Académique Documents
Professionnel Documents
Culture Documents
Albumin
3.5-5.5 g/dl
Bilirubin
0.3-1.1 mg/dl
Unconjugated Bilirubin 0.2-0.7
mg/dl
Conjugated Bilirubin 0.1-0.4
mg/dl
AST (SGOT)
10-40 U/ml
ALT (SGPT)
5-35 U/ml
Alkaline Phospatase 10-30 U/ml
Protrombin Time 12-14 sec
Serum
Bilirubin
Serum
Albumin
PT
Ascites
Encephal
opathy
A
< 2.0
B
2.0-3.0
C
> 3.0
> 3.5
2.8-3.5
< 2.8
1-4
sec
-
4-6 sec
> 6 sec
slight
Minim
al
Moderat
e
Advance
d
Bilirubin (Stoelting)
degradation product of hemoglobin
and mioglobin
unconjugated bilirubin (formed
peripher)
liver (conjugated)
+1
+2
Mudah
lelah
Senang
panas
Senang
dingin
Keringat
berlebih
Gugup
+2
Nafsu
makan
naik
Nafsu
makan
turun
BB naik
BB turun
+3
-5
+5
+3
+2
-3
-3
+1
Tanda
Ada
Pembesaran
tiroid
Bruit pada
tiroid
Exoftalmus
+3
Tidak
Ada
-3
+2
-2
Retraksi
palpebra
Palpebra
terlambat
Hiperkinesis
+2
Telapak
tangan lembab
Nadi <
80x/menit
+1
Nadi >
90x/menit
+3
Fibrilasi atrial
+4
Neurophurology
Cerebral Metabolic Rate
Cerebral Blood Flow
Cerebral Perfusion Pressure
a. Autoregulasi
MAP = 50-150 mmHg
b. PaCO2
ET CO2 25-30 mmHg =
PaCO2 29-34 mmHg
c. PaO2
+2
+4
+2
-2
-3
Urology
Ren
simpatis
Spinal cord
Parasimpatis
-2
Ureter
Bladder
Parasimpatis
Prostat Urethra
T8-L1
T10-L1
vagus
S2-S4
T11-L2
S2-S4
T11-L2
S2-S4
Creatinin Clearance
CCT
= (140-umur) x BB
72 x CR
Normal : 100-120
Decreased renal reserve
Mild renal impairment
60-100
40-60
25-40
< 25
< 10
TURP
soluti
on
osm
olal
ity
0
advant
age
Disadvantage
visibil
ity
hemolysis,
hemoglobinemi
a, hyponatremia
Glyci
ne (1,
5%)
200
Transient post
op visual
Sorbit
ol (2,
7%)
Mann
itol
(0,
57%)
165
TURP
syndr
ome
=
glycin
e
Isoos
molar
soluti
on
Destil
ed
water
275
..
115
- Somnolen
110
- Nausea
kejang
coma
Perdarahan
TURP syndrome
Bladder perforation
Hipotermia
Septikemia
DIC
Hyponatremia
Hipoosmolalitas
Fluid overload CHF, Pulmonary
oedem, Hypotension
Hemolysis
Toksisitas
cairan
hyperglycinemia, hyperammonemia,
hyperglycemia,
intravascular
volume expansion
Massive
diuresis
Pencegahan TURP Syndrome
ECG
Komplikasi TURP
Widening
QRS .
- QRS
melebar
- ST elevasi
VT / VF
HEPATO-RENAL SYNDROME
Hepatorenal syndrome is a functional
renal defect in patients with cirrhosis
that usually follows gastrointestinal
bleeding, aggressive dieresis, sepsis or
major surgery. It is characterized by
progressive oligouria with avid sodium
retention, azotemia, intractable ascites
and very high mortality rate.
Diagnostic
criteria
(Longnecker)
for
HRS
Major criteria
- Acute/chronic liver disease with
advanced hepatic failure and portal
hypertension
- Depressed GFR with a serum
creatinin > 1,5 mg/dl or CCT < 40
ml/mm
- Absence on shock, ongoing
bacterial infection, fluid loss and
treatment
with
nephrotic
medications
- No sustained improvement in renal
function after withdrawal of
diuretics and fluid resuscitation with
1.5 l isotonic saline
- Proteinuria < 500 mg/dl and no
evidence of obstructive nephropathy
Minor criteria
- Oligouria
- Urine sodium < 10 mEq/l
- Urine
osmolality
>
plasma
osmolality
- Urine RBC < 50 ..
- Serum sodium concentration < 130
mEq/l
SVR
Reduce effective volume renal
hypoperfusion
Cystic Fibrosis
Bronchiectasis
Bronchiolisis
Kriteria Hemodialisa
Bupivacai
n
Dos
e
5
- Anuria
7.5
10
disorders
involving
the
pleura, chest wall
diaphragm
Ex.
Pulmonary
oedem, ARF
Restrictive P.D
Acute and chronic
intrinsic
pulmonary
Bloc
k
T5
(T4T7)
T8
(T4T11)
T8
(T6T10)
T5
(T4T7)
Duratio
n
123
Discharg
e
181
144
202
194
260
343
471
Fentanyl: 10-25 mg
Clanidine: 15-45 mg
Epinefrin: 0,1-0,6 mg
Neostigmin: 6,25-50 mcg
Upper abdomen
T4
T6
Vaginal delivery
T10
L2
Perineal
S2-S5
Thyroid Storm
-
Hyperperexia
Takikardia
Altered consciousness
delirium)
Hypotension
Pancronium
Indirect acting adrenergic agonist
(agitation,
Normal= 0,3-3,0.
- Kanalis Inguinalis
Kraniolateral:
annulus
inguinalis
Medial bawah: tuberkulum
pubikum,
dibatasi
annulus
inguinalis
Atap: atap m. obliquus interna
Dasar: lig. Inguinale
Vesiculer ..
RBK di bronchioli
RB
THALASSEMIA (Barosh)
-
Autosomal
resesif
anemia,
insufficient production of one of the
globin , , , . Paling sering
thalassemia.
Temuan klinik: anemia, hemolisis,
hyperplasia sumsum tulang
Anemia mikrositer hipokrom
thalassemia
Thalassemia Major
Homozygous thalassemia
Severe + thalassemia
Heterozygous thalassemia
Severe + thalassemia
Thalassemia Intermedia
Homozygous hemoglobin
Thalassemia
minor
mild
reductions in and globin
production
Protokol transfusi:
Paliatif
transfusion,
hyper
transfusion,
super
transfusion
paliatif, daerah yang .
Hypertransfusion menjaga Hb 910 mg/dl
Supertransfusion Hb > 12 g/dl
- Management of anesthesia
Tergantung berat / tidaknya anemia
.. eritropoiesis can produce
.. and narrowing of m. nasal
.
Epidural contraindication relative
pada presence of .. bone
marrow in .
Epidural
Absolute:
Patient refusal
Uncorrected hipovolemia
Increased ICP
Infection of site
Allergic to amide/eter LA
Relative: Coagulopathy
Platelet count < 100.000
Uncooperative patient
Severe
Sepsis
Hypertension
Controversial: Inadequate training
.
.
.
Diabetes Mellitus
Diagnosis elevated fasting plasma
glucose (> 140 mg/dl) and blood
glucose (> 126 mg/dl)
Komplikasi akut: DKA
Hipoglikemia
Komplikasi kronis: Hipertensi
CAD (Coronary Artery
Disease)
Myocardial infarction
Congestive
Heart
Failure
Diastolic dysfunction
Peripheral and cerebral
vascular disease
Peripheral
and
autonomic
Renal failure
Seizure disorders (EPILEPSY)
- Caused: .
- abnormalities: hyperglycemia,
hyponatremia, hyperthermia, drug
totality
- Klasifikasi berdasarkan: kehilangan
kesadaran dan fokus kejang
- Treatment: anti-epileptikum
Partial Seizures: carbamazepine,
phenytoin, valproat (barbiturates,
.seizures)
Antiepilepsi
propofol + thiopental
BGA
Menurut Cottrel
Epilepsi: 1. Partial: simple partial
Complex partial
Convulsive
2. Generalized
Phenitoin:
hipotensi,
cardiac
arithmia,
gingival
hyperplasia,
anemia aplastic
Valproat: hepatic failure
Carbamazepine can cause dysplasia,
leukopenia, hyponatremia
Status epileptikus: keadaan kejang 2x
atau lebih, dimana antara 2 kejang itu
tidak ada fase sadar
Treatment: A, B, C
Hipoglikemia D50 60 cc
anesthetics: