.82 ± 0.53 years) with cyanotic breath holding spells. They were divided into three groups: with iron deficiency, with iron deficiency anemia and without iron deficiency. Blood hemoglobin (HB), ferritin and iron concentrations were measured at baseline and after 3 and 6 months of iron treatment. The mean spell frequency was 24.57 ± 7.31/months, 83% had spells after the age of 1 year, 37% had daily spells, 16% had family history of spells, and 61% had Iron deficiency/Iron deficiency anemia ( = .001). No significant difference in the frequency of spells between children with iron deficiency and those with Iron deficiency anemia. Compared to patients without iron deficiency, there was significant reduction of spells frequency, increased hemoglobin, ferritin and iron levels after 3 and 6 months of iron therapy ( = .0001). Negative correlations were observed between spell frequency with hemoglobin ( = .001), ferritin ( = .0001) and iron ( = .001) levels. Not only Iron deficiency anemia but also iron deficiency alone without anemia is associated with a risk of high-frequency cyanotic breath holding spells. Iron therapy results in reduction in spells' frequency which was correlated with increasing ferritin and iron levels.

摘要

频繁的青紫型屏气发作会让家长感到恐惧和严重焦虑。本研究旨在评估青紫型屏气发作患儿的临床、实验室及治疗特征。研究纳入了180例青紫型屏气发作患儿(平均年龄:1.82±0.53岁)。他们被分为三组:缺铁组、缺铁性贫血组和无缺铁组。在基线时以及铁剂治疗3个月和6个月后测量血血红蛋白(HB)、铁蛋白和铁浓度。平均发作频率为24.57±7.31次/月,83%的患儿在1岁后发作,37%的患儿每天发作,16%的患儿有发作家族史,61%的患儿有缺铁/缺铁性贫血(P = 0.001)。缺铁患儿和缺铁性贫血患儿之间的发作频率无显著差异。与无缺铁的患儿相比,铁剂治疗3个月和6个月后发作频率显著降低,血红蛋白、铁蛋白和铁水平升高(P = 0.0001)。发作频率与血红蛋白(P = 0.001)、铁蛋白(P = 0.0001)和铁(P = 0.001)水平之间存在负相关。不仅缺铁性贫血,而且单纯缺铁而无贫血也与高频青紫型屏气发作风险相关。铁剂治疗可降低发作频率,这与铁蛋白和铁水平升高相关。

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