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Table 8 New model development

From: Performance of critical care prognostic scoring systems in low and middle-income countries: a systematic review

Study

Ahluwalia et al. (1999) [29]

Riviello et al. (2016) [43]

Riviello et al. (2016) [43]

Nimgaonkar et al. (2004) [35]

Nimgaonkar et al. (2004) [35]

Model

New score

Rwanda MPM (R-MPM)

Simplified R-MPM

Artificial Neural Network (ANN 22)

Artificial Neural Network (ANN 15)

Source

Prospective cohort

Prospective cohort

Prospective cohort

Prospective cohort

Prospective cohort

Participants

Consecutive admissions (>13 years) to eight-bed medical ICU, India; inclusion period NR;

participant age range 13–80, mean = 46

Consecutive patients (>15 years) admitted to two ICUs in different hospitals; exclusion criteria: not specified; August 2013–October 2014;

participant age range 34 years (IQR 25–47) (median)

Consecutive patients (>15 years) admitted to two ICUs in different hospitals; exclusion criteria: not specified; August 2013–October 2014;

participant age range 34 years (IQR 25–47) (median)

All consecutive patients (>12 years) admitted to 17-bed medical–neurological ICU, tertiary referral hospital, India; January 1996–May 1998

All consecutive patients (>12 years) admitted to 17-bed medical–neurological ICU, tertiary referral hospital, India; January 1996–May 1998

Outcomes

Hospital mortality

Hospital mortality

Hospital mortality

Hospital mortality

Hospital mortality

Predictors

1. pH (at admission); 2. serum albumin (at admission); 3. heart rate (at 48 hours); 4. GCS (at 48 hours); 5. bilirubin (at 48 hours)

Only the following five variables were included: 1. age; 2.confirmed or suspected infection within 24 hours of ICU admission; 3. hypotension or shock as a reason for ICU admission; 4. heart rate at ICU admission; 5. GSC at time of admission

Altered mental status on ICU admission (present vs not present) used in place of the GCS score in the R-MPM (see previous model)

22 APACHE II variables

15 APACHE II variables with the highest information gain (measured by calculation of entropy)

Sample size

79

427

427

2962

2962

Missing data

Not reported

Normal values attributed as in original study;

two patients excluded due to lack of discharge status

Normal values attributed as in original study;

two patients excluded due to lack of discharge status

Not reported

Not reported

Model development

Based on APACHE II (Knaus et al. 1985 [10]) and 11 other clinical and laboratory parameters. Backward step method used to remove non-significant (p > 0.05) variables (of univariate analysis)

Based on the 16 MPM III (initial) and additional variables. Variables for inclusion in model selected from the univariate analyses, based on their predictive power (as determined by p < 0.05) as well as their ease of capture based on experience, the proportion of missing values in the dataset, and their clinical significance

Based on the 16 MPM III (initial) and additional variables. Variables for inclusion in model selected from the univariate analyses, based on their predictive power (as determined by p < 0.05) as well as their ease of capture based on experience, the proportion of missing values in the dataset, and their clinical significance

Artificial Neural Network trained on an Indian patient dataset using the 22 APACHE II variables

Artificial Neural Network trained on an Indian patient dataset using the 15 APACHE II variables with the highest information gain (measured by calculation of entropy)

Model performance

Discrimination measured in terms of AUROC, sensitivity and specificity. Multivariate and univariate regression

Discrimination measured in terms of AUROC.

Calibration measured as Hosmer–Lemeshow.

Multivariate and univariate regression

Discrimination measured in terms of AUROC.

Calibration measured as Hosmer–Lemeshow.

Multivariate and univariate regression

Discrimination measured as AUROC.

Calibration measured as Hosmer–Lemeshow

Discrimination measured as AUROC.

Calibration measured as Hosmer–Lemeshow

Model evaluation

Developmental dataset only, no further evaluation (compared with APACHE II at 48 hours)

Internal validation with bootstrapping (compared with MPM III (initial))

Internal validation with bootstrapping (compared with MPM III (initial))

Data from 1962 patients were used to train the neural network using a back-propagation algorithm. Data from the remaining 1000 patients were used for testing this model and comparing it with APACHE II

Data from 1962 patients were used to train the neural network using a back-propagation algorithm. Data from the remaining 1000 patients were used for testing this model and comparing it with APACHE II

Results

New score ROC: 0.90, sensitivity: 98.2%, specificity: 66.6%.

APACHE II (after 48 hours) ROC: 0.74, sensitivity: 92.8%, specificity: 23.6%

Rwanda MPM (R-MPM) AUROC: 0.81 (0.77–0.86),

HL: χ2 = 11.94 (p = 0.154).

MPM III (initial)

AUROC: 0.72,

HL: χ2 = 17.66 (p = 0.024)

Simplified R-MPM

AUROC: 0.76,

HL: χ2 = 11.46 (p = 0.177).

MPM III (initial)

AUROC: 0.72,

HL: χ2 = 17.66 (p = 0.024)

ANN 22 AUROC: 0.87, HL

H statistic:

χ2 = 22.4 (p < 0.05).

APACHE II

AUROC: 0.77,

HL

H statistic:

χ2 = 123.5 (p < 0.05)

ANN 15

AUROC: 0.88,

HL

H statistic:

χ2 = 27.7 (p < 0.05).

APACHE II

AUROC: 0.77,

HL

H statistic:

χ2 = 123.5 (p < 0.05)

  1. APACHE Acute Physiology and Chronic Health Evaluation, MPM Mortality Probability Models, ICU intensive care unit, GCS Glasgow Coma Score, IQR interquartile range, HL Hosmer–Lemeshow statistic, AUROC area under the receiver operating characteristic