Wednesday, 25 December 2024

Transfusion Related Acute Lung Injury : Introduction & Mechanism

 Transfusion Related Acute Lung Injury :


The cause of TRALI is currently not fully understood. 80–85% of cases are thought to be immune mediated.


 Antibodies directed toward human leukocyte antigens (HLA) or human neutrophil antigens (HNA) have been implicated, with transfused antibodies shown to bind antigens expressed on pulmonary endothelial cells to initiate acute inflammation in the lungs.


 Women who are multiparous (have carried more than one pregnancy to viable gestational age) develop these antibodies through exposure to fetal blood; transfusion of blood components obtained from these donors is thought to carry a higher risk of inducing immune-mediated TRALI.


Previous transfusion or transplantation can also lead to donor sensitization. 


To be at risk of TRALI via this mechanism, the blood recipient must express the specific HLA or neutrophil receptors to which the implicated donor has formed antibodies. 


A two-hit hypothesis has been suggested wherein pre-existing pulmonary pathology (i.e., the first-hit) leads to localization of neutrophils to the pulmonary microvasculature. 


The second hit occurs when the aforementioned antibodies are transfused and attach to and activate neutrophils, leading to release of cytokines and vasoactive substances that induce non-cardiac pulmonary edema.


A proposed mechanism for non-antibody-mediated TRALI involves the accumulation of bioactive lipids in stored blood components (red cells, platelets, or plasma) that are capable of priming neutrophils.


TRALI is typically associated with plasma products such as fresh frozen plasma. 


TRALI can also occur in recipients of packed red blood cells, whether adult or pediatric patients.


Due to the higher risk of TRALI resulting from donations by females, the AABB (formerly the American Association of Blood Banks) has recommended that those blood components with a high volume of plasma not be used for transfusion, but for further processing into other therapeutic products.


 To mitigate the risk of TRALI, female donors are excluded from fresh frozen plasma donation in Germany as of 2009 if they have a history of pregnancy and there are no HLA/HNA screening results available, which has resulted in a significant reduction of TRALI reports.




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Sarcomere : Structure and Function


A sarcomere is the fundamental unit of striated muscles, such as skeletal and cardiac muscles, that is responsible for muscle contraction and performance. Sarcomeres are made up of many parallel thin actin filaments and thick myosin filaments, and are arranged in a stacked pattern throughout muscle tissue. 

Here are some key facts about sarcomeres:

Structure

Sarcomeres are arranged between two Z-lines, and contain an M-band and an elastic filament system made of titin. 

Function

Sarcomeres generate force and bear loads. The interaction between actin and myosin proteins is the basis of how sarcomeres shorten, which causes muscles to change length. 

Size

In vertebrate skeletal muscle, a sarcomere's resting length is about 2.5 millimeters. 

Number

A single muscle cell can contain thousands of sarcomeres. 

Disease

Understanding the molecular structure of sarcomeres can help us understand their role in health and disease. For example, the M-band is a shock absorber in contracting muscles, and its dysfunction can contribute to muscle disease.






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Friday, 20 December 2024

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Severe Combined Immune Deficiency Syndrome:

 Severe Combined Immune Deficiency Syndrome:


SCID is a rare, inherited disorder that affects the development and function of white blood cells. 


It's characterized by a deficiency of T and B cell development and function, which makes people with SCID highly susceptible to infections. 


SCID is also known as the “bubble boy disease” or “boy in the bubble” syndrome. 


This is due to the publicity surrounding David Vetter, a boy with X-linked SCID who lived in a germ-free plastic bubble for 12 years.


Management:


Gene therapy can be used to treat severe combined immunodeficiency (SCID) by correcting the root cause of the disease.


 Gene therapy involves: 


Inserting healthy human genes into a patient's stem cells.


Washing the virus from the cells.


Transplanting the corrected cells back into the body.


The corrected cells divide and proliferate, passing on the normal gene copies to all the blood cells. 


Gene therapy has been successful in treating children with XSCID and ADA deficiency SCID. 


However, some treatments and trials have been halted due to concerns over the safety of viral vectors. 


Other treatments for SCID include: 


Bone marrow transplantation, 


Enzyme therapy, 


Avoiding live vaccines, 


Antimicrobial prophylaxis, and 


Isolation to prevent catching an infection.


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Sunday, 15 December 2024

Porphyria Cutanea Tarda

 Porphyria cutanea tarda :


It results from underactivity of the enzyme uroporphyrinogen decarboxylase, which leads to accumulation of porphyrins in the liver. 


Liver disease is common. 


About 35% of people develop cirrhosis and 7 to 24% develop liver cancer.


Symptoms of Porphyria:


The acute (hepatic) porphyrias are characterized by episodes of abdominal pain (the most common symptom), constipation and other gastrointestinal symptoms.


Photosensitivity leading to pain immediately upon exposure to sunlight (e.g. EPP) or blistering and fragility of the skin in areas exposed to sunlight is seen in Porphyria cutanea tarda. 


How is PCT diagnosed?


 Diagnosisof (PCT) relies on the identification of characteristic symptoms, a comprehensive patient history, and a thorough clinical evaluation involving specialized tests.


Diagnosis is established by finding substantial increases in porphyrins in urine or plasma and excluding other blistering cutaneous porphyrias.


What is the drug of choice for porphyria cutanea tarda? :


Porphyria cutanea tarda may be treated by simply avoiding the precipitating factors.


 However, phlebotomy and hydroxychloroquine are both effective in achieving biochemical and clinical remission.

Saturday, 14 December 2024

Primary Vs Secondary Data

 Primary Data Vs Secondary Data :


The main difference between primary and secondary data is that primary data is original information collected by a researcher for a specific purpose, while secondary data is information that has already been collected by someone else.


Primary data:


Original information gathered by the researcher for a specific purpose. 


Primary data is unique, first-hand, and from an original data source. 


Examples of primary data include interviews, original artwork, and personal narratives. 


Secondary data :


Information that has already been collected by someone else. 


Secondary data is usually gathered from published sources, such as statistical synopses, census records, and government reports. 


Researchers use secondary data to gain a broad overview of a topic, understand how other researchers have approached it, and support or contrast their arguments with other researchers' ideas. 


However, there are some limitations to using secondary data, including:


The quality of the secondary sources can affect the validity of the data.


The information may not fit the same boundaries as the primary data.


The data may address some issues but not others.

Monday, 4 November 2024

تاريخ الحالة رجل يبلغ من العمر 45 عامًا يعاني من ألم في الجانب الأيسر من الصدر ودوار وخوف لمدة يوم واحد






تاريخ الحالة

رجل يبلغ من العمر 45 عامًا يعاني من ألم في الجانب الأيسر من الصدر ودوخة وخوف لمدة يوم واحد.



يدخن 10 سجائر يوميًا وهو مصاب بالسكري أيضًا، ولكنه غير متوافق مع أدويته وتقديره الغذائي



عند الفحص، يكون ضغط دمه 100/60، ومعدل ضربات القلب حوالي 56 نبضة في الدقيقة، وتشبع الأكسجين 92 بالمائة.



يظهر تخطيط القلب الخاص به أدناه:



أ. ما هي النتائج التي توصل إليها تخطيط القلب؟

ب. ما هو التشخيص الأرجح؟

ج- ما هي أسباب هذه الحالة؟

د. ما هي إدارة هذه الحالة؟



حقوق الطبع والنشر (الصورة والنص) محفوظة للمؤلف.


 


بيانات مجهولة المصدر، تم أخذ الموافقة. 




الإجابات

أ. نتائج تخطيط كهربية القلب:



بطء القلب .

فترات PR متفاوتة وفترات R-R.

تغيرات إقفارية منتشرة على شكل اكتئاب مقطع ST.

تفكك AV كامل، مع معدلات أذينية وبطينية مستقلة.




ب. كتلة القلب الكاملة على الأرجح بسبب مرض القلب الإقفاري المنتشر.


في حالة إحصار القلب الكامل، يكون هناك غياب تام للتوصيل الأذيني البطيني، مع عدم وصول أي من النبضات فوق البطينية إلى البطينين.


يتم الحفاظ على إيقاع الإرواء عن طريق إيقاع الهروب المفصلي أو البطيني.


 وبدلاً من ذلك، قد يعاني المريض من توقف البطين مما يؤدي إلى الإغماء (إذا كان منتهيًا ذاتيًا) أو الموت القلبي المفاجئ (إذا استمر لفترة طويلة).


كتلة القلب الكاملة هي في الأساس نقطة النهاية لأي من كتلة Mobitz I أو Mobitz II AV

قد يكون ذلك بسبب التعب التدريجي للخلايا العقدية الأذينية البطينية وفقًا لموبيتز I (على سبيل المثال، ثانوي لزيادة النغمة المبهمة في المرحلة الحادة من احتشاء عضلة القلب السفلي).


بدلا من ذلك، قد يكون ذلك بسبب بداية مفاجئة لفشل التوصيل الكامل في جميع أنحاء نظام هيس-بوركينجي، وفقا لموبيتز الثاني. يمكن أن يكون هذا ثانويًا لاحتشاء الحاجز في احتشاء العضلة القلبية الأمامي الحاد، أو نتيجة لتطور مرض الجهاز الموصل الذي يسبب كتلة ثلاثية الحويصلات الحقيقية.


من المرجح أن يستجيب الأول للأتروبين وله تشخيص عام أفضل.

ج- الأسباب


الأسباب هي نفسها بالنسبة لإحصار القلب من الدرجة الثانية لموبيتز I وMobitz II. أهم المسببات المرضية هي:


احتشاء عضلة القلب السفلي.


أدوية حاصرات العقدية AV (مثل حاصرات قنوات الكالسيوم، حاصرات بيتا، الديجوكسين).


انحطاط مجهول السبب في الجهاز الموصل (مرض لينيجري أو ليف)، مما يسبب كتلة ثلاثية الحويصلات الحقيقية.


التشخيص التفريقي:


لا ينبغي الخلط بين إحصار القلب الكامل وبين:


إحصار AV عالي الدرجة: نوع من إحصار القلب الشديد من الدرجة الثانية مع معدل بطيني بطيء للغاية ولكن لا تزال هناك بعض الأدلة على التوصيل AV في بعض الأحيان.

تفكك AV: يشير هذا المصطلح فقط إلى حدوث انقباضات أذينية وبطينية مستقلة وقد يكون سببها كيانات أخرى غير كتلة القلب الكاملة (على سبيل المثال، "تفكك التداخل" بسبب وجود إيقاع بطيني مثل AIVR أو VT).

د- الإدارة 

إحصار القلب الكامل، والمعروف أيضًا بإحصار الأذيني البطيني من الدرجة الثالثة (AV)، هو حالة طبية طارئة تتطلب علاجًا فوريًا.

 تتضمن إدارة كتلة القلب الكاملة ما يلي: 

النقل السريع: يجب نقل المرضى إلى أقرب منشأة وتلقي دعم الحياة المتقدم (ACLS) مع مراقبة القلب المستمرة. 

تقييم الأعراض والعلامات الحيوية: ابحث عن علامات ضعف التروية المحيطية. 

تحديد مستوى الكتلة: يعتمد العلاج على مستوى الكتلة. 

سحب الأدوية المسببة: أوقف أي أدوية قد تسبب أو تؤدي إلى تفاقم إحصار القلب.

السرعة: السرعة عبر الجلد هي العلاج المفضل للمرضى الذين يعانون من الأعراض. إذا لم ينجح ذلك، فقد تكون هناك حاجة إلى جهاز تنظيم ضربات القلب عبر الوريد. 

 جهاز تنظيم ضربات القلب الدائم أو ICD: سيحتاج معظم المرضى إلى جهاز تنظيم ضربات القلب الدائم أو جهاز مزيل الرجفان ومقوم نظم القلب القابل للزرع (ICD) إذا لم يكن من الممكن علاج إحصار القلب بطريقة أخرى. 

 الأدوية المضادة لاضطراب نظم القلب: يمكن أن تساعد هذه الأدوية في منع نظم القلب غير الطبيعية. 


دراسة المتابعة: يمكن إجراء دراسة متابعة للتأكد من أن الدواء يعمل بشكل صحيح.


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Case History A 45 year old man presents with 1 day history of left sided chest pain, Dizziness and apprehension.

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Case History

A 45 year old man presents with 1 day history of left sided chest pain, Dizziness and apprehension.


He is smokes 10 cigarettes per day and is Diabetic as well, however not compliant with his medications and dietary discretion


On examination, his Blood pressure is 100/60, Heart rate is around 56 beats per minute and Oxygen saturation is 92 percent.


His ECG is shown below :


A. What are the findings in the ECG?

B. What is the most likely Diagnosis?

C. What are the causes of this condition?

D. What is the management of this condition?


Copyrights (Image and Text)reserved with Author.


Anonymized Data, Consent taken.





Answers

A. ECG Findings :


Bradycardia .
Varying PR intervals and R-R Intervals .
Diffuse Ischaemic changes in the form of ST segment depression.
Complete AV dissociation, with independent atrial and ventricular rates.


B. Complete Heart block most likely due to diffuse Ischaemic heart Disease.

In complete heart block, there is complete absence of AV conduction, with none of the supraventricular impulses conducted to the ventricles.

The perfusing rhythm is maintained by junctional or ventricular escape rhythm.

Alternatively, the patient may suffer ventricular standstill leading to syncope (if self-terminating) or sudden cardiac death (if prolonged).

Complete heart block is essentially the end point of either Mobitz I or Mobitz II AV block
It may be due to progressive fatigue of AV nodal cells as per Mobitz I (e.g. secondary to increased vagal tone in the acute phase of an inferior MI).

Alternatively, it may be due to sudden onset of complete conduction failure throughout the His-Purkinje system, as per Mobitz II. This can be secondary to septal infarction in acute anterior MI, or as a result of progression of conducting system disease causing true trifascicular block.

The former is more likely to respond to atropine and has a better overall prognosis.

C. Causes

The causes are the same as for Mobitz I and Mobitz II second degree heart block. The most important aetiologies are:

Inferior myocardial infarction.

AV-nodal blocking drugs (e.g. calcium-channel blockers, beta-blockers, digoxin).

Idiopathic degeneration of the conducting system (Lenegre’s or Lev’s disease), causing true trifascicular block.

Differential diagnosis:


Complete heart block should not be confused with:

High grade AV block: A type of severe second degree heart block with a very slow ventricular rate but still some evidence of occasional AV conduction.

AV dissociation: This term indicates only the occurrence of independent atrial and ventricular contractions and may be caused by entities other than complete heart block (e.g. “interference-dissociation” due to the presence of a ventricular rhythm such as AIVR or VT).


D. Management 

Complete heart block, also known as third-degree atrioventricular (AV) block, is a medical emergency that requires immediate treatment.


 Management of complete heart block includes: 

 

Rapid transport: Patients should be transported to the nearest facility and receive advanced life support (ACLS) with continuous cardiac monitoring. 

 

Assess symptoms and vital signs: Look for signs of compromised peripheral perfusion. 

 

Determine the level of the block: Treatment depends on the level of the block. 

 

Withdraw causative medications: Stop any medications that may be causing or aggravating the heart block. 

 

Pacing: Transcutaneous pacing is the preferred treatment for symptomatic patients. If that doesn't work, a transvenous pacemaker may be needed. 

 

Permanent pacemaker or ICD: Most patients will need a permanent pacemaker or an implantable cardioverter-defibrillator (ICD) if the heart block can't be treated otherwise. 

 

Anti-arrhythmic drugs: These drugs can help prevent abnormal heart rhythms. 

 

Follow-up study: A follow-up study may be performed to ensure the medication is working properly.


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Wednesday, 17 July 2024

Pulmonary Hypertension : German Version : Causes, Clinical Features , Complications and Management

 

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