RVV
Forum Newbies
Offline

I Love YaBB 2!
Posts: 3
|
PART 1
Dear RLR, I have been reading posts on this forum for a number of months. I would like to express my gratitude and appreciation for the work you have been doing in helping people cope with their anxiety, panic and arrhythmias. Regrettably, there very few doctors out there who are willing to take extra time and effort to alleviate the fear and anxiety of patients suffering from PVC’s and PAC’s .
I am a 24 year old male, who is in otherwise relatively good health, who developed PVC after a severe flue in August of 2010. I first noticed my pulse skip a beat after a heavy meal. Of course, I was concerned to about that incident, to say the least. I got an appointment with a Cardiologist and ran several diagnostic tests. My ECG was normal, with the exception of an IRBBB, which my doctor told me is considered to be normal and of no prognostic significance. My ECHO was normal, and my heart did well on a stress test, no PVC’s, with good exercises tolerance. My 48 hour Holter showed 530 Premature Ventricular Contractions and 10 Premature Supraventricular Contractions. I was surprised by the number, as I only felt 5 or 6 of them during that period of time. I asked my doctor if my symptoms might have been caused by a damage the virus (mild localized myocarditis?) caused to my heart (minor fibrosis) or its neurotoxic effects (damage to the Cardiac branch of the CNS). The doctor though that I never had myocarditis, and he hypothesized that my ectopic activity was caused by an overactive sympathetic nervous system (enhanced automaticity). However, he failed to explain to me as to why my SNS became overactive and what can be done to stabilize it. He even suggested that I always had PVCs and was never aware of them. However, that’s not true, since I wore a Holter Monitor when I was 20 (had it done when I complained about persistence chess tightness, which turned out to be muscle injury) and it recorded perfect sinus rhythm for 48 hours, no PVCs or PACs. My doctor didn’t really no what to tell me, so he said that people with PVCs have the same life expectancy as the general population and that I should go home and enjoy life.
I was no satisfied with his answer, nor did I believe that PVCs were innocent. After some research on the internet, I found several studies that clearly demonstrate that PVC, in ABSENCE of identifiable heart disease, do carry a negative prognosis. The first study I would like to mention is: “Prognostic Significance of PVCS and Resting Heart Rate” done by Stanford University Medical Center (Engel, et al.) in 2007.
After analyzing 2-minute ECG strips of over 45,000 individuals and following them for average of 5.5 years, the study came to a conclusion: “The presence of any PVC on a single ECG is a powerful predictor of all-cause and cardiovascular mortality. The presence of multiple or complex PVCs was not a significantly better predictor although there was a trend towards worse prognosis in patients with complex forms. Regression analysis demonstrates that heart rate is a significant and independent predictor of the presence of PVCs. Our findings support the hypothesis that activation of the sympathetic nervous system is an important factor in the genesis of PVCs and ventricular arrhythmias. The presence of elevated heart rate is a significant prognostic factor and the combination of increased heart rate PVCs dramatically increases mortality.”
In fact the study demonstrated that presence of PVCs doubles your cardiovascular mortality, even if PVCs happen at a low resting heart rate (presumably vegally induced).
The second study I would like to mention is “Relation of Atrial and/or Ventricular Premature Complexes on a Two-Minute Rhythm Strip to the Risk of Sudden Cardiac Death (the Atherosclerosis Risk in Communities [ARIC] Study)” 2011. This study monitored 14,574 subjects with normal ECG for 15 years. After analyzing the data they came to a conclusion: “Participants with PVC were 2 times as likely to have Sudden Cardiac Death (hazard ratio [HR] 2.09, 95% confidence interval [CI] 1.22 to 3.56) compared to those without PVC. Presence of PAC was not significantly associated with SCD (HR 1.15, 95% CI 0.56 to 2.39). Compared to subjects without PVC and PAC, risk of SCD in subjects with PVC and PAC was significantly increased (HR 6.39, 95% CI 2.58 to 15.84). In conclusion, our study shows that subjects with PVCs are significantly more likely to die from SCD, despite not having any known history of cardiovascular disease. This effect appears to be additive when PACs occur concurrently.” In fact having both PVCs and PACs increases your risk of suffering Sudden Cardiac Death by 600 percent!
And finally the last study: "Premature Ventricular Complexes and the Risk of Incident Stroke: The Atherosclerosis Risk In Communities (ARIC) Study." It monitored 14,000 people for 15 years, and came to conclusions that: “Frequent PVCs are associated with risk of incident stroke in participants free of hypertension and diabetes. This suggests that PVCs may contribute to atrioventricular remodeling or may be a risk marker for incident stroke, particularly embolic stroke.” Their data demonstrated that people with PVCs, who have no heart disease have double the risk of suffering a stroke, than the ones who don’t. Also, people who have PVCs and PACs are a lot more likely to develop A-Fib in the future.
The above mentioned studies clearly demonstrate that PVCs are not harmless, even when are found in individuals without structural heart disease. On the contrary, PVC are a significant risk factor for Sudden Cardiac Death and Stroke. People with PVCs and no heart disease have a significantly higher overall mortality than people without these arrhythmias. Hopefully, these studies will attract some attention to what once was thought of as ‘benign’ arrhythmias and lead to more research and development of treatments for enhanced abnormal cardiac automaticity.
|