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镰状细胞贫血的肺功能研究。

Pulmonary function studies in sickle cell anaemia.

作者信息

Elegbeleye O O

出版信息

Trop Geogr Med. 1978 Dec;30(4):473-6.

PMID:749282
Abstract

Pulmonary studies including the measurements of single-breath diffusing capacity for carbon monoxide (DL); Forced Vital Capacity (FVC); Residual Volume (RV) and Total Lung Capacity (TLC) were carried out in forty normal subjects; twelve patients with homozygous sickle cell anaemia and five patients with iron deficiency anaemia due to hookworm infestation. Normal subjects had a mean haemoglobin content of 13.4 g per 100 ml and a mean DL value of 28 ml/min/mmHg. In the patients with hookworm anaemia, the mean haemoglobin was 4.9 g per 100 ml while the mean DL value was 9 ml/min per mmHg. Patients with sickle cell anaemia had a mean haemoglobin content of 6.2 g/100 ml yet the mean DL value was 20 ml/min per mmHg. The study showed that patients with homozygous sickle cell anaemia have a disproportionately high DL value in the presence of severe anaemia which might be due to a chronically expanded pulmonary capillary blood volume as a compensatory mechanism to maintain an appropriate level of DL.

摘要

肺部研究包括测量单次呼吸一氧化碳弥散量(DL)、用力肺活量(FVC)、残气量(RV)和肺总量(TLC),对40名正常受试者、12名纯合子镰状细胞贫血患者和5名因钩虫感染导致缺铁性贫血的患者进行了这些测量。正常受试者的平均血红蛋白含量为每100毫升13.4克,平均DL值为28毫升/分钟/毫米汞柱。在钩虫性贫血患者中,平均血红蛋白为每100毫升4.9克,而平均DL值为9毫升/分钟/毫米汞柱。镰状细胞贫血患者的平均血红蛋白含量为6.2克/100毫升,但平均DL值为20毫升/分钟/毫米汞柱。该研究表明,纯合子镰状细胞贫血患者在严重贫血的情况下,DL值过高,这可能是由于肺毛细血管血容量长期扩张,作为一种维持适当DL水平的代偿机制。

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Lung gas transfer in children with sickle cell anaemia.镰状细胞贫血患儿的肺气体交换
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[Respiratory function in patients with sickle cell disease (author's transl)].
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