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护理肺血流量增加性病变的患者。

Caring for patients with lesions increasing pulmonary blood flow.

作者信息

Moynihan P J, King R

出版信息

Crit Care Nurs Clin North Am. 1989 Jun;1(2):195-213.

PMID:2818877
Abstract

The most common congenital cardiac defect is VSD. This malady accounts for 20 to 30 per cent of all congenital cardiac defects and is representative of a cardiac lesion that increases pulmonary blood flow. Although lesions, which increase pulmonary blood flow, may vary in incidence, they frequently have common symptomatology. Over time, congestive heart failure becomes a problem. Poor respiratory status leads to weight loss, poor feeding, and failure to thrive. If unrepaired, the child often presents with cyanosis and tachypnea. The history may include frequent respiratory infections, exercise intolerance, generalized malaise, or fatigue. In spite of poor weight gain, the child may be edematous and have a large liver. Definitive diagnosis of each lesion may be made by echocardiogram, cardiac catheterization, or both. With these data and a detailed history, treatment and management decisions are determined. In most cases, as the child gets older, symptoms become more evident. This is the result of high pulmonary pressure. High pressure over time causes a thickening of the alveolar tissue, which decreases the permeability of the alveolar membranes for gas exchange. Lung changes can become irreversible, but it is unusual for irreversible changes to occur before 1 year of age. All the lesions described in this article are amendable to primary repair before 1 year of age, affording the best functional results. Postoperative nursing care includes management of persisting CHF and PVR while maintaining adequate cardiac output. Many factors, including electrolyte balance, nutritional status, conduction disturbances, stress, and parental anxiety, influence the management of these infants. The outcome depends greatly on the assessment skill of a highly competent cardiac intensive care nurse and an environment conducive to collaborative practice.

摘要

最常见的先天性心脏缺陷是室间隔缺损。这种疾病占所有先天性心脏缺陷的20%至30%,是一种增加肺血流量的心脏病变的代表。虽然增加肺血流量的病变发病率可能有所不同,但它们通常有共同的症状。随着时间的推移,充血性心力衰竭会成为一个问题。呼吸状态不佳会导致体重减轻、喂养困难和发育不良。如果不进行修复,患儿常出现紫绀和呼吸急促。病史可能包括频繁的呼吸道感染、运动不耐受、全身不适或疲劳。尽管体重增加不佳,但患儿可能出现水肿并有肝脏肿大。每种病变的明确诊断可通过超声心动图、心导管检查或两者来确定。根据这些数据和详细病史,确定治疗和管理决策。在大多数情况下,随着患儿年龄的增长,症状会变得更加明显。这是高肺压的结果。随着时间的推移,高压会导致肺泡组织增厚,从而降低肺泡膜进行气体交换的通透性。肺部变化可能会变得不可逆转,但在1岁之前出现不可逆转的变化并不常见。本文所述的所有病变在1岁之前都适合进行一期修复,以获得最佳的功能结果。术后护理包括在维持足够心输出量的同时管理持续存在的充血性心力衰竭和肺血管阻力。许多因素,包括电解质平衡、营养状况、传导障碍、压力和家长焦虑,都会影响对这些婴儿的管理。结果在很大程度上取决于一位能力出众的心脏重症监护护士的评估技能以及有利于协作实践的环境。

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