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Skip to main content. Log In Sign Up. Terjemahan jurnal kejang demam. This sign dngan believed to be an adaptive mechanism, developed with the purpose of stimulating the immune system and preserving cell membrane integrity in the presence of threats. Although there is broad disagreement in the literature concerning normal body temperature in children, normal axillary temperature is fehris considered to range between C in the afternoon.
Any values above this range should be regarded as abnormal.
The correlation between fever and epileptic seizure is strong and has been well-established for dengaan. When treating the child with fever and epileptic seizure, the clinician may actually be faced with at least four distinct patient subgroups: Finally, the fourth group comprises patients in whom onset of fever occurred post- ictally; these cases are extraordinarily difficult to distinguish from actual febrile seizure, particularly in children presenting with low-grade fever and early in the course of the episode.
The objective of this review of the literature is to summarize current knowledge on febrile seizures and recent denhan – tions on ank of this condition. Definition and overview In the anaak conceptually outdated but still widely cited Consensus Development Meeting on Long-Term Management of Febrile Seizuresfebrile seizure was defined as follows: Febrile seizures are to be distinguished from epilepsy, which is characterized by recurrent non-febrile seizures.
An important aspect of febrile seizure is that it will always occur during the course of an infectious disease that does not affect the central nervous system.
Viral infections are more commonly associated than bacterial ones, most likely due to the higher incidence of the former in clinical practice. This review summarizes the current evidence and recommendations for diagnosis and management of patients with febrile seizures K ey words: The etiology and pathogenesis of febrile seizures have yet to be fully elucidated, particularly at the molecular level.
However, some environmental aspects are already understood and believed to be essential to development of the condition.
The underlying cause of the infectious process does not appear to be a determining factor of febrile seizures. The presence of fever is of course essential, even though its mechanism of action is unknown. Febrile seizures are also most common in the first day of fever, and correlate more with peak temperature than with speed of onset. Genetic aspects have been clearly established in the etio – logy and pathogenesis of febrile seizures. A history of febrile seizures in first-degree relatives is common, and concordance rates of febrile seizures are much higher in monozygotic than in dizygotic twin pairs.
Reports in the literature have described a connection between febrile seizures and various chromosomes, including 2q, 5q, 5, 8q, and 19, which appear to be associated with changes in neuronal sodium channel function. These studies are still incipient, however, and there is no single gene or well- defined inheritance pattern associated with febrile seizures. One of the most remarkable characteristics of febrile seizures is the fact that they occur only in a well-defined age range.
Although the immature brain is more susceptible to epileptic seizures, febrile convulsions cannot be ascribed to this factor alone, and the reasons behind the age-dependent nature of this condition even though it rarely occurs outside specific age ranges remains unclear. Natural history of the disease The clinical course of febrile seizures is quite well unders – tood. Seizures are usually generalized tonic-clonic, hypotonic, or clonic, short-lasting, and produce mild post-ictal manifestations.
Occasionally, febrile seizures are focal, prolonged, or lead to neurological signs in the post-ictal period; these are known as complex febrile seizures. Table 1 shows the characte – ristics of simple and complex febrile seizures, which has major implications for the clinical course and prognosis of children presenting with this condition. Complex febrile seizures are associated with higher odds of recurrence; furthermore, the differential diagnosis of epilepsy or acute symptomatic seizure must be pursued more rigorously in these cases.
Overall, febrile seizures are benign, and children who have had them show no significant difference in intelligence, head circumference growth, or behavior when compared with children with no history of the condition. Several factors have been described as increasing the odds of a first febrile seizure, such as fever grade, delayed development, delayed discharge from maternity care, and stay at daycare faci – lities.
However, the main risk factor appears to be family history of febrile seizures.
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The odds of recurrence also decrease over time. The key factors for recurrence are early age at first seizure, family history of febrile seizures, temperature inversely proportional to gradeand duration of febrile illness the shorter the febrile period, the higher the odds of recurrence. Finally, it bears stressing that a relationship however poorly understood exists between febrile seizures in childhood and development of temporal lobe epilepsy in adulthood.
InMaher and McLachlan studied families with febrile seizures and reported an association with mesial temporal sclerosis, a frequent cause of AED-refractory symptomatic focal epilepsy 7,10, Diagnosis The diagnosis of febrile seizure is essentially clinical.
Episodes should always be classified into simple or dengna febrile seizure. In children with complex seizures, other differential diagnoses such as focal denga or new-onset acute symptomatic seizure must always be considered, despite their rarity.
Lumbar puncture is indicated in children 18 months or younger with clinical signs suggesting meningitis or in parti – cularly severe presentations. Blood glucose measurement is essential, and any further laboratory testing should be requested as necessary according to clinical condition and diagnostic hypothesis.
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Electroencephalography may show changes in various cases, and is therefore of no practical use. Neuroimaging is also of little value in the diagnosis of febrile seizures.
The main differential diagnosis is CNS infection. Management Management of febrile seizures may be divided into acute treatment, prophylaxis, and aanak teaching. Acute care of the febrile seizure should be as for any epileptic seizure.
General principles of emergency care, such as dengsn – ment with the ABCs airway, breathing, and circulationshould precede administration of any specific drugs. Furthermore, most seizures cease spontaneously prior to arrival at the emergency department, and the clinician will often assess a child in the post-ictal state. Benzodiazepines fdbris the abortive treatment of choice: The prophylactic treatment of febrile seizures is highly contro – versial, and is the source of extensive discussion in the literature: When should these patients be treated?
Which is the best treatment option? Most children with febrile seizures fwbris have a single lifetime episode; seizures will recur in the rest.
Risk of recurrence is highest in patients with age less than 18 months at first seizure, family history of febrile seizures, and onset of fever less than one hour prior to the first seizure. If the child has one or more feebris these risk factors, prophylaxis may be considered. Several authors oppose prophylactic treatment of febrile seizures, arguing that they are a benign condition, that treatment does not alter prognosis, and that adverse effects can be a signi – ficant concern even in intermittent febria.
However, we find such a stance practically impossible to adopt in the Brazilian reality, mostly due to parental and psycholo – gical issues associated with epileptic seizures. Another argument in favor of prophylaxis is that the abrupt onset of seizure may lead to trauma, and that xengan seizures may sometimes progress to status epilepticus. The current consensus in the literature is that prophylaxis of simple febrile seizures carries no benefit. Conversely, prophylaxis for complex febrile seizures, is still febis, and available data are unconvincing.
However early and effective, antipyretic therapy does not prevent seizure recurrence. Both paracetamol and NSAIDs have been tested in double-blind randomized controlled trials and showed no benefit. It bears noting that seizure prophylaxis does not preclude general pediatric care for the underlying condition, and any other relevant measures, askeep as antipyretics or anti – biotic therapy, should be continued.
However, continuous prophylaxis is now exceedingly rare, due to the unfavorable side effect profile of both phenobarbital drowsiness, hyperactivity, learning difficulties and valproic acid weight gain, nausea, ppada loss, liver injury 7, We choose to begin continuous prophylaxis only in cases in which onset of fever was so dengah as to prevent the mother or care – giver from noticing it, and high temperature was only detected after the seizure.
Other indications supported by the literature include failure of intermittent prophylaxis and any case in which the initial febrile seizure progressed to status epilepticus. Such cases are fortunately rare, and use of continuous prophylaxis is increasingly rare. Currently, the most widely accepted regimen when the choice for prophylactic treatment is made is intermittent therapy with benzodiazepines.
This class of drugs is inexpensive, associated anakk good compliance, and provide excellent outcomes in terms of seizure prevention. The following weight- based dosages can be prescribed: Parent teaching should focus on the benign nature of the condition, mentioning the possibility paad recurrence and the slight increase in risk of developing epilepsy, but always stressing the importance of letting the child lead a normal life.
Parents should also receive guidance on responding to a seizure. Finally, parents should be informed of the association between immunization and febrile seizures, but encou – raged to vaccinate their children nonetheless. Clinical obser – vation for 48 hours after DTP vaccination and seven to ten days after measles vaccination is recommended. Although a great deal is known about the natural history and prognosis of these events, the need for prophylaxis and the best choice of prophylaxis are still the subject of much discussion.
Nonetheless, these episodes are a source of substantial suffering for pxda, their families and caregivers. Secondary prophylaxis after simple febrile seizures is unsup – ported by the current literature, but intermittent prophylaxis may be considered after complex seizures, especially in the event of protracted episodes or focal seizures.
The choice of whether to institute prophylaxis, and of the optimal regimen for prophylaxis when it is indeed chosen, will require not only a knowledge of the evidence but also an understanding of individual aspects of the patient, of his or her family, ffebris of the social structure of which the child is a part.
No conflicts of interest declared concer – ning the publication of this article. Lopez Deengan, Laurentys-Medeiros J, editor. Livraria e Editora Revinter; The prevalence and incidence of convulsive disorders in children.
Tratamento das crises febris. Guidelines for epidemiological studies on epilepsy.
askep febris – PDF Free Download
Inherited dengwn of childhood. Assessment of febrile seizures in children. Febrile convulsions in a national cohort followed up from birth. Risk factors for a first denvan seizure: Prognosis in children with febrile seizures. Predictors of recurrent febrile seizures: Is seizure duration the most important predictor of temporal lobe epilepsy? Epileptic seizures and epilepsies in children. Dam Meditor. A practical approach to epilepsy. Treatment of febrile seizures: Antipyretic agents for preventing recurrences of febrile seizures: