1.Neonatal respiratory distress: recent progress in understanding pathogenesis and treatment outcomes.
Korean Journal of Pediatrics 2010;53(1):1-6
Transient tachypnea of the newborn (TTN), respiratory distress syndrome (RDS), and persistent pulmonary hypertension (PPHN) are the three most common disorders that cause respiratory distress after birth. An understanding of the pathophysiology of these disorders and the development of effective therapeutic strategies is required to control these conditions. Here, we review recent papers on the pathogenesis and treatment of neonatal respiratory disease.
Hypertension, Pulmonary
;
Parturition
;
Transient Tachypnea of the Newborn
2.Occupational Contact Urticaria Syndrome Induced by Cefotiam Dihydrochloride in a Nurse.
Hye Jeong CHOI ; Ji Youn SONG ; Young Min PARK ; Chung Won KIM ; Hyung Ok KIM
Annals of Dermatology 2003;15(3):113-115
We herein report a case of occupational contact urticaria syndrome induced by cefotiam di-hydrochloride in a nurse. She had generalized pruritic wheals accompanied by palpitations and tachypnea during the preparation of cefotiam solution. A scratch patch test with cefotiam di-hydrochloride, a major component of cefotiam ingredient showed multiple erythema and wheals within 5 minutes, accompanied by palpitations and tachypnea. No delayed type reaction was observed. Based on her clinical history and scratch test result, we diagnosed her condition as contact urticaria syndrome caused by cefotiam.
Cefotiam*
;
Erythema
;
Patch Tests
;
Tachypnea
;
Urticaria*
3.Central hyperventilation syndrome due to massive pneumocephalus after endoscopic third ventriculostomy: a case report.
Euiseok PARK ; Heezoo KIM ; Byung Gun LIM ; Dong Kyu LEE ; Dongik CHUNG
Korean Journal of Anesthesiology 2016;69(4):409-412
Pneumocephalus is common after brain surgeries, but usually is not substantial enough to cause serious complications. We recently encountered a case of post-operative tachypnea after an endoscopic 3rd ventriculostomy. At first, we thought that the hyperventilation was the result of residual paralysis after emergence from anesthesia, but during further evaluation we found a massive pneumocephalus. In such unusual post-operative situations, physicians should consider surgery-related complications as the possible cause as well, along with the anesthetic factors.
Anesthesia
;
Brain
;
Hyperventilation*
;
Paralysis
;
Pneumocephalus*
;
Postoperative Care
;
Tachypnea
;
Ventriculostomy*
4.Predictable risk factors and clinical courses for prolonged transient tachypnea of the newborn.
Ji Young CHANG ; Chang Ryul KIM ; Ellen A KIM ; Ki Soo KIM
Korean Journal of Pediatrics 2010;53(3):349-357
PURPOSE: Transient tachypnea of the newborn (TTN) is usually benign and improves within 72 hours. However, it can also progress to prolonged tachypnea over 72 hours, profound hypoxemia, respiratory failure, and even death. The aim of this study is to find predictable risk factors and describe the clinical courses and outcomes of prolonged TTN (PTTN). METHODS: The medical records of 107 newborns, >35(+0) weeks of gestational age with TTN, who were admitted to the NICU at Seoul Asan Medical Center from January 2001 to September 2007 were reviewed. They were divided into 2 groups based on duration of tachypnea. PTTN was defined as tachypnea > or =72 hours of age, and simple TTN (STTN) as tachypnea <72 hours of age. We randomly selected 126 healthy-term newborns as controls. We evaluated neonatal and maternal demographic findings, and various clinical factors. RESULTS: Fifty-five infants (51%) with total TTN were PTTN. PTTN infants had grunting, tachypnea >90/min, FiO2 >0.4, and required ventilator care more frequently than STTN infants. PTTN had lower level of serum total protein and albumin than STTN. The independent predictable risk factors for PTTN were grunting, maximal respiration rate >90/min, and FiO2 >0.4 within 6 hours of life. CONCLUSION: When a newborn has grunting, respiration rate >90/min, and oxygen requirement >0.4 of FiO2 within 6 hours of life, the infant is at high risk of having persistent tachypnea > or =72 hours. We need further study to find the way to reduce PTTN.
Anoxia
;
Gestational Age
;
Humans
;
Infant
;
Infant, Newborn
;
Medical Records
;
Oxygen
;
Respiratory Insufficiency
;
Respiratory Rate
;
Risk Factors
;
Tachypnea
;
Transient Tachypnea of the Newborn
;
Ventilators, Mechanical
5.The Effects of Inhaled Albuterol in Transient Tachypnea of the Newborn.
Myo Jing KIM ; Jae Ho YOO ; Jina JUNG ; Shin Yun BYUN
Allergy, Asthma & Immunology Research 2014;6(2):126-130
PURPOSE: Transient tachypnea of the newborn (TTN) is a disorder caused by the delayed clearance of fetal alveolar fluid. beta-adrenergic agonists such as albuterol (salbutamol) are known to catalyze lung fluid absorption. This study examined whether inhalational salbutamol therapy could improve clinical symptoms in TTN. Additional endpoints included the diagnostic and therapeutic efficacy of salbutamol as well as its overall safety. METHODS: From January 2010 through December 2010, we conducted a prospective study of 40 newborns hospitalized with TTN in the neonatal intensive care unit. Patients were given either inhalational salbutamol (28 patients) or placebo (12 patients), and clinical indices were compared. RESULTS: The duration of tachypnea was shorter in patients receiving inhalational salbutamol therapy, although this difference was not statistically significant. The duration of supplemental oxygen therapy and the duration of empiric antibiotic treatment were significantly shorter in the salbutamol-treated group. No adverse effects were observed in either treatment group. CONCLUSIONS: Inhalational salbutamol therapy reduced the duration of supplemental oxygen therapy and the duration of empiric antibiotic treatment, with no adverse effects. However, the time between salbutamol therapy and clinical improvement was too long to allow definitive conclusions to be drawn. Further studies examining a larger number of patients with strict control over dosage and frequency of salbutamol inhalations are necessary to better direct the treatment of TTN.
Absorption
;
Adrenergic beta-Agonists
;
Albuterol*
;
Humans
;
Infant, Newborn
;
Inhalation
;
Intensive Care, Neonatal
;
Lung
;
Methods
;
Oxygen
;
Prospective Studies
;
Tachypnea
;
Transient Tachypnea of the Newborn*
6.Shock after Ureteroscopic Lithotripsy: A case report.
Hyun Ju JUNG ; Sung Hak KANG ; Kyung Sil IM ; Jae Myeong LEE ; Dae Young KIM ; Sang Hyun HONG ; Jong Bun KIM
Korean Journal of Anesthesiology 2006;51(4):508-511
One of the most fearful rare complication of ureteroscopic lithotripsy is sepsis. Since sepsis after endourological maneuvers usually occur immediately after procedure, it is important to pay attention to symptoms representing sepsis such as pyrexia, tachycardia, tachypnea, and oliguria. In addition to clinical symptoms, laboratory tests including white blood cell (WBC) count, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and urine and blood cultivating can help to diagnosis of sepsis. We present a case of shock after ureteroscopic lithotripsy, which was suspected with septic shock strongly.
Blood Sedimentation
;
C-Reactive Protein
;
Diagnosis
;
Fever
;
Leukocytes
;
Lithotripsy*
;
Oliguria
;
Sepsis
;
Shock*
;
Shock, Septic
;
Tachycardia
;
Tachypnea
7.CONGENITAL CYSTIC ADENOMATOID MALFORMATION TREATED WITH EMERGENCY OPERATION.
Journal of the Korean Society of Emergency Medicine 1997;8(1):109-112
Congenital cystic adenomatoid malformation is rare form of disease causing in the lung. The main symptoms and signs are cyanosis, tachypnea, and other form of respiratory distress at or shortly after birth. In auscultation, decreased breath sound is audible and in chest X-ray, shifting of mediastinum, pulmonary herniation and depression of diaphragm are visualized with cystic shadow. We have experienced a case of cystic adenomatoid malformation of lung. After emergency operation, patients were recovered uneventfully.
Auscultation
;
Cyanosis
;
Cystic Adenomatoid Malformation of Lung, Congenital*
;
Depression
;
Diaphragm
;
Emergencies*
;
Humans
;
Lung
;
Mediastinum
;
Parturition
;
Tachypnea
;
Thorax
8.A Symptom-free Congenital Sliding Hiatal Hernia Diagnosed within 24 Hours after Birth.
Tae Ho MA ; Kyung Ah KIM ; Sun Young KO ; Yeon Kyung LEE ; Byung Hee HAN ; Son Moon SHIN
Journal of the Korean Society of Neonatology 2005;12(1):112-116
The classification of hiatal hernia is made by the position of the gastroesophageal junction. Although sliding hiatal hernia (type 1) is the most common type of hiatal hernia, it is very uncommon to be found in early infancy because it is usually symptom free. We report a case of type 1 hiatal hernia of newborn infant who had diagnosed by simple chest radiography taken because of transient tachypnea of the newborn.
Classification
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Esophagogastric Junction
;
Hernia, Hiatal*
;
Humans
;
Infant, Newborn
;
Parturition*
;
Radiography
;
Thorax
;
Transient Tachypnea of the Newborn
9.Episodic Central Neurogenic Hyperventilation in an Awake Patient with Unilateral Pontine Infarction.
Ji Man LEE ; Jung Il KIM ; Woo Hyun CHEON ; Doo Kyo JUNG ; Sung Pa PARK ; Chung Kyu SUH
Journal of the Korean Neurological Association 2003;21(4):408-411
Central neurogenic hyperventilation (CNH) is characterized by sustained tachypnea inspite of an elevated arterial PaO2, pH and a low arterial PaCO2. CNH is common in patients with brainstem injury accompanied by a decreased level of consciousness but this also has been described in some alert patients with an invasive brainstem tumor. We report one case with CNH resulting from a unilateral pontine infarction. His consciousness was clear, and CNH spontaneously disappeared without any medication.
Brain Stem
;
Brain Stem Neoplasms
;
Consciousness
;
Humans
;
Hydrogen-Ion Concentration
;
Hyperventilation*
;
Infarction*
;
Tachypnea
10.A Case of Joubert Syndrome Associated with Nephrocalcinosis and Agenesis of Cerebellar Vermis.
Ji Hee KIM ; Hye Kyung SHIN ; Kee Hwan YOO ; Young Sook HONG ; Joo Won LEE ; Soon Kyum KIM
Journal of the Korean Society of Pediatric Nephrology 2002;6(2):266-273
There are several diseases characterized by neurologic abnormalities and renal disease. Joubert syndrome is one of them. Joubert syndrome is a relatively rare autosomal recessive syndrome. The most significant and constant neurologic finding is hypoplasia of the cerebellar vermis. Joubert syndrome is associated with hypotonia, retinal dystrophy, abnormal eye movement, delayed development, abnormal respiratory pattern (neonatal episodic tachypnea or apnea) and nephronophthisis. We report a boy with Joubert syndrome associated with nephrocalcinosis and agenesis of the cerebellar vermis. This patient had also abnormal eye movement, hypotonia, abnormal respiratory pattern, delayed development and chronic renal failure.
Eye Movements
;
Humans
;
Kidney Failure, Chronic
;
Male
;
Muscle Hypotonia
;
Nephrocalcinosis*
;
Neurologic Manifestations
;
Retinal Dystrophies
;
Tachypnea