Research Article

Rapid Dantrolene Administration with Body Temperature Monitoring Is Associated with Decreased Mortality in Japanese Malignant Hyperthermia Events

Table 4

Clinical and biochemical presentations at dantrolene administration.

Survivor ()Deceased () value
Median(IQR)Median(IQR)

Maximum rate of increase in body temperature (°C/15 min)0.80(0.50-1.00)930.65(0.53-1.32)80.81
Maximum body temperature (°C)39.7(38.8-40.9)10441.8(39.9-43.0)100.0017
Maximum PaCO2 (mmHg)70.8(56.4-89.0)8294.8(48.7-152.1)70.25
Maximum ETCO2 (mmHg)75.0(65.0-96.5)8184.0(71.3-113.3)40.45
Lowest arterial pH7.17(7.05-7.23)826.96(6.82-7.11)80.0014
Lowest arterial base excess-4.35(−8.80-−2.00)78-14.05(−19.9-−11.4)8< 0.0001
Highest creatinine kinase (IU/L)3304(1259-25766)9128064(1723-223740)80.12
Highest serum myoglobin (ng/mL)1181(659-1340)3524900(1340-112000)60.007
Highest potassium (mEq/L)5.3(4.5-6.0)716.2(5.0-7.6)90.021
Dose of dantrolene (mg/kg)1(0.75-1.94)270.98(0.90-1.45)70.70
Temperature at dantrolene administration (°C)39.1(38.5-40.3)4341.6(39.9-42.8)10< 0.001
Anesthetic induction to first MH sign (min)60.0(30-130)8790.0(15-165)100.85
Interval from first MH sign to dantrolene administration (min)45.0(25.0-75.0)43100.0(75.0-135.0)50.007

Subjects with missing data were excluded. IQR: interquartile range; PaCO2: arterial partial pressure of carbon dioxide; ETCO2: end-tidal carbon dioxide; MH: malignant hyperthermia.