Stop trusting US medical staff to take charge of your record transfers between. The odds of this happening with zero errors are not in your favor. HIPPA means that all US citizens are entitled (whether insured or not) to all personal medical information. Because the current medical focus is on obtaining and coding records for insurance billing, but not on sending information between practices or you, the patient, you need to be proactive in this area.
Is it absurd that female cardiac patients have to research, follow up and micromanage (sub contract) their own complicated health care between doctors? Yes. It is the current state of medical culture at this time. Do yourself a big favor and get started building your paper trails if you haven't yet begun.
A few suggestions
1. Get into the habit of automatically requesting copies of each doctor visit (no matter what the specialty). If possible, ask at check-in. If not, request copies be mailed to your address. Faxes are ok, but far more likely to be sent haphazardly or appear illegible in critical areas. If your request is refused, ask for the refusal reason in written form. This is serious business. Follow up refusals with on-line reports of these incidents to the Attorney General in your state.
2. HIPPA means this is FEDERAL LAW and doctors cannot refuse a patient copy requests. Any medical facility that shows resistance to this request from this point on is a facility that you may want to consider distancing yourself from as quickly as possible. If they are resistant about record sharing that indicates overt patient-hostile atmosphere. Not where you want to get health care if you have other choices. Report these incidents to the Attorney General in your state. Even if you choose to go elsewhere, the women coming behind you may face revised office attitudes if they are audited by the state AG's office.
3. Make the time to organize your medical records in some fashion that makes sense to you...so you can easily retrieve even when alone, confused, under duress from medical symptoms and medication side effects. Do your best to take time every 6 months to revisit your medical files to ensure they are up to date and stacked/filed/stuffed/slung somewhere YOU are able to get to.
4. Take copies of any heart related surgical intervention descriptions (usually 1-4 pages), including event lab tests (blood, etc). Just enough info to hand over to each new doctor you see (no matter what their specialty, including dental). All cardiac events impact entire body. All your doctors should have access to this info BEFORE they proceed with treatment.
5. Hand your cardiac event description papers over as soon as your doctors walk into your exam space. That will pre-empt precious (expensive) wasted time and preclude dismissal of you as a serious cardiac risk patient. From that moment forward, this doctor will have upfront access to info that will effect the medications and treatments he/she prescribes.
Handing over this information will make your doctors decisions as safe and helpful as possible. They are free to use your copies to request doctor to doctor patient files transfers of the same thing you handed over, but it gives them a useful heads up....and a place to start.
6. Eventually, transparency of medical file info and transfer will be the norm....but in the meantime, remember that all your doctor has when entering your exam space is your person and possibly a sketchy written discription of your CURRENT complaint. YOU need to take responsibility to inject your extensive and most critical patient history records into the picture. Unless you do so, it is unlikely any of your physicians are taking the initiative to correspond or confer regarding your history and ongoing care. You need to be your own advocate. Start talking WHILE you hand over the heart issue documents. It's YOUR dime!
7. Do your best to override cultural training that makes you feel you must apologize for 'being an inconvenience' when speaking to a doctor. Do not apologize, do not minimize your actual symptoms, (docs are trained to listen for key words and start building a treatment/diagnostic tree....although this will possibly entail dismissal of the most distressing symptoms you are experiencing). You only have 5-11 minutes face time during an average visit, so take deep breaths, do your best to calm down and speak clearly in words that make sense to you.
8. The calmer you are able to remain (I know this can be extremely difficult), the better your chances of assessing the doctor's abilities and absorb clues as to how your symptoms are being interpreted and addressed. An easy going physician style can be reassuring and also deadly if your symptomology is being dismissed even while you are speaking. Do your best to keep eyes open and mind calm and alert for cues. If you find you are feeling in a defensive postition while describing your chest sensations, nausea, clamminess, etc....you may have already picked up this particular doctor is already dismissing what you are telling him/her and going instead to what they were taught in medical school (generally that females under 55-60 proclaiming cardiac symptoms are not at high risk of heart attack).
9. Keep searching for a heart doctor that feels like a good fit for you but do not expect female cardiologists to have different mindsets than male colleagues. Not at this time.
10. There is a possibility that in the not too distant future, something like universal health insurance will become a reality. This offers the implication that 'pre-existing' denials will disappear. It will always remain important to vigilantly request and obtain copies of your medical records. This is not the time to be leaving your cardiac/health care coordination to chance....especially in the event there are massive health care industry changes. Make the effort to obtain all your records now.



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