Top Tweets for #DILATED
🫀 🧬 The largest genetic and #MRI study carried out to date rules out the existence of a heart condition: left ventricular hypertrabeculation, which is not associated with a poorer prognosis in patients with #dilated cardiomyopathy.
This research was carried out by a team from @CNIC_CARDIO in collaboration with a wide-ranging international network of hospitals and research centres, led by @dr_pavia, head of the CNIC’s hereditary cardiomyopathies group and a cardiologist at @HospiPtaHierro and the CIBERCV (@ciberisciii).
🔗 DOI: doi:10.1161/CIRCULATIONAHA.125.078536. #OpenAccess in @CircAHA
📰 Read the full news article here: https://t.co/MJEsaXpkOd
#CNIC #CardiovascularResearch #Science
bender is bending me over and fucking me raw #dilated
#ClinicalPearl
#Dilated #nailfold #capillaries
list 3+ diseases that can have this finding
#Diagnosis in 1 #picture
Hint
pt has #Raynaud’s
🔥 #HFA @escardio scientific statement :
Future development of arrhythmogenic risk scores in patients with #HeartFailure & inherited #Dilated #CMP.
Cardiologists that manage #DCM cannot count on a validated score for the definition of #SCD risk ☠️ ⚡️
Integration of:
🧬 Genetic background & -omics
🩻 Imaging and ⚡️ Electro-physiological characterization
👨🏻⚕️ 🩺 Clinical data & competing needs
Will validate new scores 🍀
@HFUAcademy 🫀 https://t.co/0dFvFm9NeT
@ESC_Journals @HanCardiomd @AmrAbdin10
@BorianiGiuseppe @gcfmd @glimongelli @DrRajivsankar @KTamirisaMD @drraviele @JBauersachsMD @MicheleEmdin @stefanocarugo @ShelleyZieroth @mvaduganathan @SJGreene_md
@DrMarthaGulati @IacopoOlivotto
@AndrewJSauer
@HFA_President
https://t.co/F7IOCQHz2j
🗞️ Future development of arrhythmogenic risk scores in patients with #HeartFailure & inherited dilated cardiomyopathy.
A scientific statement of the #HFA of @escardio
@ESC_Journals @GiuseppeGalati_
@AmrAbdin10 @HanCardiomd
@HFA_President
https://t.co/BF7LQEPOrP
Impact of Truncating Variants in Titin on Dilated Cardiomyopathy Risk: The Role of Genetic and Lifestyle Factors!
https://t.co/lGwzxuR8ol
#dilated #cardiomyopathy #titin #genetic #cardiotwitter #EHJ @ESC_journals @escardio
📢Call for Papers! 📷#RCM
💪Seeking Submissions on "Dilated Cardiomyopathy"!
✍️Submit now: https://t.co/75xceqqV1j
📩 Contact: [email protected]
#Dilated #Cardiomyopathy #Cardiovascular
#recommendedpaper #MustRead #IndustryTrends #InsightfulRead
Today's recommended article is as follows:🥂
Title: #Hypertrophic, #Dilated, and #Arrhythmogenic Cardiomyopathy: Where Are We? 🚟
Check it out:🎰
https://t.co/QbRpXvxJXh
@MDPIOpenAccess @MDPIBiologySubj
#Dilated #Cardiomyopathy (DCM) in #Dobermans: A Serious Concern
Dilated Cardiomyopathy (#DCM) is a significant heart disease that sadly affects #Doberman Pinschers more than many other dog breeds.
It's a condition where the heart muscle becomes thin and weakened, particularly the left ventricle, which is responsible for pumping blood to the rest of the body. This weakening leads to an enlarged heart that can't effectively circulate blood.
Key Aspects of DCM in Dobermans:
* Hereditary Nature: DCM in Dobermans is primarily an inherited condition. Several genetic variants have been identified that increase the risk of developing the disease. The exact mode of inheritance is complex and can involve multiple genes.
* Prevalence: The prevalence of DCM in Dobermans is high, with some estimates suggesting that over 50% of the breed may be affected.
* Age of Onset: While DCM can develop at various ages, it typically manifests in middle-aged to older Dobermans, often between 4 and 10 years old. However, it can occur earlier or later in some individuals.
* Clinical Signs: The signs of DCM can be subtle in the early stages. As the disease progresses, dogs may exhibit:
* Exercise intolerance and lethargy
* Coughing, especially at night or after exercise
* Difficulty breathing or increased respiratory rate
* Weakness or fainting episodes
* Swollen abdomen due to fluid buildup (ascites)
* Weight loss
* Sudden death due to cardiac arrhythmias (irregular heartbeats) is also a significant concern, sometimes occurring with no prior warning signs.
* Diagnosis: Diagnosing DCM typically involves a thorough cardiac examination by a veterinarian, including:
* Echocardiogram: An ultrasound of the heart to assess its size, shape, and function.
* Electrocardiogram (ECG): To evaluate the electrical activity of the heart and detect arrhythmias.
* Holter Monitor: A portable ECG that records the heart's rhythm over 24 hours to identify intermittent arrhythmias.
* Genetic Testing: Blood or cheek swab tests are available to identify specific genetic mutations associated with DCM in Dobermans. However, it's important to note that not all Dobermans with these mutations will develop the disease (incomplete penetrance), and some dogs with DCM may not have the known genetic markers.
* Cardiac Biomarkers: Blood tests for substances like NT-proBNP and Troponin I can provide additional information about heart health.
* Treatment: Currently, there is no cure for DCM. Treatment focuses on managing the symptoms, slowing the progression of the disease, and improving the dog's quality of life. This often involves medications such as:
* ACE inhibitors: To help widen blood vessels and reduce the heart's workload.
* Diuretics: To help reduce fluid buildup.
* Pimobendan: To improve the heart muscle's contractility.
* Anti-arrhythmic medications: To control irregular heartbeats.
* Prognosis: The prognosis for Dobermans diagnosed with DCM varies. Some dogs may live for several months to a year or more with medication, while others may succumb to the disease more quickly, especially if sudden death due to arrhythmia occurs.
* Breeding Considerations: Due to the hereditary nature of DCM, it is crucial to carefully consider breeding practices. Genetic testing can help identify dogs at higher risk, and regular cardiac screening (echocardiograms and Holter monitoring) is recommended for breeding Dobermans, ideally starting around 3 years of age and continuing annually.
In conclusion, DCM is a serious and prevalent heart condition in Doberman Pinschers. Early detection through regular screening and responsible breeding practices are vital in managing this disease and aiming to improve the health and longevity of the breed.
If you own a Doberman, discussing the risk of DCM and appropriate screening measures with your veterinarian is highly recommended.
Title: Prognostic Value of #QRS Duration in Patients with #Dilated #Cardiomyopathy According to Left Ventricular Ejection Fraction
#DCM #LVEF #electrocardiography #RCMjournal
Text Link: https://t.co/4ZCezG4AH5
Lecture Update in Cardiology - Dilated Cardiomyopathy Part 1 & 2 by Dr. S. Booma on the RAAONLINE App.
Android: https://t.co/fSlaHVoEbl
IOS: https://t.co/oJAMS4dkMC
Contact: +91-9994994266
#raaonline #freelecture #medicalstudent #medicaleducation #dilated #cardiomyopathy
@Janetbirdope What device do you use to look closer?
Have I...
a) been to the hospital for eye tests?
b) just watched @SpursOfficial defend a set-piece?
#dilated
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