Table 1.
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CHARACTERISTICS OF KEY INFORMANTS | (N = 38) | % |
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Gender | ||
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Female | 33 | 87 |
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Male | 5 | 13 |
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Age (years) | ||
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25–34 | 5 | 13 |
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35–44 | 15 | 39 |
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45–54 | 13 | 34 |
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55–64 | 5 | 13 |
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Years of experience in complex care | ||
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Less than 6 months | 3 | 8 |
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6 to 11 months | 2 | 5 |
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1 to 2 years | 4 | 11 |
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3 to 4 years | 8 | 21 |
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5 to 10 years | 15 | 39 |
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11 to 20 years | 6 | 16 |
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Role in CCKO strategy | ||
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Leadership Table member* | 11 | 29 |
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Nurse practitioner | 8 | 21 |
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Physician | 6 | 16 |
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Allied health professional | 4 | 11 |
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Home and community care coordinator | 5 | 13 |
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Administrative staff | 4 | 11 |
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CHARACTERISTICS OF PARENT CAREGIVERS AND THEIR CHILDREN WITH MEDICAL COMPLEXITY | (N = 10) | % |
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Of the Parents Gender | ||
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Female | 9 | 90 |
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Male | 1 | 10 |
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Home setting | ||
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Urban | 5 | 50 |
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Rural | 5 | 50 |
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Education level | ||
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Some post-secondary | 2 | 20 |
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Completed secondary/high school | 1 | 10 |
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Completed post-secondary | 7 | 70 |
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Family structure | ||
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Never married- single parent | 3 | 30 |
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Married- dual parent | 6 | 60 |
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Divorced- single parent | 1 | 10 |
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Of the Parent’s Child with Medical Complexity | ||
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Age in months, median (IQR) | 28.5 (99.75) | |
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Gender | ||
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Male | 5 | 50 |
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Female | 5 | 50 |
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Primary diagnoses | ||
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Neurologic | 4 | 40 |
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Congenital/Genetic defect | 3 | 30 |
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Malignancy | 2 | 20 |
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Miscellaneous/Not elsewhere classified | 1 | 10 |
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# of diagnoses, mean (SD) | 5.9 (2.0) | |
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Medications used, mean (SD) | 4.7 (2.5) | |
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Technology devices used, mean (SD) | 2.4 (1.5) | |
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Hospital outpatient visits, mean (SD) | 14 (17.0) | |
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Characteristics of key informants, parent caregivers and their children with medical complexity, n (%) unless otherwise stated.
* Key Informants include clinical and administrative leads of regional hub sites, and ex officio members.