Body mass index and blood uric acid level were found to be the two independent factors to distinguish between different types of metabolic syndrome.
To investigate the value of chest ultrasound in the diagnosis of pneumonia in adults.

The prospective observational cohort study was conducted at Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey, from December 1, 2015,to March 1, 2016, and comprised suspected pneumonia patients aged >18 years. Sonographic pneumonia was defined as lung consolidation with air bronchograms. Treating clinicians were blinded to lung ultrasound results. All patients who were advised to undergo thoracic computerised tomography after physical examination were subjected to posteroanterior chest X-ray before the scan. Patients in whom pneumonia was detected in the scan underwent thorax ulstasonography according to Bedside Lung Ultrasound in Emergency protocol. Follow-up was done with medical record review to obtain the final diagnosis and antibiotic usage. Data was analysed using SPSS 22.

Of the 125 patients, 61(48.8%) were male. The overall mean age was 73.9±14.6 years. In 97(77.6%) patients, pneumominal infiltration was detected by thorax ultrasound, and in 57(45.6%) the infiltration was detected with chest X-ray.

Thorax ultrasound was found to be a helpful diagnostic method when performed according to the Bedside Lung Ultrasound in Emergency protocol.
Thorax ultrasound was found to be a helpful diagnostic method when performed according to the Bedside Lung Ultrasound in Emergency protocol.
The current study was planned to investigate the relationship of serum level of pentraxine-3 with various clinical and neurological scales and scores.

The prospective case-control study was conducted at the Emergency Department of the Ondokuz Mayis University, Samsun, Turkey, from March 2013 to June 2014, and comprised subarachnoid haemorrhage patients and healthy. Pentraxine-3levels were measured from serum samples and compared with sub-groups of the various scales and scores used in the study. Data was analysed using SPSS 15.

Of the 77 subjects, 40(52%) were patients and 37(48%) were controls. Pentraxine-3levels in the cases were significantly higher than the controls (p<0.001). Among the cases, pentraxine-3level of the Glasgow Coma Scale sub-group was significantly different between the severe and mild categories (p=0.048). https://www.selleckchem.com/products/obeticholic-acid.html Likewise, pentraxine-3 levels were significantly different in terms of Fisher scale in patients with minor haemorrhage compared to those with massive haemorrhage (p=0.026). Also, pentraxine-3 levels were significantly higher in patients who died compared to those who fully recovered (p=0.042).

There was found to be a relationship between pentraxine-3 level and the clinical severity of subarachnoid haemorrhage patients.
There was found to be a relationship between pentraxine-3 level and the clinical severity of subarachnoid haemorrhage patients.
To determine the clinicopathological pattern of childhood malignancies registered with a pathology-based tumour registry.

The descriptive retrospective study was conducted at the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, and comprised data related to all the histologically diagnosed malignant childhood tumours in the institutional tumour registry from January 2009 to December 2018. Data was analysed using SPSS 20 for the site of involvement, age distribution and histological types of tumours.

Of the total 37793 malignant tumours, 1279(3.38%) were in paediatric subjects aged <15 years. There were 820(64.1%) male subjects and 459(35.8%) were female. Lymph node malignancies were the commonest 261(20.4%), followed by eye tumours 251(19.6%), and brain 107(8.3%).

Lymphomas and eye tumours were found to form the main bulk of childhood cancer.
Lymphomas and eye tumours were found to form the main bulk of childhood cancer.
To determine the clinical, haematological and genetic factors responsible for variable phenotypes of sickle haemoglobin, sickle haemoglobin-beta, and beta-thalassemia patients.

The study was conducted in Bannu, Lakki, Tank and Dera Ismail Khan districts of Khyber Pakhtunkhwa province of Pakistan from September 2016 to November 2017, and comprised sickle haemoglobin, sickle haemoglobin-beta, and beta-thalassemia patients. Clinical, haematological and genetic determinants were evaluated using haemoglobin electrophoresis and allele-specific primers through polymerase chain reaction to determine alpha and beta thalassemia, and CgT substitution at position -158 (referred to as Xmn-I polymorphism) in gamma-globin gene. Data was analysed using SPSS 20.

Eight b-thalassemia mutations were identified that included IVS I-5(G C), codon 8/9 (+G), codon 30 (G C), -88 (C T), Cap+1(A G), codon 41/42 (-TCTT), IVS I-1(G T) and codon 16(-C). Codon 30 (G C) and -88 (C T) were found only in Pashtoon subjects, Cap+1(A G) and IVS I-1(G T) in Balochi subjects, while 75% of IVS I-5(G C) mutation cases were found in Punjabi ethnic group. In the Pashtoon group, 13 sickle haemoglobin homozygous patients were identified for the first time. Both alpha thalassemia and Xmn-I polymorphism in homozygous condition were common among those with mild phenotype.

Phenotypic expression of sickle haemoglobin beta thalassemia was found to be extremely variable and alpha thalassemia and Xmn-I polymorphism in homozygous condition were found to be additional genetic modifiers of the disease.
Phenotypic expression of sickle haemoglobin beta thalassemia was found to be extremely variable and alpha thalassemia and Xmn-I polymorphism in homozygous condition were found to be additional genetic modifiers of the disease.
To measure the impact of intermittent kangaroo mother care on weight-gain of neonates in a neonatal intensive care unit.

The randomised controlled trial was conducted at the Department of Neonatology, the Children Hospital and the Institute of Child Health, Lahore, Pakistan, from March to October, 2018, and recruited newborns admitted to the neonatal intensive care unit. The subjects were randomised into case and control groups. Intermittent kangaroo mother care was given in the case group for seven days. Data was collected and analysed using SPSS 23.

Of the 153 neonates, 140(91.5%) were included; 70(50%) in each group. The most common reason for admission was bronchopneumonia 49(35%). In the case group, average weight gain was 10.22±1.65 grams/kg/day compared to 7.87±1.71 in the control group (p=0.0001). The average length of stay in the case group was significantly low compared to the control group (p=0.003). Multivariate analysis determined the effect of kangaroo mother care therapy as effective (p<0.
Body mass index and blood uric acid level were found to be the two independent factors to distinguish between different types of metabolic syndrome. To investigate the value of chest ultrasound in the diagnosis of pneumonia in adults. The prospective observational cohort study was conducted at Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey, from December 1, 2015,to March 1, 2016, and comprised suspected pneumonia patients aged >18 years. Sonographic pneumonia was defined as lung consolidation with air bronchograms. Treating clinicians were blinded to lung ultrasound results. All patients who were advised to undergo thoracic computerised tomography after physical examination were subjected to posteroanterior chest X-ray before the scan. Patients in whom pneumonia was detected in the scan underwent thorax ulstasonography according to Bedside Lung Ultrasound in Emergency protocol. Follow-up was done with medical record review to obtain the final diagnosis and antibiotic usage. Data was analysed using SPSS 22. Of the 125 patients, 61(48.8%) were male. The overall mean age was 73.9±14.6 years. In 97(77.6%) patients, pneumominal infiltration was detected by thorax ultrasound, and in 57(45.6%) the infiltration was detected with chest X-ray. Thorax ultrasound was found to be a helpful diagnostic method when performed according to the Bedside Lung Ultrasound in Emergency protocol. Thorax ultrasound was found to be a helpful diagnostic method when performed according to the Bedside Lung Ultrasound in Emergency protocol. The current study was planned to investigate the relationship of serum level of pentraxine-3 with various clinical and neurological scales and scores. The prospective case-control study was conducted at the Emergency Department of the Ondokuz Mayis University, Samsun, Turkey, from March 2013 to June 2014, and comprised subarachnoid haemorrhage patients and healthy. Pentraxine-3levels were measured from serum samples and compared with sub-groups of the various scales and scores used in the study. Data was analysed using SPSS 15. Of the 77 subjects, 40(52%) were patients and 37(48%) were controls. Pentraxine-3levels in the cases were significantly higher than the controls (p<0.001). Among the cases, pentraxine-3level of the Glasgow Coma Scale sub-group was significantly different between the severe and mild categories (p=0.048). https://www.selleckchem.com/products/obeticholic-acid.html Likewise, pentraxine-3 levels were significantly different in terms of Fisher scale in patients with minor haemorrhage compared to those with massive haemorrhage (p=0.026). Also, pentraxine-3 levels were significantly higher in patients who died compared to those who fully recovered (p=0.042). There was found to be a relationship between pentraxine-3 level and the clinical severity of subarachnoid haemorrhage patients. There was found to be a relationship between pentraxine-3 level and the clinical severity of subarachnoid haemorrhage patients. To determine the clinicopathological pattern of childhood malignancies registered with a pathology-based tumour registry. The descriptive retrospective study was conducted at the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, and comprised data related to all the histologically diagnosed malignant childhood tumours in the institutional tumour registry from January 2009 to December 2018. Data was analysed using SPSS 20 for the site of involvement, age distribution and histological types of tumours. Of the total 37793 malignant tumours, 1279(3.38%) were in paediatric subjects aged <15 years. There were 820(64.1%) male subjects and 459(35.8%) were female. Lymph node malignancies were the commonest 261(20.4%), followed by eye tumours 251(19.6%), and brain 107(8.3%). Lymphomas and eye tumours were found to form the main bulk of childhood cancer. Lymphomas and eye tumours were found to form the main bulk of childhood cancer. To determine the clinical, haematological and genetic factors responsible for variable phenotypes of sickle haemoglobin, sickle haemoglobin-beta, and beta-thalassemia patients. The study was conducted in Bannu, Lakki, Tank and Dera Ismail Khan districts of Khyber Pakhtunkhwa province of Pakistan from September 2016 to November 2017, and comprised sickle haemoglobin, sickle haemoglobin-beta, and beta-thalassemia patients. Clinical, haematological and genetic determinants were evaluated using haemoglobin electrophoresis and allele-specific primers through polymerase chain reaction to determine alpha and beta thalassemia, and CgT substitution at position -158 (referred to as Xmn-I polymorphism) in gamma-globin gene. Data was analysed using SPSS 20. Eight b-thalassemia mutations were identified that included IVS I-5(G C), codon 8/9 (+G), codon 30 (G C), -88 (C T), Cap+1(A G), codon 41/42 (-TCTT), IVS I-1(G T) and codon 16(-C). Codon 30 (G C) and -88 (C T) were found only in Pashtoon subjects, Cap+1(A G) and IVS I-1(G T) in Balochi subjects, while 75% of IVS I-5(G C) mutation cases were found in Punjabi ethnic group. In the Pashtoon group, 13 sickle haemoglobin homozygous patients were identified for the first time. Both alpha thalassemia and Xmn-I polymorphism in homozygous condition were common among those with mild phenotype. Phenotypic expression of sickle haemoglobin beta thalassemia was found to be extremely variable and alpha thalassemia and Xmn-I polymorphism in homozygous condition were found to be additional genetic modifiers of the disease. Phenotypic expression of sickle haemoglobin beta thalassemia was found to be extremely variable and alpha thalassemia and Xmn-I polymorphism in homozygous condition were found to be additional genetic modifiers of the disease. To measure the impact of intermittent kangaroo mother care on weight-gain of neonates in a neonatal intensive care unit. The randomised controlled trial was conducted at the Department of Neonatology, the Children Hospital and the Institute of Child Health, Lahore, Pakistan, from March to October, 2018, and recruited newborns admitted to the neonatal intensive care unit. The subjects were randomised into case and control groups. Intermittent kangaroo mother care was given in the case group for seven days. Data was collected and analysed using SPSS 23. Of the 153 neonates, 140(91.5%) were included; 70(50%) in each group. The most common reason for admission was bronchopneumonia 49(35%). In the case group, average weight gain was 10.22±1.65 grams/kg/day compared to 7.87±1.71 in the control group (p=0.0001). The average length of stay in the case group was significantly low compared to the control group (p=0.003). Multivariate analysis determined the effect of kangaroo mother care therapy as effective (p<0.
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