Neonatal Migratory Polycyclic Erythema of Urticaria Associated with Alprostadil: A Case Report

Thitinun Ruknoo, Jintakarn Kasemsri Na Ayutthaya, Krittiya Stonsaovapak
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Abstract

A full-term male neonate was diagnosed with complex heart disease. His diagnosis included Taussig-Bing anomaly, TGA, large subpulmonic VSD, large PDA, severe coarctation, and interrupted aortic arch. The patient was transferred to our institution, a super-tertiary care for probable management within 5 hours after birth. The 3.3 kg infant was delivered by cesarean section. Cyanosis was noted at birth. The hypoxemia and cyanosis did not improve after using an oxygen mask with bag (oxygen saturation 80%). Intubation with subsequent mechanical ventilation was initiated in this case. Ampicillin and cefotaxime were administered for possible early neonatal sepsis. An echocardiogram revealed dextro-Transposition of the great arteries (d-TGA), large subpulmonic VSD, left aortic arch, large PDA, hypoplastic aortic arch, severe coarctation, and interrupted aortic arch. Alprostadil was started within 3.5 hours after birth. Arterial switch operation (ASO) was planned. The patient’s intravenous medications included dopamine, dobutamine, fentanyl, furosemide, calcium gluconate, sodium bicarbonate, potassium chloride, ampicillin, cefotaxime, and heparin. Abstract The aim of this study was to report a case of neonatal migratory polycyclic erythema of urticaria associated with alprostadil. A full-term male neonate with complex heart disease was diagnosed. The patient had a Taussig-Bing anomaly, transposition of the great arteries (TGA), large subpulmonic ventricular septal defect (VSD), large patent ductus arteriosus (PDA), severe coarctation and interrupted aortic arch. The patient developed an adverse drug reaction during alprostadil infusion. Following the reaction, alprostadil was administered at sequentially reduced doses, and the patient eventually became tolerant of alprostadil. The patient successfully continued therapy with no further reactions or recurrences. No adverse drug reactions developed during infusion until the patient was discharged from the hospital and was transferred to a tertiary care hospital for cardiothoracic surgery.
前列地尔合并新生儿迁移性荨麻疹多环红斑1例
一个足月男婴被诊断患有复杂的心脏疾病。他的诊断包括Taussig-Bing异常,TGA,肺动脉下室间隔大,PDA大,严重缩窄,主动脉弓中断。患者在出生后5小时内转至我们的超三级护理机构。经剖宫产分娩,体重3.3公斤。出生时发绀。低氧血症和紫绀均未见明显改善(氧饱和度80%)。在本病例中开始插管并随后进行机械通气。给予氨苄西林和头孢噻肟治疗可能的早期新生儿败血症。超声心动图显示大动脉右转(d-TGA),肺动脉下室间隔大,左主动脉弓,大PDA,主动脉弓发育不全,严重缩窄,主动脉弓中断。前列地尔在出生后3.5小时内开始使用。计划动脉切换手术(ASO)。患者静脉注射的药物包括多巴胺、多巴酚丁胺、芬太尼、呋塞米、葡萄糖酸钙、碳酸氢钠、氯化钾、氨苄西林、头孢噻肟和肝素。摘要本研究报告1例新生儿迁移性荨麻疹多环红斑伴前列地尔。我们诊断了一个患有复杂心脏病的足月男婴。患者有Taussig-Bing异常,大动脉转位(TGA),肺动脉下室间隔缺损(VSD),大动脉导管未闭(PDA),严重缩窄和主动脉弓中断。患者在前列地尔输注过程中出现药物不良反应。反应后,依次减少前列地尔的剂量,患者最终对前列地尔产生耐受。患者成功地继续治疗,没有进一步的反应或复发。在输注期间没有出现药物不良反应,直到患者出院并转至三级护理医院进行心胸外科手术。
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