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Fonte: Global Strategy for dengue prevention and control, 2012-2020 , OMS.
Scenario
The emergence and diffusion of all dengue serotypes from Asia to America, Africa, and Eastern regions of the Mediterranean represent a threat of pandemics.
3
Alarm and shock signs of dengue fever are not routinely researched.
Health professionals have not been using the clinical staging prescribed by the Ministry of Health (MoH). Patient hydration levels were lower than those prescribed by the handbook.
Laboratorial tests, such as blood cell count, which are necessary for the proper hydration and platelets dosage, were not solicited in the recommended frequency.
Test results took longer than they should for the appropriate care of patients with dengue fever. The type of assistance (supervised) and the gap between reassessments were lower than the established by the Ministry of Health. Conclusion: the high levels of mortality are correlated with the nonfollowing of technical rules for the diagnosis and treatment of cases of dengue fever, as established by the MoH
Dengue
Dengue fever is a dynamic and systemic disease. The proper care depends on the early recognition of the alarm signs, the continued monitoring, the restaging of cases (dynamic and continued) and the prompt water reposition.
Alarm Signs: intense and continued abdominal pain, persistent vomiting, postural hypotension and/or lipothymy, painful hepatomegaly, mucosal bleeding or important hemorrhages (hematemesis and/or melena), drowsiness and/or irritability, decrease of diuresis, sudden decrease of body temperature or hypothermia, sudden increase of hematocrit, sudden drop of platelet count and breathing discomfort.
The determinant factor of the severe forms of dengue fever are the vascular endothelial alterations, with plasmatic leakage, which leads to shock, expressed by hemoconcentration, hypoalbuminnemy and/or cavity spillage.
Laboratorial exams (complete blood count) and specific exams for dengue fever.
Treatment Follow-up plan
HIPTESE DIAGNSTICA CASO SUSPEITO
Notification
Histria Clnica
EXAME FSICO
Dengue
Warning: The complete blood count (CBC) is mainly used to assess the hematocrit, to identify hemoconcentration. Hemoconcentration indicates the likely alteration of capillary permeability (plasmatic leakage), associated with severity, as well as defining the need for hydration and response to instituted reposition therapy.
In dengue fever, the leukogram is variable (leucopenia may indicate another viral infection and leukocytosis does not eliminate the disease); Thrombocytopenia does not necessarily constitute a risk factor to bleeding in patients with suspected dengue fever, but the progressive decrease in platelet count indicates the need for closer monitoring, for it indicates the patient may suffer complications, which will be considered an alarm sign.
Dengue - CBC
Hematocrit One hematocrit at the beginning of the feverish phase establishes the personal basal value of the patient; From first through third day - generally normal; Rising hematocrit: establishes the beginning of the Critical Phase; The value is directly proportional to the severity; An increase of the hematocrit, compared to the prior result, is highly suggestive of an evolution to the critical phase of the disease, with plasma leakage.
Hct Children
Women
Men
> 44 %
> 50%
IMMUNE RESOPONSE
MICROENVIRONMENT OF CYTOTOXINS GENETIC FACTORS
Unregulated Response
SEVERE CASES
Immune Response
DEATH 9
HEALING
5 6
Reabsorption
Dehydration
Shock Bleeding
Organic Damage
Feverish
Critical
Recovery
10
Group B
Group C
Presenceof ofone oneor ormore morealarm alarmsigns signs Bleedingpresent presentor ornot. not. Presence . .Bleeding Nohypotension. hypotension. No
Group D
13
Post Exam
Grupo C
Presence of one or more alarm signs. Presence or not of spontaneous bleeding. No hypotension
a) Antiemetic, paracetamol or dypirone and at home rehydration. b) Supervised oral rehydration of 80ml/Kg/day, of which 1/3 in 4 hours. Keep in observation bed, with clinical and hematocrit reassessment 4 hours after hydration c) Volume replacement: 20ml/Kg/day in 1 hour with saline. Monitoring in hospital bed. Clinical and hematocrit reassessment every 2 hours. Repeat expansion phase up to 03 phases if there is no improvement in hematocrit (hemoconcentration) and clinical parameters. d) IV hydration: 20ml/Kg in 20 minutes. ICU bed. Repeat this phase up to 3 times. Clinical reassessment every 15-30 minutes and hematocrit after 2 hours.
Post-exam