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Belgisch tijdschrift voor geneeskunde最新文献

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[Hematodinium].
Pub Date : 2022-01-07 DOI: 10.1079/cabicompendium.101400
A. Hutsebaut
This datasheet on Hematodinium covers Identity, Hosts/Species Affected.
本数据表包括血液病的身份,宿主/受影响物种。
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引用次数: 0
[Differential leukocyte count]. [白细胞差异计数]。
Pub Date : 2020-02-08 DOI: 10.32388/bcp669
M. D. DE GROODT
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引用次数: 6
[Leukorrhea]. (白带)。
Pub Date : 2020-02-07 DOI: 10.32388/jvbd7p
M. Thiery
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引用次数: 3
Congenital diaphragmatic hernia 先天性膈疝
Pub Date : 2017-08-30 DOI: 10.5772/INTECHOPEN.69362
J. Baerg, Arul S. Thirumoorthi, Rajaie Hazboun
Despite advances in neonatal and surgical care, the management of congenital diaphrag‐ matic hernia (CDH) remains challenging with no definitive standard treatment guide‐ lines. Several centers report mortality rates as low as 20%, but if extracorporeal membrane oxygenation (ECMO) support is required, the mortality rate rises to 50%. The disease severity is related to the degree of pulmonary hypoplasia and pulmonary hypertension that occurs with CDH. Both conditions decrease the infant’s ability to ventilate and oxy‐ genate adequately at delivery. These physiologic conditions that impair gas exchange are the important determinants of morbidity and mortality in CDH infants. Presently, delivery of infants with CDH is recommended close to term gestation. The focus of care includes gentle ventilation, hemodynamic monitoring, and treatment of pulmonary hypertension followed by surgery for the defect. Extracorporeal membrane oxygenation (ECMO) is considered after failure of conventional medical management for infants ≥ 34 weeks’ gestation or with weight >2 kg and no associated major lethal anomalies. This chapter discusses long‐term follow‐up recommendations for survivors, which should involve a multidisciplinary approach, as there are many surgical and nonsurgical conse‐ quences to the disease process. Clinical strategies that address these multifaceted aspects of care, from prenatal to long‐term follow‐up, may further reduce the high mortality rate for these infants.
尽管新生儿和外科护理取得了进展,但先天性膈疝(CDH)的治疗仍然具有挑战性,没有明确的标准治疗指南。一些中心报告死亡率低至20%,但如果需要体外膜氧合(ECMO)支持,死亡率上升至50%。疾病的严重程度与CDH伴发的肺发育不全和肺动脉高压的程度有关。这两种情况都会降低婴儿在分娩时的通气和充氧能力。这些损害气体交换的生理条件是CDH婴儿发病率和死亡率的重要决定因素。目前,CDH婴儿的分娩建议接近足月妊娠。护理的重点包括轻度通气、血流动力学监测和肺动脉高压治疗,随后进行手术治疗。对于妊娠≥34周或体重> 2kg且无相关重大致死异常的婴儿,在常规医疗管理失败后考虑体外膜氧合(ECMO)。本章讨论了对幸存者的长期随访建议,这应该涉及多学科方法,因为疾病过程中有许多手术和非手术后果。从产前到长期随访,解决这些多方面护理的临床策略可能会进一步降低这些婴儿的高死亡率。
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引用次数: 1
[Sedare dolorem]. [痛苦地坐着]。
P Regniers
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引用次数: 0
[Problems in the commercial airplane transport of patients with cardiopulmonary disease]. [心肺疾病患者的商用飞机运输问题]。
P Vermeire
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引用次数: 0
[Treatment of aplastic anemia]. [治疗再生障碍性贫血]。
W van Hove
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引用次数: 0
[Indications and contra-indications for oxygen therapy and respiratory analeptics]. 氧疗和呼吸镇痛药的适应症和禁忌症。
J Tasson
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引用次数: 0
[Anti-allergic therapy]. 抗过敏治疗。
R Colle
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引用次数: 0
[Treatment of rheumatoid arthritis]. 类风湿关节炎的治疗。
A Vermeulen
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引用次数: 0
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