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1.
J Crit Care ; 27(5): 474-9, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22591573

ABSTRACT

PURPOSE: The aims of this study were to determine the prevalence of hypophosphatemia and to discuss the clinical implications of hypophosphatemia in critically ill children. MATERIALS AND METHODS: A retrospective review of the medical records of children admitted to the pediatric intensive care unit from December 2006 to December 2007 was conducted. RESULTS: In 60.2% (n = 71) of the patients, any serum phosphorous level at admission and at the third day or seventh day after admission to pediatric intensive care unit was in hypophosphatemic range. Sepsis was present in 22.9% (n = 27) of the children studied and was associated with hypophosphatemia (P = .02). Hypophosphatemia was also associated with use of furosemide (P = .04), use of steroid (P = .04), use of ß(2) agonist (P = .026), and use of an H(2) blocker (P = .004). There was a significant association between hypophosphatemia and the rate to attain target caloric requirements by enteral route (P = .007). The median time to attain target caloric requirements by enteral route was 2.9 ± 1.9 (0.2-10) days in the normophosphatemic group and 4.4 ± 2.8 (0.3-12) days in the hypophosphatemic group. In the multiple regression model, solely the rate to attain the target caloric requirements by enteral route demonstrated independent association with hypophosphatemia (P = .006; ß = .27; 95% confidence interval, 0.02-0.09). Significant association was found between hypophosphatemia and the duration of mechanical ventilation and between hypophosphatemia and pediatric intensive care unit length of stay (P = .02 and P = .001, respectively). CONCLUSIONS: Critically ill pediatric patients are prone to hypophosphatemia, especially if they cannot be fed early by enteral route. Hypophosphatemia is associated with an increased duration of mechanical ventilation and increased length of stay in the pediatric intensive care unit, suggesting that active repletion might improve these parameters.


Subject(s)
Critical Illness , Hypophosphatemia/epidemiology , Intensive Care Units, Pediatric/statistics & numerical data , Adolescent , Child , Child, Preschool , Comorbidity , Female , Humans , Hypophosphatemia/mortality , Infant , Infant, Newborn , Length of Stay/statistics & numerical data , Male , Parenteral Nutrition/statistics & numerical data , Prevalence , Respiration, Artificial/statistics & numerical data , Retrospective Studies
2.
Turk J Pediatr ; 51(3): 271-4, 2009.
Article in English | MEDLINE | ID: mdl-19817271

ABSTRACT

Over the past decade, tuberculosis has been recognized worldwide as a public health problem of increasing proportions. We report a patient who presented with epistaxis and generalized petechiae. The diagnosis was immune thrombocytopenia and the patient was treated with intravenous immunoglobulin and pulse steroid. The bleeding continued and thrombocyte level was low despite therapy. Chest X-ray and a computed tomography scan of the thorax showed right upper lobe opacities and bilateral interstitial infiltrates. The patient also had a history of close contact with an individual with active tuberculosis. The thrombocytopenia was resistant to standard therapy, but resolved after antituberculosis treatment. This report is the first case of a child with immune thrombocytopenia secondary to pulmonary tuberculosis.


Subject(s)
Purpura, Thrombocytopenic, Idiopathic/complications , Tuberculosis, Pulmonary/complications , Antitubercular Agents/therapeutic use , Child, Preschool , Glucocorticoids/administration & dosage , Humans , Immunoglobulins/administration & dosage , Infusions, Intravenous , Isoniazid/therapeutic use , Male , Platelet Count , Pulse Therapy, Drug , Purpura, Thrombocytopenic, Idiopathic/diagnosis , Purpura, Thrombocytopenic, Idiopathic/drug therapy , Pyrazinamide/therapeutic use , Rifampin/therapeutic use , Tomography, X-Ray Computed , Tuberculosis, Pulmonary/diagnosis , Tuberculosis, Pulmonary/drug therapy
4.
Pediatr Int ; 50(1): 35-9, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18279202

ABSTRACT

BACKGROUND: Convulsive status epilepticus (CSE) may end fatally or leave serious sequelae. CSE treatment, invariably an emergency case, is based upon i.v. benzodiazepines as well as phenytoin, barbiturates or both. The present paper reports efficiency of lidocaine in CSE. METHODS: The effects of lidocaine on patients with CSE due to infectious and non-infectious reasons were compared. Lidocaine was given in 29 episodes of CSE to 49 patients having failed to respond to first-line anticonvulsive drugs, such as diazepam, phenobarbital and phenytoin therapy. Lidocaine was given in doses of 2 mg/kg bolus i.v., and then in 4 mg/kg per h infusion. RESULTS: Mean duration of lidocaine infusion was 14.6 +/- 7.8 h. Effectiveness of lidocaine in patients with CSE was found to be 44.4%. Also, 11 patients responded to a single dose of lidocaine (37.9%), while another two (6.9%) required another dose to suppress their seizures. Patients with seizures attributable to infections were observed to have responded favorably to lidocaine when compared to those with seizures due to epilepsy (37.9% vs 6.8%; P < 0.05). Subsequent epilepsy was found to occur more frequently in patients with a poor response to lidocaine than in patients with a good response (P < 0.05). Adverse reactions to lidocaine were observed in three patients (10.3%), two of them having ventricular arrhythmia. As for the other patient, the focal seizure developed into a generalized one. CONCLUSIONS: Lidocaine seems to be useful for the management of CSE as a rapid-acting anticonvulsant, particularly in patients with CSE due to infections. But further studies with larger number of patients are needed.


Subject(s)
Anticonvulsants/therapeutic use , Lidocaine/therapeutic use , Status Epilepticus/drug therapy , Anticonvulsants/administration & dosage , Child, Preschool , Female , Humans , Lidocaine/administration & dosage , Male
5.
Pediatr Emerg Care ; 23(5): 314-7, 2007 May.
Article in English | MEDLINE | ID: mdl-17505274

ABSTRACT

Colchicine poisoning is an uncommon, but potentially life-threatening, toxicologic emergency. The clinical features associated with overdose and the options for treatment are discussed. Colchicine poisoning typically shows 3 phases: initially, gastrointestinal symptoms predominate; in the second phase, multiorgan failure may occur, possibly leading to death. If the patient survives, the third phase of recovery follows, during which the patient often presents with hair loss. Early fatality is due to cardiovascular collapse and respiratory failure; however, pancytopenia and overwhelming septicemia can occur later. All patients suspected of having colchicine intoxication because of its unpredictable outcome should be managed according to the principles of intensive care, irrespective of the actual degree of poisoning. In those patients who survive the initial phase of poisoning, filgrastim (granulocyte colony-stimulating factor) offers an effective method of treating pancytopenia and preventing overwhelming septicemia. Daily monitoring of the patients' hematological status is strongly recommended. We are reporting a case of previously healthy girl who developed a multisystem organ failure after colchicine intoxication. The patient recovered completely and had no residual outcome.


Subject(s)
Colchicine/poisoning , Multiple Organ Failure/chemically induced , Acute Disease , Alopecia/chemically induced , Ataxia/chemically induced , Blood Transfusion , Case Management , Child, Preschool , Combined Modality Therapy , Disseminated Intravascular Coagulation/chemically induced , Disseminated Intravascular Coagulation/drug therapy , Dobutamine/therapeutic use , Female , Fluid Therapy , Furosemide/therapeutic use , Gastroenteritis/chemically induced , Humans , Hyponatremia/chemically induced , Hyponatremia/complications , Hypotension/chemically induced , Multiple Organ Failure/drug therapy , Multiple Organ Failure/therapy , Pancytopenia/chemically induced , Pancytopenia/therapy , Phenytoin/adverse effects , Phenytoin/therapeutic use , Poisoning/blood , Poisoning/drug therapy , Poisoning/therapy , Seizures/drug therapy , Seizures/etiology
6.
Pediatr Nephrol ; 22(5): 715-9, 2007 May.
Article in English | MEDLINE | ID: mdl-17146668

ABSTRACT

Continuous renal replacement therapy (CRRT) has become an important supportive therapy for critically ill children with acute renal failure. In Turkey, commercially available diafiltration and replacement fluids cannot be found on the market. Instead, peritoneal dialysis fluids for dialysis and normal saline as replacement fluid are used. The first objective of this study was to examine metabolic complications due to CRRT treatments. The second objective was to determine demographic characteristics and outcomes of patients who receive CRRT. We did a retrospective chart review of all pediatric patients treated with CRRT between February and December 2004. Thirteen patients received CRRT; seven survived (53.8%). All patients were treated with continuous venovenous hemodiafiltration. Median patient age was 71.8 +/- 78.8 (1.5-180) months. Hyperglycemia occurred in 76.9% (n=10), and metabolic acidosis occurred in 53.8% (n=7) of patients. Median age was younger (48.8 vs.106.2 months), median urea level (106.2 vs. 71 mg/dl) and percent fluid overload (FO) (17.2% vs. 7.6%, respectively) were higher, and CRRT initiation time was longer (8.6 vs 5.6 days) in nonsurvivors vs. survivors for all patients, although these were not statistically significant. CRRT was stopped in all survivors, and four nonsurvivors (67%) were on renal replacement therapy at the time of death. Hyperglycemia and metabolic acidosis were frequently seen in CRRT patients when commercially available diafiltration fluids were not available. Using peritoneal dialysis fluid as dialysate is not a preferable solution. Early initiation of CRRT offered survival benefits to critically ill pediatric patients. Mortality was associated with the primary disease diagnosis.


Subject(s)
Acute Kidney Injury/therapy , Glomerular Filtration Rate , Hemofiltration/adverse effects , Metabolic Diseases/etiology , Acidosis/epidemiology , Acute Kidney Injury/mortality , Bicarbonates/therapeutic use , Child , Fluid Therapy/adverse effects , Humans , Hyperglycemia/etiology , Insulin/therapeutic use , Multiple Organ Failure/etiology , Retrospective Studies , Survival Analysis , Treatment Outcome
7.
Pediatr Int ; 48(6): 582-5, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17168978

ABSTRACT

BACKGROUND: The aim of this study was to examine the characteristics of seizure due to poisoning. METHODS: This was a retrospective analysis, throughout 4 years of hospital admissions for poisoning. Data of patients with seizures due to poisoning were evaluated with respect to the causes, frequencies and complications of seizures. RESULTS: Among the 1561 admissions due to intoxication during the review period, seizures developed in 26 cases (1.6%). Tricyclic antidepressant overdose (n = 11, 42%) was the leading cause of seizure due to poisoning. Generalized tonic-clonic seizures were observed in 24 patients. Status epilepticus developed in six patients (23%). Mechanical ventilation was applied in 12 (46%) patients. Cardiac complications were observed in 11 (42%) patients with seizures. Two patients who had cardiac arrest due to acepromazine maleate and imipramine intoxication died. CONCLUSION: One of the causes of seizures in pediatric age group is intoxication. Seizures due to intoxications may cause serious clinical conditions. Intoxications should be thought when a patient is admitted with the diagnosis of afebrile seizure even if there is no history of drug intake.


Subject(s)
Antidepressive Agents, Tricyclic/poisoning , Seizures/chemically induced , Seizures/epidemiology , Child , Child, Preschool , Female , Humans , Incidence , Infant , Male , Medical Records , Retrospective Studies , Seizures/mortality , Seizures/therapy , Survival Analysis , Turkey/epidemiology
8.
Ulus Travma Acil Cerrahi Derg ; 10(3): 168-72, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15286887

ABSTRACT

BACKGROUND: This study was designed to evaluate the current situation of interhospital transport of pediatric patients requiring emergent care. METHODS: Using a clinical prospective and multicenter design, 1,666 interhospital transports of pediatric patients were evaluated in 18 centers. Non-emergency transports and newborn transports were not included, so 854 transports were eligible for evaluation. Data were collected by means of a comprehensive form filled by a physician at the receiving hospital. RESULTS: The physicians who gave the decisions for the transports were pediatricians in 60%, general physicians in 15.4%, and residents in 6%, while no identification existed in 159 transports (18.6%). The receiving hospitals were not notified prior to the transport in 79.3%. Pretransport information about the patients were adequate in 26.1% and inadequate in 31.8%; no information was available in 42.1%. Ambulances were used in 64.4% of the transports, of which only 16.2% was fully equipped. Unqualified or inexperienced personnel were in charge in 42.8% of the transports. In 26.3% of the transports, the patients arrived at the receiving hospital in an agonized state. CONCLUSION: It appears that there are no established guidelines for the emergency transport of pediatric children in Turkey.


Subject(s)
Ambulances , Emergency Medical Services/statistics & numerical data , Patient Transfer/statistics & numerical data , Transportation of Patients/statistics & numerical data , Adolescent , Child , Child, Preschool , Critical Illness , Humans , Infant , Pediatrics , Prospective Studies , Turkey/epidemiology
9.
Pediatr Int ; 44(1): 83-6, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11982878

ABSTRACT

BACKGROUND: It is critical to establish a safe and functional i.v. access in severely sick patients. We evaluated the frequency of application and complications of central venous catheters in a pediatric intensive care unit. METHODS: Pediatric patients in whom central venous catheters were inserted between March 1997 and May 1999 in the Pediatric Emergency Room and Intensive Care Unit were enrolled in this study. Patients were evaluated with respect to age, sex, weight, central venous catheter indication, site, duration of catheter stay and complications. RESULTS: During the study period a total of 156 central venous catheters were successfully inserted into 146 patients. Of the 156 central venous catheter attempts, 148 (94.9%) were placed into the subclavian vein, six were inserted into the femoral vein, and two into the jugular vein. In 156 attempts, arterial injuries occurred in 20 cases (12.8%). Pneumothorax developed in two patients on mechanical ventilation. Three catheters had to be removed due to catheter related infections. The mortality rate was 0%. CONCLUSIONS: We concluded that subclavian central venous catheterization is a safe procedure with minimal complications in pediatric patients. Arterial injury was the most frequent complication. In experienced hands, the success rate was 100%. Subclavian central venous catheter insertion may be considered as the first approach in critically ill patients.


Subject(s)
Catheterization, Central Venous/methods , Adolescent , Catheterization, Central Venous/adverse effects , Child , Child, Preschool , Critical Illness/therapy , Humans , Infant , Infant, Newborn , Intensive Care Units, Pediatric , Subclavian Vein
10.
Turk J Pediatr ; 44(1): 54-7, 2002.
Article in English | MEDLINE | ID: mdl-11858381

ABSTRACT

Acute isoniazid (INH) poisoning is uncommon in children. Although most physicians are aware of INH hepatotoxicity, acute INH poisoning and its treatment are not well recognized. INH is increasingly being used to control the spread of tuberculosis, and physicians should know its potentially fatal effects. INH overdose is known to result in rapid onset of seizures, metabolic acidosis and prolonged obtundation. We report two cases of obtundation secondary to INH overdose that was immediately reversed by pyridoxine. Parenteral pyridoxine administration is an effective method in INH intoxication. The intravenous form of pyridoxine must be available in the emergency care units, and INH toxicity should be suspected in any patient with refractory seizures and metabolic acidosis.


Subject(s)
Antitubercular Agents/poisoning , Epilepsy, Tonic-Clonic/chemically induced , Isoniazid/poisoning , Seizures/chemically induced , Adolescent , Drug Overdose , Female , Humans , Infant , Male , Pyridoxine/therapeutic use
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