Table 2.
List of factors potentially affecting HCV treatment decisions*
1 |
Possible future health problems you expect from not treating Hepatitis C |
2 |
Expected effectiveness of treatment (in terms of the treatment’s typical impact or lack of impact on virus levels) |
3 |
Expected overall side effects of treatment |
4 |
Expected depression side effects in particular |
5 |
Expected flu-like side effects in particular |
6 |
Expected fatigue side effects in particular |
7 |
Amount of time needed to finish the entire treatment |
8 |
The need to inject one of the treatment medications with a needle |
9 |
Having to remember to take several medications according to a schedule from the doctor |
10 |
Possible Hepatitis C treatment alternatives not discussed by your doctor |
11 |
Need for a liver biopsya |
12 |
How Hepatitis C, the disease, has affected (or not affected) other people’s lives |
13 |
How Hepatitis C treatment has affected other people’s lives |
14 |
The stage of your Hepatitis C (for example, your liver status) |
15 |
Whether or not you had Hepatitis C symptoms |
16 |
Other health issues in addition to Hepatitis C, [for women] including pregnancy or possible pregnancy |
17 |
Any substance abuse issues (alcohol or recreational street drugs) |
18 |
The need for more information about Hepatitis C treatments |
19 |
The extent of your will power when you decide to do something (such as starting a treatment)a/ The extent of your will power when you decide to do something (such as finishing a treatment)b |
20 |
The effect of the condition of Hepatitis C on your ability to reach life goals |
21 |
The effect of the condition of Hepatitis C on the lives of others, such as your family members |
22 |
The effect treatment might have on your ability to meet work responsibilitiesa/ The effect of the treatment on your ability to meet your work responsibilitiesb |
23 |
The effect treatment might have on your ability to meet family responsibilitiesa/ The effect of the treatment on your ability to meet your family responsibilitiesb |
24 |
Your ability to pay for treatment |
25 |
The effect treatment might have on your ability to earn moneya/ The effect of treatment on your ability to earn moneyb |
26 |
The stability of your housing situation |
27 |
The emotional support you could expect from friends, family, support groups, and/or religion if you were to start treatmenta/ Emotional support from your friends, family, support groups, and/or religionb |
28 |
Your doctor’s advice |
29 |
Your relationship with doctors and nurses in terms of the encouragement and knowledge they typically provide |
30 |
Organizational help from doctors and nurses in things like managing appointments and helping with medications |
31 |
How easy or hard it is to see doctors or nurses (for example traveling to the doctor’s office and making appointments) |
32 |
Potential for being treated differently or judged if you were to start treatmenta/ Being treated differently or judged because of the treatmentb |
33 | Your ability to get information during treatment about your virus levels and how likely the treatment will work for youa/ Information during treatment about your virus levels and how likely the treatment will work for youb |
*Study participants were asked to provide an importance rating for each factor. Naïve patients provided ratings in regards to HCV treatment initiation; unless otherwise noted, all other patients provided ratings based on the factors’ importance to treatment initiation and completion.
aPatients rated the factor only in regards to importance to HCV treatment initiation.
bPatients rated the factor only in regards to importance to HCV treatment completion.