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Research ArticleOriginal Research

A Qualitative Study of Depression in Primary Care: Missed Opportunities for Diagnosis and Education

Barry G. Saver, Victoria Van-Nguyen, Gina Keppel and Mark P. Doescher
The Journal of the American Board of Family Medicine January 2007, 20 (1) 28-35; DOI: https://doi.org/10.3122/jabfm.2007.01.060026
Barry G. Saver
MD, MPH
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Victoria Van-Nguyen
BA
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Gina Keppel
BA
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Mark P. Doescher
MD, MSPH
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  • Article
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Article Figures & Data

Tables

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    Table 1.

    Participant Statements about Prediagnosis Understanding of Depression

    • I don’t think I had much of an understanding. I knew for myself though how it felt—it wasn’t good.

    • I didn’t really have a concept of it. I had heard of people who had trouble getting out of bed but I didn’t grasp—know what it meant.

    • Initially, I was embarrassed. I thought it was laziness, ignorance, something I could change. That lasted for a pretty long time.

    • Suicide. That’s it. Basically, I have seen people depressed, and I didn’t understand it until it happened to me. I thought it was so bad that I would end up killing myself.

    • My understanding of depression was that one got depressed because of a culmination of events in their life that they normally just blew off or denied ever happened. The shadow of those events would move in.

    • View popup
    Table 2.

    Participant Statements about Missed Diagnoses of Depression

    Patient unwilling or unable to raise the question of depression:
    • I never knew how to express it, and I had a shame in expressing it. I felt the shame in mentioning it to my family, even though my family had a whole depression issue. So if I couldn’t talk to my family, then how could I have talked about it to a doctor?

    • I was good at hiding it, until I just fell apart one day.

    Provider unsuspecting, disinterested, or dismissive:
    • I had no indication that they were thinking about that while they were trying out other things. I presented myself with physical symptoms, and that was it.

    • I think that because the subject was about my pain, other matters at hand, that they didn’t ask about my sleeping habits, my mood, appetite. My doctor couldn’t have known.

    • I guess maybe I wasn’t really sure what was going on. And so, I probably didn’t mention it as problems I was having, and I perceived (my primary care doctor) as someone more interested in physical issues.

    • I had one person tell me it was all in my head, that there was nothing anyone could help.

    • When I mentioned it to my primary care doctor, he said, “Well, you smile—you don’t seem to be depressed.” So I just stopped mentioning it; that was about 2 years ago.

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    Table 3.

    Participant Statements Regarding Sources of Information about Depression

    Information from primary care providers:
    • None. Not in the past either.

    • Quite frankly, [PCP told me] nothing. I just told them what I felt, and they identified it as depression. They didn’t go into the details, and I didn’t ask for the information.

    • I actually don’t remember too much. She said that it is nothing to get upset about, and that it is common and she will get help for it.

    • She [PCP] referred me to one of the patient libraries. So I went there and got some info on depression and taking medications and how that should help and what to do if it doesn’t.

    • I had one person tell me it was all in my head, there was nothing anyone could help. That’s why I went to [mental health clinic]. I knew they had counseling and medication.

    Information from mental health providers:
    • I was given some brochures, but they seem like they’re written for sixth graders.

    • I was seeing a psychiatrist; they explained about my depression and why I got it.

    • I was given some literature to read and I had discussions with my counselor about it … No more information except research on my own.

    • They [mental health services agency] gave me some flyers that I read. They asked me which category fit me best.

    • The second doctor was very good at gauging my personality, figuring out the best way to talk to me.

    • I got a lot of information from the psychiatrist I saw.

    Other sources of information:
    • I remember going to bookstores and reading.

    • My ears would pick up on things if I heard a show on TV, radio, a new article in a magazine

    • I went on the Internet, Web MD, looking for what the symptoms were, what I should be looking for, if it was triggered from a traumatic experience.

    • Just recently heard about synapses, serotonin, what they do. I guess maybe on the Internet I learned it was hereditary, so I can blame my mom and dad… . I think the more I learn about it, the more I understand it and can deal with it instead of just shutting down and assuming I’ll always be depressed. I like learning the scientific reasons for it.

    • I’ve seen that ad on TV—the little bouncing head, talking about things not getting from one synapse to another; I do understand there’s an organic element there. That’s nice to know, otherwise I could just blame myself. I learned more from watching that commercial on television [than from my provider].

    • As far as information about medicine and whatnot, I’d heard of Prozac, Paxil; I really do my research by asking people I know… . Media is a very powerful tool. All those commercials I used to make fun of, I understand now—the [drug name] commercials, …

    • View popup
    Table 4.

    Participant Statements about Barriers to Getting Information about Depression

    Lack of motivation to learn when depressed:
    • It [getting information from provider] would have been very helpful. I could have looked by myself or gone to the library. But when you are depressed, you just want things handed to you.

    • They didn’t go into the details, and I didn’t ask for the information. I don’t want to blame them for not telling me more, because I didn’t invite or encourage them to share.

    • I was seeing a psychiatrist, they explained about my depression and why I got it. I wasn’t focusing on that much. I was thinking about a better way to kill myself.

    Stigma, denial:
    • I was afraid of counseling because I felt that my family would disown me. I ended up taking medication and I was afraid of dealing with people about this.

    • I guess shame, embarrassment. The Internet is better—I can just do it on my own.

    • Not wanting to just accept that that was going on. You have to get a job, move on, maintain some kind of normality.

    • She said, “When you’re ready, I’ve got a whole bunch of stuff you might want to read, you might find yourself in some of it.” She’d start slowly with the uncomfortable stuff. I just wasn’t ready to hear it.

    Limited provider responsiveness:
    • I would have liked to know how medication or counseling, both would work for me. But the doc was like she was doctor and she would know better… . They are not able to show full concern because they are low in staff and funding. The frustration shows because you have to make it clear that you need more than this. For a patient who did not know how to make it clear, you are in a Catch-22.

    • The first counselor referred me to some pamphlets, kind of brushed over the whole subject. He seemed like he had reached a level of detachment with his job. Just totally unmemorable.

    • I did try to talk to doctors about depression. It just wasn’t working. I let my doctors know that. That doctor kept trying to tell me this was the best thing for me; I know there are other medications.

    Information-seeking style:
    • I would never sit down and read something about medicine. It has never interested me. I learned more from watching that commercial on television.

    • I don’t seek out information, but if I come across it, then I will take it and read it.

    • View popup
    Table 5.

    Participant Statements about Participation in Treatment Decisions

    No perceived choice:
    • They just handed me a drug and said go on it right now··· I felt rushed along, given a prescription, told this will fix it.

    • We never discussed any treatment plans. They just diagnosed and then gave me Zoloft and that’s it.

    Lack of sufficient information to make a choice:
    • I just got the option that we got medication or counseling available. I don’t know what’s required of you and it was scary. I didn’t know how to ask any of these questions.

    • Just about medication. I don’t really feel like there were options except for the different types of medications, which might have different side effects. And I might decide which side effects I potentially have to deal with. It did seem that there were not any psychological components brought up.

    Trust practitioner to make the choice:
    • I trust my doctor implicitly, so I didn’t question. I felt perhaps that she was making the best choice based on her knowledge of me, which was pretty vast… . I would probably like to see what other treatment options are. I fear getting confused by the onslaught of treatment options.

    • I’ve always been like going to a car mechanic–′Treat me. Just do what you need to do.′

    Made an informed choice:
    • Yes, when we had the initial interview, he [PCP] left that open and up to me, whether to have some concurrent counseling along with medication or just try the medication. He left that up to me and facilitated that role or would refer me to someone else, whatever I wanted.

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The Journal of the American Board of Family Medicine: 20 (1)
The Journal of the American Board of Family Medicine
Vol. 20, Issue 1
January-February 2007
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A Qualitative Study of Depression in Primary Care: Missed Opportunities for Diagnosis and Education
Barry G. Saver, Victoria Van-Nguyen, Gina Keppel, Mark P. Doescher
The Journal of the American Board of Family Medicine Jan 2007, 20 (1) 28-35; DOI: 10.3122/jabfm.2007.01.060026

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A Qualitative Study of Depression in Primary Care: Missed Opportunities for Diagnosis and Education
Barry G. Saver, Victoria Van-Nguyen, Gina Keppel, Mark P. Doescher
The Journal of the American Board of Family Medicine Jan 2007, 20 (1) 28-35; DOI: 10.3122/jabfm.2007.01.060026
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