Table 1.

AYAs’ and caregivers’ demographics and responses to selected items on the FKAQ

AYAs, n = 20Caregivers, n= 15
n (%)n (%)
Demographics 
Genotype 
 Hemoglobin SS/SB0 14 (70) — 
 Hemoglobin SC/SB+ 6 (30) — 
Median Age (IQR) 16.5 (5) — 
Relationship status 
 Single 19 (95) 5 (33) 
 Serious relationship/marriage 1 (5) 10 (67) 
Race* 
 Black/African American 17 (85) 11 (73) 
 African 4 (20) 2 (13) 
 White 1 (5) 1 (7) 
 Asian 2 (10)  
Other  1 (7) 
Education 
 Less than an associate's/ bachelor’s degree — 10 (67) 
 Associate's/bachelor’s or higher degree — 5 (33) 
Household income 
 ≤$35,000 — 7 (47) 
 >$35,000 — 7 (47) 
 Not reported — 1 (7) 
FKAQ knowledge items 
 1. I received information about my (my son’s) fertility (the ability to have a biological child) from my sickle cell provider. 9 of 18 (50) 9 of 15 (60) 
 2. I received information about my (my son’s) fertility (the ability to have a biological child) from my parents (my family). 7 of 18 (39) 3 of 15 (20) 
 3. I received information about my (my son’s) fertility (the ability to have a biological child) from the media or Internet. 3 of 18 (17) 2 of 14 (14) 
 4. My (my son’s) sickle cell disease might make it difficult for me (him) to have a biological child in the future. 4 of 19 (21) 4 of 15 (27) 
 5. The treatment I (my son) receive/received for my (my son's) sickle cell disease might make it difficult for me (him) to have a biological child in the future. 2 of 19 (11) 1 of 15 (7) 
 6. I would like more information about how sickle cell disease and its treatment could affect my (my son’s) ability to have a biological child. 13 of 18 (72) 9 of 15 (60) 
 7. I have enough knowledge about my (my son’s) fertility (ability to have a biological child). 4 of 19 (21) 7 of 15 (47) 
Testing interest/barriers 
 8. Do you know what semen analysis (or sperm analysis) is? 6 of 20 (30) 3 of 15 (20) 
 9. Do you know how a semen (or sperm) sample is collected? 7 of 20 (35) 7 of 15 (47) 
AYAs, n = 20Caregivers, n= 15
n (%)n (%)
Demographics 
Genotype 
 Hemoglobin SS/SB0 14 (70) — 
 Hemoglobin SC/SB+ 6 (30) — 
Median Age (IQR) 16.5 (5) — 
Relationship status 
 Single 19 (95) 5 (33) 
 Serious relationship/marriage 1 (5) 10 (67) 
Race* 
 Black/African American 17 (85) 11 (73) 
 African 4 (20) 2 (13) 
 White 1 (5) 1 (7) 
 Asian 2 (10)  
Other  1 (7) 
Education 
 Less than an associate's/ bachelor’s degree — 10 (67) 
 Associate's/bachelor’s or higher degree — 5 (33) 
Household income 
 ≤$35,000 — 7 (47) 
 >$35,000 — 7 (47) 
 Not reported — 1 (7) 
FKAQ knowledge items 
 1. I received information about my (my son’s) fertility (the ability to have a biological child) from my sickle cell provider. 9 of 18 (50) 9 of 15 (60) 
 2. I received information about my (my son’s) fertility (the ability to have a biological child) from my parents (my family). 7 of 18 (39) 3 of 15 (20) 
 3. I received information about my (my son’s) fertility (the ability to have a biological child) from the media or Internet. 3 of 18 (17) 2 of 14 (14) 
 4. My (my son’s) sickle cell disease might make it difficult for me (him) to have a biological child in the future. 4 of 19 (21) 4 of 15 (27) 
 5. The treatment I (my son) receive/received for my (my son's) sickle cell disease might make it difficult for me (him) to have a biological child in the future. 2 of 19 (11) 1 of 15 (7) 
 6. I would like more information about how sickle cell disease and its treatment could affect my (my son’s) ability to have a biological child. 13 of 18 (72) 9 of 15 (60) 
 7. I have enough knowledge about my (my son’s) fertility (ability to have a biological child). 4 of 19 (21) 7 of 15 (47) 
Testing interest/barriers 
 8. Do you know what semen analysis (or sperm analysis) is? 6 of 20 (30) 3 of 15 (20) 
 9. Do you know how a semen (or sperm) sample is collected? 7 of 20 (35) 7 of 15 (47) 
*

Participants had the option to select all that apply for this category.

Data are the proportion (%) of AYAs and caregivers who responded “yes.”

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