Objectives To evaluate the demographics, risk factors, correlation between carbon monoxide (CO) level and clinical findings, and laboratory findings determining the prognosis and ischemic myocardial injury due to CO intoxication in patients admitted to pediatric emergency department. Materials and Methods Six hundred seventy-four patients were admitted with CO intoxication between May 2007 and October 2009, 288 patients who required hospitalization were enrolled into the study prospectively. Results Incidentally, 144 (50%) of the patients were evenly distributed as girls and boys. Their age ranged between 7 months and 17 years; mean age was 8.6 years. The mean CO level was 26.8. The high levels were detected regarding lactate in 199 (90.1%) patients, creatine kinase (CK)-MB in 130 (45.1%) patients, CK in 80 (27.8%) patients, cardiac Troponin I in 35 (17.2%) patients, and lactate dehydrogenase in 34 (15.7%) patients. There was a significant positive correlation when symptoms like syncope, loss of consciousness, and convulsion were compared with carboxyhemoglobin, lactate, CK, CK-MB, and lactate dehydrogenase levels (P < 0.05), whereas there was no correlation when compared with cardiac Troponin I (P > 0.05). To determine the accuracy of predicting severe CO intoxication, sensitivity of 52.6% and specificity of 85.7% were found in receiver operating characteristic analysis when the lactate level was 3.85 mmol/L, whereas sensitivity of 70.5% and specificity of 59.6% were found when the carboxyhemoglobin level was 27.1%. One hundred forty-six (%50.8) of the patients had normal electrocardiographic findings, whereas 135 (46.8%) had sinus tachycardia, 6 (2%) had right branch block, and 1 (0.34%) had atrioventricular block. In 34 patients who had high CK-MB and Troponin I levels, only sinus tachycardia was detected in electrocardiography, and there were no ST changes. Hyperbaric oxygen was necessary in 2 patients admitted with coma. Conclusions In children admitted because of CO intoxication, the blood lactate levels may give more accurate information in terms of loss of consciousness and convulsion, lactate level could be taken as a measure of severe poisoning and may help to decide for hyperbaric oxygen treatment.

Background: The aim of the research is to determine the etiology and clinical features of seizures in critically ill children admitted to a pediatric intensive care unit (PICU).

To determine the indication and necessity of echocardiographic assessment and therapeutic interventions in critically ill children. A total of 140 children, including 75 mechanically ventilated (MV) and 65 spontaneously breathing (SB) children, who were admitted consecutively from March to August 2013 were evaluated prospectively. Data regarding the indication for echocardiography and therapeutic approaches used were documented. For evaluating disease severity, the Pediatric Risk of Mortality Score III (PRISM) was ascertained. The correlation between PRISM score and the requirement of echocardiographic evaluations were analyzed. Patients ages were between 45 days to 18 years. The male-to-female ratio was 1.33. In 35.4% patients who underwent echocardiographic evaluation, no definitive alteration occurred in treatment approach, whereas in the remaining 64.6% patients, decisive or supplemental information was gathered. Echocardiography was indicated in 88% MV children and 46.2% SB children. Echocardiographic evaluation was necessary in MV children and there was a positive correlation between the PRISM score and the requirement of echocardiographic assessment (p<0.001). Echocardiographic evaluation is an invaluable tool especially in MV children and the requirement of echocardiographic assessment increases according to clinical severity. Basic training for intensivists in this procedure is crucial and needs to be improved and supported in critically ill.

Pediatric palliative care (PPC) is an evolving field that focuses on supporting children with life-limiting conditions, where the quality of care is vital. This study is a retrospective observational investigation that examines the experiences of caregivers to inform health and social service planning and enhance PPC quality. Methods: Data of pediatric patients aged 3 months to 18 years admitted to a PPC inpatient unit over two years were retrospectively reviewed. Sociodemographic characteristics of primary caregivers, including age, gender, number of siblings, education, income, occupation, and marital status, were recorded. Caregiver burden and burnout were assessed using the Zarit Burden Interview and the Maslach Burnout Inventory, respectively. Associations between caregiver characteristics and these measures were analyzed. Results: A total of 118 patients and caregivers were evaluated; 54.2% of patients were male. The most common diagnoses were neurological diseases (44.9%), followed by syndromic–genetic disorders (28.8%). About 34% of patients required more than three medical devices. Most caregivers were female (91.5%), mainly mothers and 53% had only primary education. No significant differences in care burden or burnout were found based on caregiver gender, marital status, or child’s diagnosis. However, the use of nasogastric tubes and multiple medical devices was associated with higher burnout. Lower income was significantly linked to higher care burden, while longer caregiving duration correlated with both increased burden and burnout. A moderate positive correlation was found between Zarit and Maslach scores. Conclusions: The complexity of PPC patients’ care increases caregiver burden and burnout. Expanding specialized PPC services is crucial to support caregivers and sustain home-based care.

The problem of EOL care of a child is very important because the recovery of a family from grief over a child’s death depends on that manner. For improving the quality of this specific care, it would be useful to assess the life expectancy/survival of congenital anomalies, life-threatening diseases, conditions that may shorten a child’s life, and the outcomes of palliative care units regarding mortality. Besides, there is an urgent need for more data on what families define as ‘good death’ and how to cope with the loss. Not only caregivers but also siblings, grandparents, relatives, and healthcare professionals are impacted by a child’s death and their needs must be explored. Pediatric palliative care staff in low/middle-income countries need educational assistance for skills of multidisciplinary training about end-of-life care to improve appropriate care for dying children and their families. It is important to provide sensitive and empathetic end-of-life care to children in a family-centered manner helping them to find comfort, meaning, and support while enhancing the quality of a child’s life and death. Many attending physicians felt inexperienced when communicating with dying patients and their families while discussing the transition to palliative care and resuscitation status. Also, the good death of a child is an emerging concept in this research domain to improve end-of-life care for dying children and their families. The goal of this review was to provide pediatric healthcare professionals and physicians with an overview of palliative care regarding end-of-life issues.