Dr. Streett noticed an abnormality in the stomach during the procedure and ordered an ultrasound of the liver.
Following is my letter of complaint to member services:
3/01/2010
To: Kaiser Member Services
Re: Colonoscopy Mistreatment of 2/24/10
From: Hunter R. Austin
Below follows a letter that was dropped off at Member services Kaiser Vallejo. I’m sending it again, to you, because I received a letter from you on the 9th of March about said grievance. Your stated that if I had anything to add you would need it by the 12th of March. Short notice? Sure seems like it. I’ve had to put a number of projects on hold to sit down and get this done. Again, a Kaiser inconvenience. So, to me, this is important enough to drop everything because my life feels like it’s at an impasse and I am clearly exhibiting mental, spiritual and physical changes since the day in question.
Also, your letter states that I have “concern regarding your (my) dissatisfaction with the quality of care and service you (I) have received from Dr. Paul Rubin of the Kaiser Permanente Vallejo Medical Center Medicine Department.” While this is also true, it is a SEPARATE issue as stated in the Re: Colonoscopy Mistreatment of 2/24/10, at the very beginning of my letter. I want to keep it that way until the matter at hand is resolved. At which time I may file a separate grievance. So here’s the original (with a few minor changes that I’ve since remembered) and also, below the original, what I’ve added since...
To whom it may concern,
I had an experience at Kaiser Vallejo GI dept. yesterday(when I started to write this) 2/24/10 that was so painful, degrading, and horrifically unprofessional that, if I could afford it, I would change my health insurance today. As well as look into what my legal options are for this level of improper care. Also, judging by what Dr. Streett wrote in the “after visit summary” which was “The preparation was not ideal, with retained stool.” If that was the case then this procedure should have been postponed until the conditions WERE ideal. After all, since day one with Dr. Rubin (over a month ago, during which I’ve had extra pain on top of my chronic pain) one of my original complaining symptoms has remained, time and time again, including the morning of and before my procedure, “ It feels like there’s still stool stuck in there, or something blocking the stool from coming out.” Why would one of your doctors, after having read my chart before the procedure (unless they actually didn’t) continue with a test that, in order to get the optimum result, the entirety of the intestinal tract, colon, etc… needs to be as clean and clear as is possible? Also nowhere in the “after visit summary” does it mention my screaming, begging, and pleading to stop!
I got there at 8am, in pain, and I left, a few hours later, in worse pain. Then again (this has been recurring, on and off, for the last 3 weeks) the pain in my stomach woke me up at approx. 3:50am the next morning, and was so intense (9-10) I took a Percocet, and then another one twenty-five minutes later, and as I write this, the pain wavers between a 4 and 5…close to where it’s been for the last two-three weeks with little or no relief and my test appt.’s being spread out over that time instead of getting me in there and finding out what the heck is wrong! You can read my records and (hopefully it’s well documented) find out what’s been going on as I’m quite frustrated with the fact of how many times I’ve had to tell it and how many of the EXACT same questions have been asked by different Dr.,’s…sometimes even the same ones asking the same questions! I don’t expect perfection, but a modicum of professionalism would be nice.
But the long and short of it is, four months ago I had a bad belly ache with nausea and constipation, that lasted overnight, during which there were a few (non-related?) bloody noses, then went away. Same exact scenario happened around two and a half months ago. A bit under a month ago, same thing, at which time I made an appt. with Dr. Rubin. During this time, pain and constipation, loss/fear of appetite, feeling bloated after just a few bites, extreme fatigue, and attacks of #9-10 pain occurring regularly and lasting from 45 min. to 3 hours during which time I tried to move my bowels for relief but was unsuccessful. Dr. Rubin said it was blockage and gas and prescribed Rx’s to no avail. I ended up in the emergency room that following weekend. Monday I spoke with Rubin (after two unanswered emails) and told him I wanted to see a GI, and he said, “Oh, I completely agree with you.” Gee thanks doc. At this juncture I wondered whether My Dr. had been taking me seriously all this time, or was it the all too common and usual ego-laden, off the cuff diagnosis…next patient please, kind of thing.
So I saw Dr. Cohen, he was leaving for vacation, so he set me up with Dr. Streett. My Last Colonoscopy, about five years ago at the VA; I went in (after the fasting and go-lightly treatment) they sedated me and when I awoke I was fine, no discomfort during or after the procedure. When I asked the GI nurse at Kaiser about the sedation she said that most of the patients fall asleep, so I wasn’t that concerned. Although I had asked, clearly, to be completely sedated, instead I was given Benadryl. An allergy medicine that makes one drowsy. That is not sedation.
My Colonoscopy at Kaiser felt like a real pretty-boys first night in jail with the Aryan brotherhood. I was held down on the bed while they rammed, twisted, pumped, and anything else painful that one can do with a fat tube in your anus was done. Let’s just hope I’m not the one in a hundred that’s had something punctured. Throughout the entire procedure I was told about twenty times “It’s almost over, it’s almost over, and it’s almost over…and stop moving, don’t tighten up, stay this way, don’t move your leg, and on and on.” I was screaming and yelling Stop!, Stop!, the whole time, to which their reply was always. “It’s almost over.” People in the pre-op, and waiting room (one of which was my mom to drive me home) heard everything. My mom was totally freaked out and started crying when we got to the car.
I understand now why the VA sedated me. Smart move. But during these last few days, at home and in pain, I spoke with friends and family, most of which have had these procedures, more than once, and they were flabbergasted with my story. All of their experiences, while not referred to as pleasurable, not one person had any pain during or after, and those who were sedated, upon arising, felt like nothing happened. Two of my friends were awake, and while they watched the procedure on the monitors said they experienced “little if any” discomfort.
I am still in constant pain at about a 2 to 4 level, even driving over bumps in the road is like a punch in the left side of my gut. I’ve had two attacks, one the morning after the procedure and another 45 minute or so attack yesterday, very early morning, and they always start with it feels like I have to move my bowels, but sometimes I do and other times I can’t, but even when I do have a bowel movement, it does not abate the pain. My energy level is so low that if I try to read I just end up falling asleep. It took me three days to finish this letter because I can’t seem to focus on anything except the traumatic experience Kaiser put me through. Even talking, or writing about it totally stresses me out, which as far as having had a heart attack a little over a year ago is certainly not good for me. Isn’t the first thing Doctors promise to do in the Hippocratic oath is “no harm,” what happened to that?
What to do now? I want a diagnosis before the end of the week. At this point I don’t care about protocol, scheduling, vacations, or anything else except my diagnosis. I have been in (more than usual) pain for a month, with about eight to ten horrendously painful lower left/center abdomen attacks. I cannot and will not put up with this any longer. I will make myself available today, and then again from Wednesday the 3rd forward, for any tests that could result in a diagnosis.
Hunter R. Austin
OK, since then I‘ve been keeping notes on a regular basis-
I realized, after a couple, maybe less, days, what I had been so scared about. Before a colon/sigmoid-oscopy I was informed that there was a very low percentage chance of “something” (I don’t remember exactly what could be punctured, but the chance of death I do remember) being punctured that could result in death! This has been stressing me out ever since. Have you completely forgotten that I have a cardiac history as well, and that my heart attack and subsequent scares have been triggered by stress? Lately, I’ve woken up in the middle of night scared, like I know I had a bad dream, but I can’t remember what it was, and after a little while of being up I start to think about that ordeal y’all put me through, and I can feel my blood pressure going up. It’s like some kind of bad thing is happening to me and I have to take a Zanax to go back to sleep. I feel like you guys (Kaiser) only see one problem, and totally forget about the rest of the person. Like a horse with blinders.
I had my scheduled ultrasound on the 5th and the tech performing the procedure said that it was imperative I get another CT scan immediately, and sent me to radiology to make an appt. What ensued there was first “take a number and have a seat” but after a few minutes I got up and went back to where they did the ultrasound and said that I thought this needed to be done right away and all I’m doing is waiting out there, at which point the receptionist came back and in hushed tones (I heard my last name mentioned a couple of times but not much else.) I can only imagine what was being said, which in and of itself puts a patient ill at ease. Then the receptionist asked me to follow her, and we went back out front, and (from what I could glean and from the questions I asked) there was over an hour of checking with Dr.’s back and forth, because my primary and my GI were both on vacation.
I was then scheduled for a CT scan that day at 5pm, it was now 2:30. I asked the woman running the front desk/appts. AOC (whose attitude, by the way, couldn’t have been more laissez-faire) if that was enough time for the contrast drink to have an effect. She said “I’m sure the doctors know what they’re doing.” Maybe in her experiences they did but not in mine. She also said that she was faxing or emailing (I didn’t quite hear which) my Rx right over to the new pharmacy right now and to hurry and go get it and start to drink it over the next two hours. I went right there, a five minute walk, and they had no idea what I was talking about. Again, mayhem ensued, telephone calls, record checking, repeatedly telling me there was no record of it, etc...after asking for the pharmacist a number of times and being told to “Just hold on a minute” and “Gimme a sec, I’m looking for it.” I ratcheted up my requests on an audible scale until I got the pharmacist involved. Finally at 3:05 the Pharmacist began to explain how this medication should be taken, which involved an overnight process. I told her (why didn’t she know this? Was a note in my records forgotten?) that my test was in two hours, at which point she gave me the Rx and said “Oh OK, is that going to be enough time?” I thought back to the receptionist saying “I’m sure the doctors know what they’re doing.”
After the CT scan I asked the tech how it looked, was it clear, and readable? He assured me it looked great and that because of the urgency that someone would be contacting me immediately. Friday, Saturday, and Sunday went by without a word from Kaiser. On Monday Kaiser called to tell me my Rx (an unrelated, online ordered Rx for pain) was ready and to come by and pick it up.
The woman I spoke on the phone with said that she was from Dr. Rubin’s office, and that he was on vacation but the covering Dr. had approved my refill. I asked her if there was any word about the urgent CT scan I had done on Friday. No idea, we don’t handle that, and basically a go bleep yourself attitude, and I know nothing. She didn’t say “Let me see if I can find out” but instead she told me that I needed to call that dept. or the advice nurse...not even an offer to connect me with the right person who might be able to help me. I know how I’ve been dealt with, and I make it a point to watch how your other patients are dealt with, I say dealt with for a reason, which is; a good 75% of the time there’s no “care” involved. So when I got my hard copy of the Rx I asked the front desk woman ( who has always been helpful as well as nice) at Dr. Rubin’s office if she could help and she said “let me check it out.” A half a minute later she asked me to have a seat and the covering (Rubin still on vacation) Dr. would like to speak with me. 20 minutes later a nurse, not a doctor, came out and said the CT was unreadable and I had to go down to GI dept. and get another scheduled! I had to go down there! There’s no way this nurse or the Dr. that “supposedly” deemed the CT scan, which the tech said looked great—unreadable, could call and get me another appt.? I walked away laughing, which was a darned sight better than what I felt like doing, at that point. It feels like I’m in a war with Kaiser, a war to see who will outlast who, a war of wills. A war where it’s me against the bureaucratic behemoth that is Kaiser.
I’d say a strong 25 to 30% (that I’ve come in contact with) of your staff, top to bottom, seem to be doing well in the criteria with which I use to judge. Unfortunately only 5% of them are doctors. And the two that I’ve had the most interaction with were sadly not part of that meager 5%. In fact Dr. Streett, although probably not a direct cause of any cardiac issues to come, I know has already had some kind of psychological effects with which I have no experience. It would be a presumptuous comparison to rape with a foreign object, but still in all, that’s where my brain takes me when I think about that morning. The way I was held down, how I begged for it to stop, and the pain, my god, that kind of non-medicated pain! In a hospital no less. I couldn’t look anyone in the eye afterward...not even my mom. I felt so embarrassed, childlike, and emotionally out of control. It was like I was holding on to the edge of a cliff with my fingertips and I just couldn’t do it!
I also seem to be very short-tempered lately, and up-tight in general at home and at work. My wife has had to put up with these unwarranted outbursts, and has been very understanding and supportive, but I still feel like it’s only my problem and I have to deal with it alone. It’s too embarrassing to talk about what happened and how I feel. But I’m trying to put that aside for now because my anger outweighs everything else. And when I think about this possibly happening to someone else, someone not as strong as me, and the discussions my wife and I have about this situation, I KNOW I have to go through with it.
At work it’s like I’m self-sabotaging my business. I can’t help it; I’m not happy-and it shows, usually I’m quite gregarious, and smiling, quick to make a joke and laugh, connect with people; all the things a good salesperson does. But now I just feel limp and wrung out, I watch the clock, and I find fault with everyone and everything. I don’t like my job anymore because there’s too many people near me. They just keep coming and coming with no end in sight.
3/7/10 This morning I feel nauseous and, at the same time, have to move my bowels. I don’t know which to do first. The pain level in my lower left abdomen is at a 4, and climbs to six when I start/try (very little still coming out and it still feels like something is stuck in there...same original symptoms I came to you with) to move my bowels, not ‘attack’ level, but enough to defocus my world from everything but the symptoms. Also not bad enough to take a Percocet (on top of the methadone) because then I’m looking at 4 or 5 hours of giddy incapacitation. It’s been over a month now with the most minimal amount of relief and maximum amount of stress. I blame this ALL on the colonoscopy ordeal.
Kaiser’s problem, as I keep being exposed to it (like a virus)is an inability to prioritize, and act swiftly on those priorities. Speaking of your priorities-I was called at 8:30 pm Monday night to reschedule yet another CT scan. The woman on the phone asked how next week looked for me. “Huh?” I said. “I thought this was an urgent priority.” “That’s the earliest we can take you sir,” she said. I felt like crying, this short conversation had me on the verge of an emotional breakdown. My wife whispered “What about another Kaiser somewhere else?” So I asked the lady on the phone, and after a few seconds she asked if I was close to Vacaville. I said yes, and she asked, “How about tomorrow?” I said fine and made the appt. (Do all your patients have to do all the problem solving in every situation?) Well, here it is, Friday, and no word yet!
And by the way, that tech also said the CT scan looked perfect! I did have to ask him to put gloves on during the execution of what I believe is called administering a “central line”...the number one reason and area for/of systemic infection likelihood. I may be wrong.
So, here it is Friday the 12th and no word, no call, no nothing. Another depressing weekend of wondering what could be wrong with me.
I finally received a call on Mon March 15th, from Dr. Cohen when he returned from vacation. He said the CT scan was in and he needed to see me asap. An appt. was set for 8:30am Wed the 17th. At the appt. he explained that I needed a biopsy because the problems he sees either stem from something to do with Cirrhosis or Cancer. At this time I asked about all the lower to mid abdominal pain and how did that have anything to do with my liver. To the best of my understanding his answer was that they are unrelated and I need to keep taking fiber so there’s no more blockage...Although I haven’t had any severe attacks in a couple of weeks, there is still pain (probably would be a lot worse if weren’t on pain meds already) and other symptoms. But clearly, in Dr. Cohen’s words, “This takes a back burner to the Liver issue.” Although I agree I don’t understand why both problems can’t be worked on simultaneously while giving priority to the Liver. Speaking of which, when I left the office Dr. Cohen said “someone” would be calling me to schedule an appt. for the biopsy, and if that hasn’t happened by Friday the 19th, to call him on Monday the 22nd.
Now this what I don’t understand, with all your modern technology, why can’t an appt. be made right then and there? Why does the ball always seem to land back in my court to follow-up and make sure things get done? It only seems that Kaiser Vallejo (in my limited experience) suffers from this follow through malady. Kaiser Martinez, and Dr. Yallagada, my new primary care location and doctor, said that I needed a Cardiologist appt. asap, and I was called later that day! Something which (the cardiologist appt.) Dr. Rubin neglected to do in the six or seven months that I saw him. Which actually surprised Dr. Yallagada because I had a heart attack Nov 11th 2008 and should have been assigned a Cardiologist immediately. In fact, it took a month of constant asking, emails and hassling, to get Rubin to schedule my yearly treadmill test! And then he had the cheek to say something like “Well, if it’ll make you feel better, and less stressed than I guess we could do one. But it’s really not called for.” I had spoken with the Cardiologist, Dr. Weiland, the Cardio-Surgeon who did my stent and angioplasty, and he said the treadmill test was imperative! Also Dr. Yallagada couldn’t understand why I was still on Plavix, a medication usually stopped after the first year of the heart attack.
Developments:
I saw a therapist outside of Kaiser because I was getting worried about some issues that started shortly after my colonoscopy trauma.
If you have ANY questions please call-
Hunter Austin