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PTI Category: Health & Medicine (/category/HealthMedicine) | Oct 17, 2017 AdChoices
Fatty Liver Treatment Doc PTI Patient Care Treatment for Lupus
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Fatty Liver Treatment
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Description 1. TROMBOCITOPENIA asociado al EMBARAZO Pedro García Lázaro Hematólogo clínico HNAAA Chiclayo,10 de julio del 2007 2. TROMBOCITOPENIA Y EMBARAZO:EPIDEMIOLOGIA…
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1. TROMBOCITOPENIA asociado al EMBARAZO Pedro García Lázaro Hematólogo clínico HNAAA Chiclayo,10 de julio del 2007 2. TROMBOCITOPENIA Y EMBARAZO:EPIDEMIOLOGIA
- Estudios prospectivos (nivell evidencia III): plaquetas 120,000-150,000/ul no son incomunes III-trimestre
- Afecta al 7% de todos los embarazos
- 1357 embarazadas-parto a término:
- Intervalo confianza 95%:109,000-341,000
3. DIAGNOSTICO DIFERENCIAL
- Isolated thrombocytopenia
- Type IIb von Willebrand disease
- Thrombocytopenia associated with systemic disorders
- HELLP (hemolysis, elevated liver function tests, low platelets syndrome)
4. DIAGNOSTICO DIFERENCIAL
- Thrombotic microangiopathies:
- Thrombotic thrombocytopenic purpura (PTT)
- Hemolytic uremic syndrome (SUH)
- Systemic lupus erythematosus (LES)
- Antiphospholipid antibodies (SAF)
- Disseminated intravascular coagulation (CID)
- Viral infection (human immunodeficiency virus [HIV],EpsteinBarr
- virus [EBV], cytomegalovirus [CMV])
5. GUIA PTI-2003
- GUIDELINES FOR THE INVESTIGATION AND MANAGEMENT OF IDIOPATHIC
- THROMBOCYTOPENIC PURPURA IN ADULTS, CHILDREN AND IN PREGNANCY
- British Journal of Haematology, 2003, 120, 574–596
6. NIVELES DE EVIDENCIA
- Ia Evidence obtained from meta-analysis of randomized controlled trials
- Ib Evidence obtained from at least one randomized controlled trial
- IIa Evidence obtained from at least one well-designed controlled study without randomization
- IIb Evidence obtained from at least one other type of welldesigned quasi-experimental study*
- III Evidence obtained from well-designed non-experimental descriptive studies, such as comparative studies, correlated studies and case studies
- IV Evidence obtained from expert committee reports or opinions and ⁄ or clinical experience of respected authorities
7. GRADOS DE RECOMENDACIÓN
- A Requires at least one r andomized controlled trial as part of a body of literature of overall good quality and consistency addressing specific recommendation
- B Requires the availability of well-conducted clinical studies but no randomized clinical trials on the topic of recommendation
- Evidence levels IIa, IIb, III
8.
- C Requires evidence obtained from expert committee reports or opinions and ⁄ or clinical experiences of respected authorities. Indicates an absence of directly applicable clinical studies of good quality
9. LABORATORIO:PLAQUETAS75% todos los casos trombocitopenia –embarazo
- Patogenesis:Efectos de hemodilución o depuración acelerada de plaquetas x mecanismos inmunes o no inmunes.
- trombocitopenia leve (raro < 80,000/ul)
- Gestantes saludables con resto cuentas sanguíneas normales
- Ocurre comúnmente en III trimestre
- Plaquetas normales antes y después del embarazo
- No se asocia con hemorragia materna
11.
- No se asocia con hemorragia fetal o neonatal
- Trombocitopenia Gestacional es díficil distinguir de PTI:
- cuando trombocitopenia es identificada por primera vez durante embarazo
- cuentas previas de plaquetas:no están documentadas, no historia previa de PTI
- Cuidado obstétrico estandar
- Parto con analgesia epidural si lo requiere
12. Púrpura trombocitopénica inmune
- Causa mas común de trombocitopenia significativa en I trimestre
- 5% de casos de trombocitopenia-embarazo
- Anticuerpos contra glicoproteínas plaquetarias GPIIb/IIIa y GP Ib/IX
- Depuración de estas plaquetas cubiertas por Ig-G x RES
13. PTI: DIAGNÓSTICO
- Diagnóstico por exclusión
- Historia previa de trombocitopenia
- Trombocitopenia moderada a severa: 20 x 109 ⁄ l do not need treatment until delivery is imminent
- Platelet counts >50 x 109 ⁄ l are safe for normal vaginal delivery in patients with otherwise normal coagulation
- Platelet counts > 80 x 109 ⁄ l are safe for caesarean section, spinal or epidural anaesthesia in patients with otherwise normal coagulation
16. Recommendation: (All Grade C)
- In women who need treatment , both oral
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