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Demam Berdarah Dengue
Diagnosa dan Penatalaksanaan
KURNIA F. JAMIL
Sub-Bagian Penyakit Tropik & Infeksi,
Bagian Ilmu Penyakit Dalam
FK-UNSYIAH/RSUZA
BANDA ACEH
2007
Demam Berdarah Dengue
Masih merupakan masalah penyakit infeksi yang serius
di Indonesia
DEPKES-RI tahun 2005
Jumlah kasus 80.837 dengan 1.099 kematian
Ledakan kasus 5 tahunan
Sejak tahun 1968 dan seterusnya
Self Limiting Diseases
Pendahuluan
 Virus dengue termasuk
genus Flavivirus dari
family Flaviviridae
 Ada 4 serotipe: Den 1- 4
 Patogenesis masih
kontroversi
 Penelitian masih
diperlukan
Overview of the Major Viral Hemorrhagic Fever
Family Genus Mortality Transmission
Cook GC, Zumla A. Manson’s Tropical Diseases, 2003
Arenaviridae Lassa West Africa 16% Rodents
Junin’58* Argentina 30% Rodents
Machupo’63 Bolivia 25% Rodents
Sabia’90 Brazil 30% Rodents
Guanarito’90 Venezuela 25% Rodents
Flaviviridae Dengue 1-4 0.2-2% Mosquitos
Yellow fever virus * 10-85% Mosquitos
Kyasanur * India 5% Ticks
Omsk Rusia 2% Ticks
Bunyaviridae Phlebovirus- Rift Valley HF 1% Mosquitos
Hantavirus - HF Renal Synd * 5-15% Rodents
Nairovirus- Crimean Congo HF 20-50% Ticks
Puumala 1% Rodents
Filoviridae Marburg ** 20-25% Monkey
Ebola ** 70-90% Monkey
Alphaviridae Chikungunya # 0% Mosquitos
Reoviridae Coltvirus <1% Ticks
* Cardiac complication
** Nosocomial # Mild HF
Replication and Transmission
of Dengue Virus (Part 1)
1. Virus transmitted
to human in mosquito
saliva
2. Virus replicates
in target organs
3. Virus infects white
blood cells and
lymphatic tissues
4. Virus released and
circulates in blood
3
4
1
2
Patogenesis DBD
 Teori virulensi
virus
 Teori infection
enhancing
antibody
Viral Risk Factors
for DBD Pathogenesis
 Virus strain (genotype)
– Epidemic potential: viremia level, infectivity
 Virus serotype
– DBD risk is greatest for DEN-3, followed by
DEN-2, DEN-1 and DEN-4
Hypothesis on Pathogenesis
of DHF (Part 1)
 Persons who have experienced a dengue
infection develop serum antibodies that can
neutralize the dengue virus of that same
(homologous) serotype
Neutralizing antibody to Dengue 1 virus
Dengue 1 virus
Homologous Antibodies Form
Non-infectious Complexes
Non-neutralizing antibody
Complex formed by neutralizing antibody and virus
Hypothesis on Pathogenesis
of DHF (Part 2)
 In a subsequent infection, the pre-existing
heterologous antibodies form complexes
with the new infecting virus serotype, but
do not neutralize the new virus
Non-neutralizing antibody to Dengue 1 virus
Dengue 2 virus
Heterologous Antibodies Form
Infectious Complexes
Complex formed by non-neutralizing antibody
and virus
Hypothesis on Pathogenesis
of DHF (Part 3)
 Antibody-dependent enhancement is the
process in which certain strains of dengue
virus, complexed with non-neutralizing
antibodies, can enter a greater proportion
of cells of the mononuclear lineage, thus
increasing virus production
Heterologous Complexes Enter More
Monocytes, Where Virus Replicates
Non-neutralizing antibody
Dengue 2 virus
Complex formed by non-neutralizing
antibody and Dengue 2 virus
Hypothesis on Pathogenesis
of DHF (Part 4)
 Infected monocytes release vasoactive
mediators, resulting in increased vascular
permeability and hemorrhagic
manifestations that characterize DHF and
DSS
Replikasi
2 – 3 hari
Sirkulasi & Jaringan
Infeksi : Macrofag
Monosit
Limfosit
ANTIBODI
Trombosit
Kompleks
Ag-Ab
•Trombosit dihancurkan
•Agregasi terganggu
Perdarahan
Demam
Permeabilitas
Kapiler
Mediator
SSD
Sitokin
Menstimulasi
Sistem Koagulasi
Fibrinogen
Faktor V,VII,
VIII,X,XII
Perdarahan
KID
Temp
Trombosit
Bifasik
DEMAM &
TROMBOSITOPENIA
Kompleks Imun
Manifestations of dengue infection
Dengue virus infection
Asymptomatic Symptomatic
Undifferentiated
fever
Dengue fever
syndrome
Without
haemorrhage
With unusual
haemorrhage
Dengue
haemorrhagic
fever
No shock Dengue shock
syndrome
Dengue
fever
Dengue
haemorrhagic fever
Non-specific constitutional symptoms observed
in haemorrhagic fever patients with dengue
Criteria DHF(%)
Injected pharynx 96.8
Vomiting 57.9
Constipation 53.5
Abdominal pain 50.0
Headache 44.6
Generalized lymphadenopathy 40.5
Conjunctival injection 32.8
Cough 21.5
Rhinitis 12.8
Maculopapular rash 12.1
Myalgia/arthralgia 12.0
Enanthema 8.3
Abnormal reflex 6.7
Diarrhea 6.4
Palpable spleen 6.3
Coma 3.0
The following classifications are proposed :
• Probable-an acute febrile illness with two or more of
the following manifestations :
– headache
– retro-orbital pain
– myalgia
– arthralgia
– rash
– haemorrhagic manifestations
– leukopenia
– serology (+) or DF occurrence at the same location /
time
Kriteria Diagnosis DBD (WHO 1997)
•Demam, atau riwayat demam akut, antara 2-7 hari biasanya bifasik,
•Trombositopenia (< 100.000/mm3)
•Terdapat minimal satu dari manifestasi perdarahan berikut ini:
Uji tourniquet positif
Petekie, ekimosis, atau purpura
Perdarahan mukosa, saluran cerna, bekas suntikan atau di tempat lain
Hematemesis atau melena
•Terdapat minimal satu dari tanda-tanda plasma leakage oleh karena
peningkatan permeabilitas kapiler berikut:
Hematokrit meningkat > 20% dibandingkan hematokrit
rata-rata pada usia, jenis kelamin, dan populasi yang sama
Hematokrit turun hingga > 20% dari hematokrit awal,
setelah pemberian cairan
Terdapat efusi pleura, asites , hiponatremia,
hipoalbuminemia
I VIV VII VIIIIIIII IV
36 oC
39 oC
40 oC
38 oC
37 oC
Pola panas Demam Dengue
Ruam primer Ruam sekunder
Warning Signs for Dengue Shock
When Patients Develop
DSS:
• 3 to 6 days after onset of
symptoms
Initial Warning Signals:
• Disappearance of fever
• Drop in platelets
• Increase in hematocrit
Alarm Signals:
• Severe abdominal pain
• Prolonged vomiting
• Abrupt change from fever
to hypothermia
• Change in level of
consciousness (irritability
or somnolence)
Four Criteria for DHF:
• Fever
• Hemorrhagic manifestations
• Excessive capillary
permeability
• 100,000/mm3 platelets
CENTERS FOR DISEASE CONTROL
AND PREVENTION
Four Grades of DHF
 Grade 1
• Fever and nonspecific constitutional symptoms
• Positive tourniquet test is only hemorrhagic manifestation
 Grade 2
• Grade 1 manifestations + spontaneous bleeding
 Grade 3
• Signs of circulatory failure (rapid/weak pulse, narrow
pulse pressure, hypotension, cold/clammy skin)
 Grade 4
• Profound shock (undetectable pulse and BP)
CENTERS FOR DISEASE CONTROL
AND PREVENTION
Problem in Dengue Fever/Dengue
Hemorrhagic Fever in Indonesia
 High viral transmission
 Economical impact :
Cost of treatment
Lost of productivity
 Mortality especially in children about 2 %
 Not effective prevention:
vector eradication
no effective vaccine
CENTERS FOR DISEASE CONTROL
AND PREVENTION
years
1996
1994
1992
1990
1988
1986
1984
1982
1980
1978
1976
1974
1972
1970
1968
70000
60000
50000
40000
30000
20000
10000
0
Incidence of Dengue Hemorrhagic Fever
in Indonesia 1968-1996
Ministry of Health, Rep of Indonesia
CENTERS FOR DISEASE CONTROL
AND PREVENTION
years
1996
1994
1992
1990
1988
1986
1984
1982
1980
1978
1976
1974
1972
1970
1968
50
40
30
20
10
0
Mortality of Dengue Hemorrhagic Fever
in Indonesia 1968-1997
Ministry of Health, Rep of Indonesia
Treatment of Dengue
Haemorrhagic Fever
 Fluids
 Rest
 Antipyretics (avoid aspirin and non-steroidal
anti-inflammatory drugs)
 Monitor blood pressure, hematocrit, platelet
count, level of consciousness
Tatalaksana DBD pada Dewasa
Protokol 1
Penanganan Tersangka ( Probable ) DD/DBD dewasa tanpa syok
Protokol 2
Pemberian cairan pada tersangka DBD dewasa di ruang rawat
Protokol 3
Penatalaksanaan DBD dengan peningkatan Ht > 20 %
Protokol 4
Penatalaksanaan Perdarahan Spontan pada DBD dewasa
Protokol 5
Tatalaksana sindroma syok Dengue pada dewasa
Keluhan DBD
(Kriteria WHO 1997)
Hb, Ht Normal
Tromb > 100.000/mm³
Observasi
Rawat jalan
Periksa Hb, Ht dan
leuko, tromb/ 24 jam
Hb, Ht normal
Trombo < 100.000
Hb, Ht meningkat
Trombo N / turun
Protokol 1. Penanganan Tersangka
( Probable )
DD / DBD Dewasa tanpa syok
Rawat Inap
( Protokol 2 )
Protokol 2. Pemberian cairan pada tersangka DBD
dewasa di ruang rawat
Suspek DBD
Perdarahan Spontan dan Masif (-)
Syok (-)
Hb,Ht (n)
Tromb.
<100.000
Hb,Ht 10-20%
Tromb.
<100.000
Hb,Ht > 20%
Tromb.<100.00
0
◘Infus Kristaloid
◘Hb,Ht,Tromb.
tiap 24 jam
Infus Kristaloid
Hb,Ht,Tromb.
tiap 12 jam
Protokol 3
Volume cairan kristaloid per hari yang diperlukan :
1500 + 20 X ( BB dalam kg – 20 )
Contoh :
BB 50 kg : 1500 + 20 X ( 50 – 20)
= 1500 + (20 x 30)
= 1500 + 600
= 2100 ml
(Pan American Health Organization: Dengue and Dengue Hemorrhagic
Fever: Guidelines for Prevention and Control. PAHO:
Washington,D.C,1994:67).
Awasi kadar elektrolit darah jika memungkinkan.
Protokol 3. Penatalaksanaan DBD dengan peningkatan Ht > 20 %
5 % defisit cairan
Kristaloid 6 – 7 ml/kg/jam
PERBAIKAN TIDAK MEMBAIK
Kristaloid 5 ml/kg/jam Kristaloid 10 ml/kg/jam
TIDAK MEMBAIK
Kristaloid 15 ml/kg/jam
MEMBURUK  SYOK
PROTOKOL 4 / 5
PERBAIKAN
Kristaloid 3 ml/kg/jam
PERBAIKAN
STOP CAIRAN
PERBAIKAN
PERBAIKAN
3-4 jam
2 jam
3 jam
24-48 jam
Protokol 4.
Penatalaksanaan Perdarahan Spontan pada DBD dewasa
KASUS DBD :
Perdarahan Spontan dan Masif : - Epistaksis tidak terkendali
- Hematemesis melena
- Perdarahan otakSyok (-)
Hb, Ht, Trombo, Leuko, Pemeriksaan
Hemostasis (KID)
Golongan darah, uji cocok serasi
Transfusi komponen darah :
* PRC (Hb<10 g %)
* FFP (APTT > 1,5 X normal )
* TC (Tromb.<100.000)
* Pemantauan Hb, Ht, Tromb. Tiap 4-6 jam
* Ulang pemeriksaan hemostasis 24 jam kemudian
KID +:
HEPARINISASI
5000 – 10.000 / 24J
Protokol 5. Tatalaksana Syok pasien Dewasa
AIRWAY
BRAETHING : O2 1 – 4 l/menit
CIRCULATION : 10 – 20 ml/kgBB
20 – 30 MENITPERBAIKAN TETAP SYOK
Kristaloid 20-30 ml/kgBB
20-30 menit
TETAP SYOK
Ht k
Koloid 10-20 ml/kg/BB
tetes cepat 10-15 menit
Transfusi PRC
10 ml/kgBB
Ht k
TETAP SYOK
Koloid hingga
maksimal 30 ml/kgBB
TETAP
SYOK
Pasang CVP
Hipovolemik Normovolemik
KRISTALOID TETAP SYOK
Inotropik , Vasoaktif
Koreksi : As/Bs, Electr,Glikemia,
Anemia, KID, Infeksi Sekunder
PERBURUKAN
AIRWAY
BREATHING : O2 1 – 4 l/menit
CIRCULATION : 10 – 20 ml/kgBB
Protokol 5. Tatalaksana Syok pasien Dewasa
20 – 30 MNT
PERBAIKAN
Kristaloid
7 ml/kg/jam dalam
1 jam
PERBAIKAN
Kristaloid
5 ml/kg/jam dalam
1 jam
PERBAIKAN
Kristaloid
3 ml/kg/jam dalam
1 jam
STABIL 24 – 48 JAM
PERBURUKAN
TETAP SYOK
Protokol pemberian zat inotropik / zat vasoaktif
Dopamin
5 mg/kg/mnt dititrasikan sampai 10 mg/kg/mnt
Sasaran : MAP > 60 mmHg.
Gagal
Dobutamin 5 mg/kg/mnt + Norepinefrin 0,05 – 0,1 mg/kg/mnt
10 mg/kg/mnt 1 mg/kg/mnt
Epinefrin 0,1 mg/kg/mnt
Dititrasikan setiap 0,1 mg/kg/mnt
Max 2 mg/kg/mnt
GAGAL ?
Indikasi masuk ICU :
 Syok yang tidak dapat teratasi maksimal 2 jam
 Syok berulang
 Syok dengan perdarahan hebat
 Syok dengan penyulit seperti : kegagalan pernafasan,
ensefalopati, gagal jantung, dll.
Penatalaksanaan Sindrom Renjatan Dengue
Kriteria Pemulangan pasien DBD
1. Tidak demam selama 24 jam tanpa antipiretik
2. Nafsu makan membaik
3. Klinis tampak perbaikan
4. Hematokrit stabil
5. Tiga hari setelah renjatan teratasi
6. Jumlah trombosit > 50.000
7. Tidak dijumpai distres pernafasan
KESIMPULAN
 Indonesia merupakan negara tropis dengan risiko
kemungkinan terjadinya DBD cukup tinggi
 Menegakkan diagnosis serta penatalaksanaan
Dengue tidaklah mudah
 Penanganan pasien DBD melalui pedoman
tatalaksana yang ada, di sarana pelayanan kesehatan
 Pedoman ini perlu disosialisasikan ke semua petugas
kesehatan, pemantauan, evaluasi implementasinya
agar penanganan DBD dapat maksimal
THANK YOU

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Demam Berdarah Dengue

  • 1. Demam Berdarah Dengue Diagnosa dan Penatalaksanaan KURNIA F. JAMIL Sub-Bagian Penyakit Tropik & Infeksi, Bagian Ilmu Penyakit Dalam FK-UNSYIAH/RSUZA BANDA ACEH 2007
  • 2. Demam Berdarah Dengue Masih merupakan masalah penyakit infeksi yang serius di Indonesia DEPKES-RI tahun 2005 Jumlah kasus 80.837 dengan 1.099 kematian Ledakan kasus 5 tahunan Sejak tahun 1968 dan seterusnya Self Limiting Diseases
  • 3. Pendahuluan  Virus dengue termasuk genus Flavivirus dari family Flaviviridae  Ada 4 serotipe: Den 1- 4  Patogenesis masih kontroversi  Penelitian masih diperlukan
  • 4. Overview of the Major Viral Hemorrhagic Fever Family Genus Mortality Transmission Cook GC, Zumla A. Manson’s Tropical Diseases, 2003 Arenaviridae Lassa West Africa 16% Rodents Junin’58* Argentina 30% Rodents Machupo’63 Bolivia 25% Rodents Sabia’90 Brazil 30% Rodents Guanarito’90 Venezuela 25% Rodents Flaviviridae Dengue 1-4 0.2-2% Mosquitos Yellow fever virus * 10-85% Mosquitos Kyasanur * India 5% Ticks Omsk Rusia 2% Ticks Bunyaviridae Phlebovirus- Rift Valley HF 1% Mosquitos Hantavirus - HF Renal Synd * 5-15% Rodents Nairovirus- Crimean Congo HF 20-50% Ticks Puumala 1% Rodents Filoviridae Marburg ** 20-25% Monkey Ebola ** 70-90% Monkey Alphaviridae Chikungunya # 0% Mosquitos Reoviridae Coltvirus <1% Ticks * Cardiac complication ** Nosocomial # Mild HF
  • 5. Replication and Transmission of Dengue Virus (Part 1) 1. Virus transmitted to human in mosquito saliva 2. Virus replicates in target organs 3. Virus infects white blood cells and lymphatic tissues 4. Virus released and circulates in blood 3 4 1 2
  • 6. Patogenesis DBD  Teori virulensi virus  Teori infection enhancing antibody
  • 7. Viral Risk Factors for DBD Pathogenesis  Virus strain (genotype) – Epidemic potential: viremia level, infectivity  Virus serotype – DBD risk is greatest for DEN-3, followed by DEN-2, DEN-1 and DEN-4
  • 8. Hypothesis on Pathogenesis of DHF (Part 1)  Persons who have experienced a dengue infection develop serum antibodies that can neutralize the dengue virus of that same (homologous) serotype
  • 9. Neutralizing antibody to Dengue 1 virus Dengue 1 virus Homologous Antibodies Form Non-infectious Complexes Non-neutralizing antibody Complex formed by neutralizing antibody and virus
  • 10. Hypothesis on Pathogenesis of DHF (Part 2)  In a subsequent infection, the pre-existing heterologous antibodies form complexes with the new infecting virus serotype, but do not neutralize the new virus
  • 11. Non-neutralizing antibody to Dengue 1 virus Dengue 2 virus Heterologous Antibodies Form Infectious Complexes Complex formed by non-neutralizing antibody and virus
  • 12. Hypothesis on Pathogenesis of DHF (Part 3)  Antibody-dependent enhancement is the process in which certain strains of dengue virus, complexed with non-neutralizing antibodies, can enter a greater proportion of cells of the mononuclear lineage, thus increasing virus production
  • 13. Heterologous Complexes Enter More Monocytes, Where Virus Replicates Non-neutralizing antibody Dengue 2 virus Complex formed by non-neutralizing antibody and Dengue 2 virus
  • 14. Hypothesis on Pathogenesis of DHF (Part 4)  Infected monocytes release vasoactive mediators, resulting in increased vascular permeability and hemorrhagic manifestations that characterize DHF and DSS
  • 15.
  • 16. Replikasi 2 – 3 hari Sirkulasi & Jaringan Infeksi : Macrofag Monosit Limfosit ANTIBODI
  • 21.
  • 22. Manifestations of dengue infection Dengue virus infection Asymptomatic Symptomatic Undifferentiated fever Dengue fever syndrome Without haemorrhage With unusual haemorrhage Dengue haemorrhagic fever No shock Dengue shock syndrome Dengue fever Dengue haemorrhagic fever
  • 23. Non-specific constitutional symptoms observed in haemorrhagic fever patients with dengue Criteria DHF(%) Injected pharynx 96.8 Vomiting 57.9 Constipation 53.5 Abdominal pain 50.0 Headache 44.6 Generalized lymphadenopathy 40.5 Conjunctival injection 32.8 Cough 21.5 Rhinitis 12.8 Maculopapular rash 12.1 Myalgia/arthralgia 12.0 Enanthema 8.3 Abnormal reflex 6.7 Diarrhea 6.4 Palpable spleen 6.3 Coma 3.0
  • 24. The following classifications are proposed : • Probable-an acute febrile illness with two or more of the following manifestations : – headache – retro-orbital pain – myalgia – arthralgia – rash – haemorrhagic manifestations – leukopenia – serology (+) or DF occurrence at the same location / time
  • 25. Kriteria Diagnosis DBD (WHO 1997) •Demam, atau riwayat demam akut, antara 2-7 hari biasanya bifasik, •Trombositopenia (< 100.000/mm3) •Terdapat minimal satu dari manifestasi perdarahan berikut ini: Uji tourniquet positif Petekie, ekimosis, atau purpura Perdarahan mukosa, saluran cerna, bekas suntikan atau di tempat lain Hematemesis atau melena •Terdapat minimal satu dari tanda-tanda plasma leakage oleh karena peningkatan permeabilitas kapiler berikut: Hematokrit meningkat > 20% dibandingkan hematokrit rata-rata pada usia, jenis kelamin, dan populasi yang sama Hematokrit turun hingga > 20% dari hematokrit awal, setelah pemberian cairan Terdapat efusi pleura, asites , hiponatremia, hipoalbuminemia
  • 26. I VIV VII VIIIIIIII IV 36 oC 39 oC 40 oC 38 oC 37 oC Pola panas Demam Dengue Ruam primer Ruam sekunder
  • 27.
  • 28.
  • 29. Warning Signs for Dengue Shock When Patients Develop DSS: • 3 to 6 days after onset of symptoms Initial Warning Signals: • Disappearance of fever • Drop in platelets • Increase in hematocrit Alarm Signals: • Severe abdominal pain • Prolonged vomiting • Abrupt change from fever to hypothermia • Change in level of consciousness (irritability or somnolence) Four Criteria for DHF: • Fever • Hemorrhagic manifestations • Excessive capillary permeability • 100,000/mm3 platelets
  • 30. CENTERS FOR DISEASE CONTROL AND PREVENTION Four Grades of DHF  Grade 1 • Fever and nonspecific constitutional symptoms • Positive tourniquet test is only hemorrhagic manifestation  Grade 2 • Grade 1 manifestations + spontaneous bleeding  Grade 3 • Signs of circulatory failure (rapid/weak pulse, narrow pulse pressure, hypotension, cold/clammy skin)  Grade 4 • Profound shock (undetectable pulse and BP)
  • 31. CENTERS FOR DISEASE CONTROL AND PREVENTION Problem in Dengue Fever/Dengue Hemorrhagic Fever in Indonesia  High viral transmission  Economical impact : Cost of treatment Lost of productivity  Mortality especially in children about 2 %  Not effective prevention: vector eradication no effective vaccine
  • 32. CENTERS FOR DISEASE CONTROL AND PREVENTION years 1996 1994 1992 1990 1988 1986 1984 1982 1980 1978 1976 1974 1972 1970 1968 70000 60000 50000 40000 30000 20000 10000 0 Incidence of Dengue Hemorrhagic Fever in Indonesia 1968-1996 Ministry of Health, Rep of Indonesia
  • 33. CENTERS FOR DISEASE CONTROL AND PREVENTION years 1996 1994 1992 1990 1988 1986 1984 1982 1980 1978 1976 1974 1972 1970 1968 50 40 30 20 10 0 Mortality of Dengue Hemorrhagic Fever in Indonesia 1968-1997 Ministry of Health, Rep of Indonesia
  • 34. Treatment of Dengue Haemorrhagic Fever  Fluids  Rest  Antipyretics (avoid aspirin and non-steroidal anti-inflammatory drugs)  Monitor blood pressure, hematocrit, platelet count, level of consciousness
  • 35. Tatalaksana DBD pada Dewasa Protokol 1 Penanganan Tersangka ( Probable ) DD/DBD dewasa tanpa syok Protokol 2 Pemberian cairan pada tersangka DBD dewasa di ruang rawat Protokol 3 Penatalaksanaan DBD dengan peningkatan Ht > 20 % Protokol 4 Penatalaksanaan Perdarahan Spontan pada DBD dewasa Protokol 5 Tatalaksana sindroma syok Dengue pada dewasa
  • 36. Keluhan DBD (Kriteria WHO 1997) Hb, Ht Normal Tromb > 100.000/mm³ Observasi Rawat jalan Periksa Hb, Ht dan leuko, tromb/ 24 jam Hb, Ht normal Trombo < 100.000 Hb, Ht meningkat Trombo N / turun Protokol 1. Penanganan Tersangka ( Probable ) DD / DBD Dewasa tanpa syok Rawat Inap ( Protokol 2 )
  • 37. Protokol 2. Pemberian cairan pada tersangka DBD dewasa di ruang rawat Suspek DBD Perdarahan Spontan dan Masif (-) Syok (-) Hb,Ht (n) Tromb. <100.000 Hb,Ht 10-20% Tromb. <100.000 Hb,Ht > 20% Tromb.<100.00 0 ◘Infus Kristaloid ◘Hb,Ht,Tromb. tiap 24 jam Infus Kristaloid Hb,Ht,Tromb. tiap 12 jam Protokol 3
  • 38. Volume cairan kristaloid per hari yang diperlukan : 1500 + 20 X ( BB dalam kg – 20 ) Contoh : BB 50 kg : 1500 + 20 X ( 50 – 20) = 1500 + (20 x 30) = 1500 + 600 = 2100 ml (Pan American Health Organization: Dengue and Dengue Hemorrhagic Fever: Guidelines for Prevention and Control. PAHO: Washington,D.C,1994:67). Awasi kadar elektrolit darah jika memungkinkan.
  • 39. Protokol 3. Penatalaksanaan DBD dengan peningkatan Ht > 20 % 5 % defisit cairan Kristaloid 6 – 7 ml/kg/jam PERBAIKAN TIDAK MEMBAIK Kristaloid 5 ml/kg/jam Kristaloid 10 ml/kg/jam TIDAK MEMBAIK Kristaloid 15 ml/kg/jam MEMBURUK  SYOK PROTOKOL 4 / 5 PERBAIKAN Kristaloid 3 ml/kg/jam PERBAIKAN STOP CAIRAN PERBAIKAN PERBAIKAN 3-4 jam 2 jam 3 jam 24-48 jam
  • 40. Protokol 4. Penatalaksanaan Perdarahan Spontan pada DBD dewasa KASUS DBD : Perdarahan Spontan dan Masif : - Epistaksis tidak terkendali - Hematemesis melena - Perdarahan otakSyok (-) Hb, Ht, Trombo, Leuko, Pemeriksaan Hemostasis (KID) Golongan darah, uji cocok serasi Transfusi komponen darah : * PRC (Hb<10 g %) * FFP (APTT > 1,5 X normal ) * TC (Tromb.<100.000) * Pemantauan Hb, Ht, Tromb. Tiap 4-6 jam * Ulang pemeriksaan hemostasis 24 jam kemudian KID +: HEPARINISASI 5000 – 10.000 / 24J
  • 41. Protokol 5. Tatalaksana Syok pasien Dewasa AIRWAY BRAETHING : O2 1 – 4 l/menit CIRCULATION : 10 – 20 ml/kgBB 20 – 30 MENITPERBAIKAN TETAP SYOK Kristaloid 20-30 ml/kgBB 20-30 menit TETAP SYOK Ht k Koloid 10-20 ml/kg/BB tetes cepat 10-15 menit Transfusi PRC 10 ml/kgBB Ht k TETAP SYOK Koloid hingga maksimal 30 ml/kgBB TETAP SYOK Pasang CVP Hipovolemik Normovolemik KRISTALOID TETAP SYOK Inotropik , Vasoaktif Koreksi : As/Bs, Electr,Glikemia, Anemia, KID, Infeksi Sekunder PERBURUKAN
  • 42. AIRWAY BREATHING : O2 1 – 4 l/menit CIRCULATION : 10 – 20 ml/kgBB Protokol 5. Tatalaksana Syok pasien Dewasa 20 – 30 MNT PERBAIKAN Kristaloid 7 ml/kg/jam dalam 1 jam PERBAIKAN Kristaloid 5 ml/kg/jam dalam 1 jam PERBAIKAN Kristaloid 3 ml/kg/jam dalam 1 jam STABIL 24 – 48 JAM PERBURUKAN TETAP SYOK
  • 43. Protokol pemberian zat inotropik / zat vasoaktif Dopamin 5 mg/kg/mnt dititrasikan sampai 10 mg/kg/mnt Sasaran : MAP > 60 mmHg. Gagal Dobutamin 5 mg/kg/mnt + Norepinefrin 0,05 – 0,1 mg/kg/mnt 10 mg/kg/mnt 1 mg/kg/mnt Epinefrin 0,1 mg/kg/mnt Dititrasikan setiap 0,1 mg/kg/mnt Max 2 mg/kg/mnt GAGAL ?
  • 44. Indikasi masuk ICU :  Syok yang tidak dapat teratasi maksimal 2 jam  Syok berulang  Syok dengan perdarahan hebat  Syok dengan penyulit seperti : kegagalan pernafasan, ensefalopati, gagal jantung, dll.
  • 46. Kriteria Pemulangan pasien DBD 1. Tidak demam selama 24 jam tanpa antipiretik 2. Nafsu makan membaik 3. Klinis tampak perbaikan 4. Hematokrit stabil 5. Tiga hari setelah renjatan teratasi 6. Jumlah trombosit > 50.000 7. Tidak dijumpai distres pernafasan
  • 47. KESIMPULAN  Indonesia merupakan negara tropis dengan risiko kemungkinan terjadinya DBD cukup tinggi  Menegakkan diagnosis serta penatalaksanaan Dengue tidaklah mudah  Penanganan pasien DBD melalui pedoman tatalaksana yang ada, di sarana pelayanan kesehatan  Pedoman ini perlu disosialisasikan ke semua petugas kesehatan, pemantauan, evaluasi implementasinya agar penanganan DBD dapat maksimal