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Erratum to 5-Years Later – Have Faculty Integrated Medical Genetics into Nurse Practitioner Curriculum?

  • Ann H. Maradiegue EMAIL logo , Quannetta T. Edwards and Diane Seibert
Published/Copyright: January 11, 2014

Erratum in: International Journal of Nursing Education Scholarship 2013;10(1):DOI 10.1515/ijnes-2012-0007. After online publication of ijnes-2012-0007 we realized that some of the data for Tables 2, 3 and 4 were in error. Please find the revised Tables 2, 3, and 4 with correct data.

Table 2

Advance practice (APRN) faculty’s self-reported level of comfort teaching genetic/genomic concepts and conditions – years 2010 and 2005 (N = 85 and N = 40, respectively)

Genetic/genomic condition & conceptsYear 2010Year 2005**Percent difference in 2010 & 2005*
YesNoYesNo
N (%)N (%)N (%)N (%)Yes to comfort in teaching genetics/genomics (%)
Basic genetic concepts
Autosomal dominant59 (69.4)26 (30.6)23 (58.0)17 (42.0)11.4
Autosomal recessive60 (70.6)25 (29.4)23 (58.0)17 (42.0)12.6
X-linked56 (65.9)29 (34.1)22 (55.0)18 (46.0)10.9
Mitochondrial inheritance42 (49.4)43 (50.6)10 (25.0)30 (75.0)24.4
Three-generation pedigree67 (78.8)18 (21.2)16 (40.0)24 (60.0)38.8
Genetic/genomic conditions
Tay-Sachs disease50 (58.8)35 (41.2)15 (37.0)25 (63.0)21.8
Cystic fibrosis59 (69.4)26 (30.6)18 (45.0)22 (55.0)24.4
Breast/ovarian cancer84 (99.0)1 (1.0)23 (58.0)17 (42.0)41.0
Colon cancer71 (83.6)14 (16.4)22 (55.0)18 (45.0)38.6
Hemochromatosis71 (83.6)14 (16.4)16 (35.4)24 (64.6)48.2
Sickle cell anemia75 (88.2)10 (11.8)24 (60.0)16 (40.0)28.2
Thalessemia70 (82.4)15 (17.6)22 (55.0)18 (45.0)27.4
Fragile-X syndrome46 (54.2)39 (45.8)20 (50.0)20 (50.0)4.2
Huntington’s disease55 (64.7)30 (35.3)14 (35.0)26 (65.0)29.7
Phenylketonuria49 (57.6)36 (42.4)19 (48.0)21 (52.0)9.6
Gaucher’s disease28 (33.0)57 (67.0)6 (15.0)34 (85.0)18.0
Myotonic dystrophy31 (36.6)54 (63.4)11 (28.0)29 (72.0)8.6
Klinefleter’s syndrome46 (54.1)39 (45.9)14 (35.0)26 (65.0)19.1
Diabetes and genetics46 (54.1)39 (45.9)22 (55.0)18 (45.0)−0.9
Cardiovascular conditions and genetics49 (57.6)36 (42.4)21 (53.0)19 (48.0)4.6
Trisomy 13, 18 or 2148 (56.4)37 (43.6)17 (43.0)23 (58.0)23.4
Familial hypercholesterolemia55 (60.7)30 (39.3)19 (48.0)21 (52.0)12.7
Other
Polymerase chain reaction20 (23.5)65 (76.5)6 (15.0)34 (85.0)8.5
Gene therapy33 (38.8)52 (61.2)11 (28.0)29 (73.0)10.8
Online Inheritance in Man (OMIM)30 (35.3)55 (64.7)N/AN/A
Table 3

Advance practice (APRN) faculty’s self-reported level of integration of genetic concepts and conditions into advance practice curricula – years 2010 and 2005 (N = 85/N = 40, respectively)

Genetic/genomic topicsLevel of integration**Percent changefor high-level integration (%)
Year – 2010Year – 2005*
NoneMinimalHighNoneMinimalHigh
N (%)N (%)N (%)N (%)N (%)N (%)
Basic genetic concepts
Autosomal dominant5 (6.4)57 (66.5)23(27.1)6 (15.0)25 (62.0)9 (23.0)4.1
Autosomal recessive6 (7.1)56 (65.8)23 (27.1)6 (15.0)25 (62.0)9 (23.0)4.1
X-linked8 (9.4)60 (70.7)17 (19.9)7 (17.0)25 (63.0)8 (20.0)−0.1
Mitochondrial inheritance12 (14.1)61 (71.8)12 (14.1)17 (42.0)20(50.0)3 (8.0)6.1
Three-generation pedigree5 (6.9)43(54.8)37(38.3)8 (20.0)22 (55.0)10 (25.0)13.3**
Genetic/genomic conditions
Tay-Sachs disease5 (6.4)63 (73.6)17 (20.0)12 (30.0)23 (57.0)5 (13.0)7.0
Cystic fibrosis2 (2.0)58 (65.0)25 (33.0)6 (15.0)21 (54.7)13 (30.3)2.7
Breast/ovarian cancer1 (1.2)48 (54.8)36 (44.0)3 (7.0)21 (53.0)16 (40.0)4.0
Colon cancer2 (2.4)48 (56.4)35 (41.2)6 (15.0)20 (50.0)14 (35.0)6.2
Hemochromatosis11 (12.9)28 (32.9)46 (54.2)17 (42.0)20 (50.0)3 (8.0)46.2**
Sickle cell anemia2 (2.0)46 (49.8)37 (48.2)5 (13.0)23 (57.0)12 (30.0)18.2**
Thalessemia3 (3.5)61 (71.8)21 (24.7)9 (23.0)22 (54.5)9 (22.5)2.2
Fragile-X syndrome11 (12.9)59 (69.9)15 (17.2)14 (35.0)20 (50.0)6 (15.0)2.2
Huntington’s disease6 (7.1)65 (76.5)14 (16.4)14 (35.0)23 (57.0)3 (8.0)8.4
Phenylketonuria5 (6.0)44 (55.2)36 (38.8)14 (35.0)15 (37.0)11 (28.0)10.8
Gaucher’s disease27 (31.8)52 (61.1)6 (7.1)30 (75.0)1 (2.0)9 (23.0)–15.9
Myotonic dystrophy25 (29.4)52 (61.1)8 (9.5)24 (60.0)14 (35.0)2 (5.0)4.5
Klinefleter’s syndrome10 (11.8)57 (67.0)18 (21.2)16 (40.0)19 (47.0)5 (13.0)8.2
Diabetes and genetics11 (12.9)58 (61.9)16 (25.2)3 (8.0)22 (54.0)15 (38.0)–12.8
Cardiovascular conditions and genetics7 (8.2)29 (34.1)49 (57.7)5 (13.0)21 (52.0)14 (35.0)22.7**
Trisomy 13, 18 or 2110 (11.8)57 (64.6)18 (23.6)13 (33.0)19 (47.0)8 (20.0)3.6
Familial hypercholesterolemia7 (8.2)48 (56.5)30 (35.3)13 (33.0)14 (34.0)13 (33.0)2.3
Other
Polymerase chain reaction28 (32.9)45 (52.9)12 (14.2)29 (72.0)7 (18.0)4 (10.0)4.2
Gene therapy13 (15.3)65 (74.4)7 (10.3)20 (50.0)16 (40.0)4 (10.0)0.3
Table 4

Advance practice (APRN) faculty who self-reported formal education or training in genetics/genomics in years 2010 and 2005 (N=85 and N=40, respectively)

Genetic/genomic concepts & conditionsYear 2010*Year 2005% Difference
YesNoYesNo“Yes” faculty training/educationYear 2010 and 2005
N (%)N (%)N (%)N (%)
Basic genetic concepts
Autosomal dominant6 (7.1)79 (92.9)15 (37.5)25 (62.5)–30.4%
Autosomal recessive3 (3.5)82 (96.5)15 (37.5)25 (62.5)–34.0%
X-linked3 (3.5)82 (96.5)15 (37.0)25 (63.0)–33.5%
Mitochondrial inheritance7 (8.2)78 (91.8)8 (20.0)32 (80.0)–11.8%
Three-generation pedigree7 (8.2)78 (91.8)13 (32.5)27 (67.5)–24.3%
Genetic/Genomic conditions
Tay-Sachs disease4 (4.7)81 (95.3)9 (22.5)31 (77.5)–17.8
Cystic fibrosis4 (4.7)81 (95.3)10 (25.0)30 (75.0)–20.3
Breast/ovarian cancer4 (4.7)81 (95.3)**7 (18.5)**31 (81.5)–13.8
Colon cancer4 (4.7)81 (95.3)9 (22.5)31 (77.5)–17.8
Hemochromatosis5 (5.9)80 (94.1)6 (15.0)34 (85.0)–9.1
Sickle cell anemia4 (4.7)81 (95.3)9 (22.5)31 (77.5)–17.8
Thalessemia3 (3.5)82 (96.5)11 (27.5)29 (72.5)–24.0
Fragile-X syndrome4 (4.7)81 (95.3)10 (25.0)30 (75.0)–20.3
Huntington’s disease4 (4.7)81 (95.3)8 (20.0)32 (80.0)–15.3
Phenylketonuria4 (4.7)81 (95.3)8 (20.0)32 (80.0)–15.3
Gaucher’s disease3 (3.5)82 (96.5)4 (10.0)36 (90.0)–6.5
Myotonic dystrophy3 (3.5)82 (96.5)7 (17.5)33 (82.5)–14.0
Klinefleter’s syndrome4 (4.7)81 (95.3)9 (22.5)31 (77.5)–17.8
Diabetes and genetics4 (4.7)81 (95.3)9 (22.5)31 (77.5)–17.8
Cardiovascular conditions and genetics4 (4.7)82 (96.5)9 (22.5)31 (77.5)–17.8
Trisomy 13, 18 or 212 (2.4)83 (97.6)11 (27.5)29 (72.5)–25.1
Familial hypercholesterolemia3 (3.5)82 (96.5)8 (20.0)32 (80.0)–16.5
Other
Polymerase chain reaction4 (4.7)81 (95.8)5 (12.5)35 (87.5)–7.8
Gene therapy4 (4.7)81 (95.8)7 (17.5)33 (82.5)–12.8

Published Online: 2014-01-11

©2013 by Walter de Gruyter Berlin / Boston

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  31. 5-Years Later – Have Faculty Integrated Medical Genetics into Nurse Practitioner Curriculum?
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