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1.
Allergy, Asthma & Respiratory Disease ; : 51-56, 2019.
Article in Korean | WPRIM | ID: wpr-719520

ABSTRACT

PURPOSE: Noninvasive positive pressure ventilation (NIPPV) is one of the ventilation-supporting methods by providing adequate exogenous pressure without intubation or tracheostomy. We aimed to assess the frequency and clinical factors for pneumothorax occurring during NIPPV application in a tertiary children's hospital. METHODS: We selected cases of pneumothorax related to NIPPV by keyword searching in our institution's clinical data warehouse, and their medical records were retrospectively reviewed. RESULTS: During a period of 17 years, 15 cases undergoing NIPPV developed pneumothorax, which was an incidence of 0.64% (15 of 2,343). There were 9 neonates and 6 adolescents. In 9 neonates, pneumothorax was caused by the continuous positive airway pressure (CPAP) ventilator, and occurred on 2 days after birth (median, range 1–3 days). In neonates, pneumothorax developed within 36 hours after CPAP application. One neonate underwent tracheal intubation and 3 neonates underwent chest tube insertion. In the postteenager group, pneumothorax developed 23 months (median, range 5 days to 47 months) after NIPPV application with a mask. All of the 6 patients had underlying neuromuscular disorders and one had superimposed interstitial lung disease. One of the 7 cases underwent surgical treatment and 4 cases were intubated. One case died from the deterioration of underlying interstitial lung disease. CONCLUSION: Although it rarely happens, the NIPPV can result in pneumothorax. In most cases, it can be resolved by supportive cares with oxygen or chest tube with or without tracheostomy. The prognosis is related to the type of underlying disease and its progression.


Subject(s)
Adolescent , Humans , Infant, Newborn , Chest Tubes , Continuous Positive Airway Pressure , Incidence , Intubation , Lung Diseases, Interstitial , Masks , Medical Records , Noninvasive Ventilation , Oxygen , Parturition , Pneumothorax , Positive-Pressure Respiration , Prognosis , Respiratory Insufficiency , Retrospective Studies , Tracheostomy , Ventilators, Mechanical
2.
Allergy, Asthma & Respiratory Disease ; : 206-211, 2019.
Article in Korean | WPRIM | ID: wpr-762200

ABSTRACT

PURPOSE: To evaluate clinical characteristics of pediatric nontraumaitc chylothorax and to suggest appropriate therapeutic managements. METHODS: We retrospectively reviewed medical records of 22 patients with nontraumatic chylothorax from January 2005 to December 2018 in the Children's Hospital of Seoul National University. We analyze their etiology, treatment, complications and outcome. RESULTS: Of the 22 patients, 16 were diagnosed before 1 year old and 6 after 1 year old. The causes of chylothorax under 1-year-old children were related to congenital factors (n=9), unknown causes (n=5), and high central venous pressure (n=2). The causes of chylothorax over 1-year-old children were related to congenital factors (n=3), unknown causes (n=1), high venous pressure (n=1), and lymphoma (n=1). All patients had dietary modification. Eight of them were cured by dietary modification, but there was no improvement in over 1-year-old children. Medication was added to patients refractory to dietary modification. Four patients with medication were improved and 5 were improved by surgical management. Nutritional, immunological and other complications occurred in many patients. Five death cases were reported. Four patients were under 1 year old and 1 was over 1 year old. The causes of nontraumatic chylothorax in dead patients were high central venous pressure (n=3), congenital (n=1), and unknown (n=1). CONCLUSION: Nontraumatic chylothorax more frequently occurs in under 1-year-old children. The most common cause is congenital factors. Stepwise management is effective in many patients, but specific treatment is needed in some cases. The prognosis is related to the onset of age and underlying diseases.


Subject(s)
Child , Humans , Central Venous Pressure , Chylothorax , Diet , Feeding Behavior , Lymphoma , Medical Records , Pediatrics , Prognosis , Retrospective Studies , Seoul , Venous Pressure
3.
Obstetrics & Gynecology Science ; : 112-116, 2015.
Article in English | WPRIM | ID: wpr-36576

ABSTRACT

OBJECTIVE: The hereditary nonpolyposis colorectal cancer is inherited syndrome characterized by the development of cancers in various organ system; these includes colorectum, endometrium, and less frequently, small bowel, stomach, urinary tract, ovaries, and brain. We aimed to investigate the clinicopathologic characteristics of hereditary nonpolyposis colorectal cancer patients who had both endometrial and colorectal cancers. METHODS: Between January 2004 and December 2013, 12 women diagnosed with endometrial and colorectal cancers in a single institution were included in this analysis. For these patients, clinical and molecular findings were analyzed retrospectively. RESULTS: All 12 women undertook microsatellite instability analysis, and 9 (75%) were confirmed of having microsatellite instability-high. Among 9 cases with immunohistochemical staining for MLH1 and MSH2, 6 were positive for the loss of mismatch repair protein. Mutational analyses for MLH1 and MSH2 were performed in 3 out of 12 patients; all of them showed germline mutation. CONCLUSION: This study suggests that there is a genetic background in patients with double primary malignancies in their endometrium and colorectum when analyzed with microsatellite instability studies, immunohistochemistry staining, and mutation studies. This finding supports the necessity of re-defining the high-risk groups in endometrial cancers clinically. This will also help diagnose malignancies in such patients in early stages, as well as counsel other family members.


Subject(s)
Female , Humans , Brain , Colorectal Neoplasms , Colorectal Neoplasms, Hereditary Nonpolyposis , DNA Mismatch Repair , Endometrial Neoplasms , Endometrium , Germ-Line Mutation , Immunohistochemistry , Microsatellite Instability , Microsatellite Repeats , Ovary , Retrospective Studies , Stomach , Urinary Tract
4.
Obstetrics & Gynecology Science ; : 59-64, 2015.
Article in English | WPRIM | ID: wpr-221362

ABSTRACT

OBJECTIVE: This study aimed to compare perioperative and postoperative morbidity of older and younger women undergoing sacrocolpopexy (SCP). METHODS: A retrospective study included 271 patients who underwent laparotomic SCP for symptomatic pelvic organ prolapse from November 2008 to June 2013 at our institution. By the review of medical records, perioperative and postoperative data including the length of the surgery, estimated blood loss, blood transfusion, the length of hospital stay, wound complications and febrile morbidity were collected. In addition, cardiovascular, pulmonary, gastrointestinal, genitourinary, or neurological adverse events were retrieved. The need for an indwelling urinary catheter or performance of clean intermittent self-catheterization, mesh erosion rate and the number of days required for each were included in the postoperative outcomes. For the outcome variable analyzed in this study, the patients was dichomotized into women aged 65 and older and those younger than 65. RESULTS: One hundred and thirty-five (49.8%) patients were younger than 65 and 136 (50.2%) were aged 65 and older. Older women had higher body mass index, vaginal parity and prior surgery for hysterectomy than younger women (P<0.05). And older women had higher baseline comorbidities, such as hypertension, diabetes, cardiac disease (P<0.05), and their American society of Anesthesiologist class was higher (P<0.001). In the perioperative and postoperative complication, older group showed no differences in most of the operation-related complication rates, but gastrointestinal complication rate. Also, mesh erosion rate was not found to be significantly different between the two groups at the last visit. CONCLUSION: Older women undergoing laparotomic SCP have similar perioperative and postoperative morbidities as younger women, suggesting surgeons can counsel older and younger women similarly in terms of operative risks.


Subject(s)
Female , Humans , Blood Transfusion , Body Mass Index , Comorbidity , Heart Diseases , Hypertension , Hysterectomy , Length of Stay , Medical Records , Parity , Pelvic Organ Prolapse , Postoperative Complications , Retrospective Studies , Urinary Catheters , Wounds and Injuries
5.
Journal of Korean Medical Science ; : 1152-1159, 2010.
Article in English | WPRIM | ID: wpr-187254

ABSTRACT

Promoter CpG island hypermethylation has become recognized as an important mechanism for inactivating tumor suppressor genes or tumor-related genes in human cancers of various tissues. Gene inactivation in association with promoter CpG island hypermethylation has been reported to be four times more frequent than genetic changes in human colorectal cancers. Hepatocellular carcinoma is also one of the human cancer types in which aberrant promoter CpG island hypermethylation is frequently found. However, the number of genes identified to date as hypermethylated for hepatocellular carcinoma (HCC) is fewer than that for colorectal cancer or gastric cancer, which can be attributed to fewer attempts to perform genome-wide methylation profiling for HCC. In the present study, we used bead-array technology and coupled methylation-specific PCR to identify new genes showing cancer-specific methylation in HCC. Twenty-four new genes have been identified as hypermethylated at their promoter CpG island loci in a cancer-specific manner. Of these, TNFRSF10C, HOXA9, NPY, and IRF5 were frequently hypermethylated in hepatocellular carcinoma tissue samples and their methylation was found to be closely associated with inactivation of gene expression. Further study will be required to elucidate the clinicopathological implications of these newly found DNA methylation markers in hepatocellular carcinoma.


Subject(s)
Humans , Antimetabolites, Antineoplastic/therapeutic use , Azacitidine/analogs & derivatives , Carcinoma, Hepatocellular/drug therapy , Cell Line, Tumor , CpG Islands , DNA Methylation , GPI-Linked Proteins/genetics , Gene Expression Profiling , Homeodomain Proteins/genetics , Interferon Regulatory Factors/genetics , Liver Neoplasms/drug therapy , Neuropeptide Y/genetics , Oligonucleotide Array Sequence Analysis , Promoter Regions, Genetic , Tumor Necrosis Factor Decoy Receptors/genetics
6.
Korean Journal of Anesthesiology ; : 283-288, 1995.
Article in Korean | WPRIM | ID: wpr-61009

ABSTRACT

The clinical complex of ARDS includes hypoxemia, hypercapnia, diffuse pulmonary infiltrates on chest radiograph, and depressed pulmonary compliance. Even with improved intensive care, the onset of severe disease with ARDS is associated with high mortality rate of 55% to 85% in an adult population. The etiology of ARDS remains uncertain, although increasing experimental evidence suggests that high inflation pressures may be involved in the pulmonary injury that is associated with ARDS. The use of low volume, pressure limited mechanical ventilation with permissive hypercapnia has been proposed to reduce the mortality rates associated with severe ARDS. Pressure-controlled ventilation has been proposed to recruit closed alveolar units and improve oxygenation through changing the inspiratory flow pattern from a square wave as used with volume-controlled ventilation to a rapidly exponentially decaying curve and through maintaining airway pressure at a constant level throughout the inspiratory phase. We present the case of a severe ARDS patient in whom a specific ventilatory management strategy of low peak inflation pressures and permissive hypercapnia appears to have favorably influenced survival and warrants further clinical evaluation.


Subject(s)
Adult , Humans , Hypoxia , Compliance , Hypercapnia , Inflation, Economic , Critical Care , Lung Injury , Mortality , Oxygen , Radiography, Thoracic , Respiration, Artificial , Respiratory Distress Syndrome , Ventilation
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