Skip to main content

Table 3 Important features of EHRs with embedded CDSSs on which consensus was achieved in this study

From: Merits, features, and desiderata to be considered when developing electronic health records with embedded clinical decision support systems in Palestinian hospitals: a consensus study

  

Round 02

Round 03

Importance weight (%)

Source of the item

#

Items

M

IQR

%A

M

IQR

%A

M

SD

Demographic characteristics of the patient

 1

The body weight of the patient

8

2

88

NA

11.2

3.8

B

 2

The measure units of weight (gm, kg, pounds)

8

2

92

NA

10.6

2.9

L

 3

The working weight of the patient that was used for dose calculations (for example, 5 kg instead of 5.1 kg)

7

2

84

NA

9.3

3.0

L

 4

Date on which the weight of the patient was measured

7

2

79

NA

8.6

3.2

B

 5

The height of the patient

6

5

53

8

2

75

8.1

2.8

B

 6

The measure units for height (cm, m, in)

5

4

51

7

2

76

7.6

2.4

L

 7

The date on which the height of the patient was measured

4

4

48

7

2

75

7.2

2.5

B

 8

The body surface area of the pediatric patient

7

2

79

NA

6.8

2.3

L

 9

The measure units of the body surface area

7

2

82

NA

6.0

2.1

L

 10

The date on which the body surface area was measured

7

1

85

NA

5.4

3.1

L

 11

The body mass index of the patient

7

2

76

NA

4.8

3.2

L

 12

The date on which the body mass index of the patient was measured

7

2

75

NA

3.9

2.9

L

 13

Time on which the weight of the patient was measured

7

4

71

7

2

82

2.9

2.6

L

 14

The time on which the height of the patient was measured

4

5

46

7

2

76

2.7

2.4

L

 15

The time on which the body surface area was measured

7

2

84

NA

2.6

2.0

L

 16

The time on which the body mass index of the patient was measured

6

4

61

7

2

75

2.3

1.7

L

Prescribing medications

 1

Prompting a mode of selection for specifying the dose (for example mg, μg, mL, … etc.) of the medication prescribed

9

1

100

NA

11.8

2.6

B

 2

Prompting a mode of selection for specifying the frequency (number of times) the medication needs to be administered (for example, once daily, twice daily, three times daily, ...etc.)

9

1

100

NA

9.4

3.2

B

 3

Prompting a mode of selection for specifying the route by which the medication would be administered (for example, oral, intravenous, intramuscular, … etc.)

8

1

99

NA

8.8

3.6

B

 4

Prompting a mode of selection for specifying the dosage form “formulation” (for example, tablet, capsule, syrup, ...etc.) of the medication prescribed

8

2

91

NA

8.2

2.9

B

 5

Prompting a mode of selection for specifying the number of dosing units to be administered each time (for example, one tablet, two tablets, … etc.)

9

1

93

NA

7.5

2.6

L

 6

Allowing search and/or providing a mode of selection (for example a drop-down menu) for all medications available on the hospital’s formulary including their non-proprietary names and brand (branded-generic) names

7

2

79

NA

6.9

2.4

L

 7

Prompting a mode of selection for specifying the date on which the medication was prescribed

9

1

95

NA

6.4

2.1

L

 8

Prompting a mode of selection for specifying the duration for which the medication administration should be continued

8

1

97

NA

6.2

2.8

L

 9

Prompting a mode of selection for specifying the date on which the medication administration should be started

7

2

93

NA

5.8

2.7

L

 10

Prompting a mode of selection for specifying the times at which the medication doses should be administered (for example, at 8:00 am, 2:00 pm, … etc.)

8

1

92

NA

5.3

2.4

L

 11

Prompting a mode of selection for specifying the date on which the medication administration should be discontinued

9

1

92

NA

5.1

1.9

B

 12

Prompting a mode of selection for specifying the time on which the medication administration should be discontinued

9

1

94

NA

4.8

1.8

L

 13

Prompting a mode of selection for specifying the medication administration in relation to meals

8

1

92

NA

4.3

1.6

B

 14

Prompting a mode of selection for specifying the maximal number of doses to be administered in 24 h for medication prescribed as “when needed” (PRN)

8

1

89

NA

3.8

1.2

B

 15

Prompting a mode of selection for specifying the name of the physician who prescribed the medication

9

1

96

NA

3.2

1.1

L

 16

Ability to suggest other suitable substitutes (other medications from the same pharmacological class)

6

4

54

7

2

76

2.5

1.4

I

Checking prescriptions and alerts

 1

Ability to assess suitability of the dose in view of the patient’s conditions like renal and/or hepatic functions

8

1

92

NA

13.6

3.6

B

 2

Clear instructions to guide prescribers on the procedures to follow when a medication order to be discontinued or changed

9

2

92

NA

12.8

3.1

B

 3

Ability to check for and provide warnings on potential drug-drug interactions

8

2

92

NA

11.3

3.5

L

 4

Ability to check for and provide warnings on potentially contraindicated medications for the patient

7

2

89

NA

10.2

3.2

B

 5

Ability to check for and provide warnings on potential drug-food interactions

5

3

61

7

2

75

9.6

3.3

L

 6

Ability to check for and provide warnings on potential drug-herb interactions

6

3

68

7

1

78

8.5

2.9

L

 7

Ability to provide warnings regarding any potential medication adverse reactions in view of the patient’s conditions

6

3

59

7

2

76

7.3

2.6

B

 8

Ability to recommend evidence-based dose suitable for the patient

7

3

69

7

1

79

6.4

2.8

B

 9

Ability to check for and provide warning when another medication from the same pharmacological class (duplication) is prescribed

7

4

69

7

2

76

5.2

2.9

L

 10

Ability to provide prompts on special precautions or procedures to administer the prescribed medication (if any)

7

3

74

7

2

77

3.8

2.3

L

 11

Ability to alert the prescriber if the dosage form(s) prescribed was (were) of slow or modified release

6

3

69

7

2

76

2.6

1.8

L

 12

Ability to enter reason(s) (justification) why another medication from the same pharmacological class (duplication) is prescribed

7

2

79

NA

2.4

1.6

L

 13

Ability to add reasons (justification) for not changing the medication or dose in the event of an adverse medication reaction

5

3

46

7

2

75

2.1

1.9

L

 14

Ability to enter reason(s) (justification) why the dose was different from the evidence-based recommended one

7

2

78

NA

1.7

1.2

L

 15

Ability to enter reason(s) (justification) why the dosing frequency was different from the evidence-based recommended one

6

4

58

7

2

75

1.4

1.3

L

 16

Ability to enter reason(s) (justification) why the duration of medication administration was different from the evidence-based recommended one

5

4

56

7

2

76

1.1

0.9

L

Patient’s identity

 1

The first name of the patient

9

1

100

NA

12.2

3.7

B

 2

The father’s name of the patient

9

1

100

NA

11.3

3.2

B

 3

The grandfather’s name of the patient

9

1

100

NA

10.7

4.1

B

 4

The family name (surname) of the patient

9

1

100

NA

9.2

3.6

B

 5

The unique national identification number of the patient

6

4

62

7

2

76

8.7

2.9

B

 6

The gender of the patient

9

1

100

NA

8.1

3.1

B

 7

The date of birth of the patient

9

1

100

NA

7.5

2.9

B

 8

The age of the patient

7

2

89

NA

7.1

3.1

L

 9

The measure units of age (years, months, or days)

8

2

91

NA

6.8

2.8

L

 10

The gestational age of the pediatric patient (for neonates)

7

4

71

7

2

77

6.1

1.9

L

 11

The corrected gestational age of the pediatric patient (if the neonate was a preterm)

6

4

68

7

2

76

5.3

2.8

L

 12

The date on which the age of the patient was calculated

7

2

88

NA

3.5

2.6

L

 13

The telephone number of the patient/their parent(s)/guardian(s) in case of a pediatric patient

7

3

74

7

2

79

2.1

1.2

B

 14

The home address of the patient

7

3

72

7

2

78

1.4

1.1

B

Patient assessment

 1

Prompts to enter the presenting symptoms of the patient

8

1

99

NA

12.6

3.2

B

 2

Prompts to enter the vital signs of the patient

9

1

99

NA

11.3

3.5

B

 3

Ability to enter and/or automatically import results of laboratory tests ordered for the patient

9

1

99

NA

10.2

2.8

L

 4

Ability to enter and/or automatically import results of medical images ordered for the patient

9

1

99

NA

9.3

2.6

L

 5

Ability to enter other co-morbidities the patient might be suffering from

8

1

97

NA

8.9

2.3

B

 6

Ability to enter all relevant information on prescription medications the patient is/was taking

8

1

96

NA

8.2

2.9

B

 7

Ability to enter all relevant information on other non-prescription medications the patient is/was taking

8

2

94

NA

7.3

3.1

I

 8

Ability to enter all relevant information on allergies to medications the patient suffered from

9

1

100

NA

7.0

2.2

B

 9

Ability to enter all relevant information on adverse medication reactions the patient suffered from

9

1

100

NA

6.3

1.9

L

 10

Ability to update patient’s data and integrating new laboratory, imaging, and vital sign measurements

9

1

98

NA

6.0

1.8

L

 11

Ability to transfer patient’s data into the patient’s electronic medical record

8

1

96

NA

4.8

2.0

L

 12

Ability to enter information on congenital defects of the patient

8

1

94

NA

4.6

1.8

I

 13

Ability to enter all relevant information on herbal medicines used by the patient

7

3

74

7

2

81

3.5

1.6

L

Quality of alerts

 1

Suggestions and alerts should be evidence-based, provide a reference or references, and level of evidence

6

4

52

7

2

75

16.9

3.2

L

 2

Suggesting evidence-based and up-to-date recommendations, guidelines, and/or protocols to prescribe medications

6

3

74

7

2

79

14.2

2.6

B

 3

Alerts regarding allergy should distinguish between a serious potential allergy and minor side effect of the medication

7

2

76

NA

12.9

3.8

L

 4

Alerts and suggestions should provide clear information on relative risk of harm for the given patient

6

4

51

7

2

76

11.3

3.5

L

 5

Ability to give warning when the prescribed dose differed from the recommended dose

6

4

61

7

2

76

8.6

2.9

B

 6

Ability to recommend evidence-based dosing frequency suitable for the patient

7

4

62

7

2

76

7.3

3.1

B

 7

Ability to recommend evidence-based duration of medication administration

7

3

60

7

1

75

6.8

2.8

L

 8

Clear instructions to guide prescribers on writing the reason for discontinuing or changing a medication order

8

2

87

NA

5.3

3.1

L

 9

Prompts to indicate if additional charts other than the medication chart was used for the patient (for example other charts for intravenous fluids, nutrition, … etc.)

8

1

89

NA

4.8

2.1

B

 10

Clear instructions to obtain parent/guardian authorization to allow for immunization as per the national program, in case, immunization was due for a pediatric patient

7

4

71

7

1

82

4.3

1.8

L

 11

The system should not allow the use of non-standard abbreviations/nomenclature

8

2

94

NA

4.1

1.6

B

 12

Compulsory review of medications prescribed before saving and validating orders

7

3

73

7

1

85

3.5

1.8

L

Admission and discharge of the patient

 1

The hospital’s admission number assigned to the patient at the time of admission

7

2

90

NA

20.2

2.3

B

 2

The date on which the patient was admitted to the hospital

8

2

97

NA

15.8

2.1

B

 3

Name(s) of the ward(s) to which the patient was (were) admitted

9

2

94

NA

13.1

3.2

B

 4

The name of the physician under whose care the patient was admitted to the hospital

8

2

94

NA

11.9

4.1

L

 5

The date on which the patient was discharged from the hospital

8

2

93

NA

11.1

2.6

B

 6

The name of the physician who decided to discharge the patient

9

1

95

NA

9.1

3.1

B

 7

Bed(s) number(s) that was (were) assigned to the patient during their admission to the hospital

9

1

98

NA

8.0

2.9

B

 8

Name of the hospital to which the patient was admitted

9

2

93

NA

4.9

2.5

I

 9

Name of the physician who entered the patient information and verified that all details were correct

7

2

88

NA

2.9

2.1

L

 10

The time on which the patient was discharged from the hospital

7

2

91

NA

1.9

1.7

B

 11

The time on which the patient was admitted to the hospital

7

2

93

NA

1.1

1.2

B

General features

 1

The system should be as user friendly as practically possible providing easy to use interfaces

9

1

96

NA

21.1

4.2

I

 2

Alerts should be clear and specify exactly why they were displayed

8

2

91

NA

17.3

3.6

B

 3

The system should provide a prepackaged entry forms allowing accurate and comprehensive patient assessment

8

2

94

NA

15.6

4.3

L

 4

The system should allow retrieval and viewing of all and/or selected patient’s specific information as the user desires

7

2

88

NA

13.1

3.9

B

 5

Users should provide reasons when opting to over-ride system recommendations

7

2

88

NA

10.2

2.8

L

 6

Provided entries should be customizable in case the user needed to modify some of them

7

2

88

NA

8.6

2.7

B

 7

Ability to remind the user to complete tasks and activities that were not completed or selected for follow up

7

2

77

NA

5.6

2.1

B

 8

Users should be able to decline suggested recommendations

6

4

63

7

2

78

4.9

1.9

I

 9

Alerts and suggestions should pop-up when really necessary to avoid prescriber alert desensitization

6

3

48

7

1

77

3.6

1.7

B

Diseases and making diagnosis

 1

Ability to enter diagnosis

8

1

98

NA

39.7

10.3

B

 2

Ability to access to offline, online, and searchable databases and references related to diseases and differential diagnosis

8

2

91

NA

32.1

6.2

B

 3

Ability to provide hints for potential diagnosis based on the data entered into the assessment section

7

2

87

NA

28.2

4.6

L

  1. %A percentage of panelists who voted 7–9 on the item, B both (literature and interviews), CDSSs clinical decisions support systems, EHRs electronic health records, I interviews, IQR interquartile range, L literature, M median, NA not applicable, SD standard deviation