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Things to Know About Choosing a Thoracic Surgeon

Choosing a thoracic surgeon is an important decision. Patients should seek a doctor with significant experience in treating their condition and procedure. Surgery always carries risks, and understanding anticipated outcomes is essential. Ask your thoracic surgeon about your procedure’s success rates, recovery period, and long-term effects.

Know Your Options

Thoracic surgery is a surgical procedure that treats diseases of the lungs, trachea (tube connecting mouth to the stomach), esophagus (tube between the throat and chest), and the chest wall. These include emphysema, swallowing difficulties, gastroesophageal reflux disease, bronchiectasis, lung cancer and other malignancies, and congenital heart disease. Thoraciologists use either minimally invasive techniques or traditional open surgery. They also collaborate with a team of specialists, including pulmonologists, cardiologists, gastroenterologists, oncologists, and radiation oncologists.

When choosing a thoraciologist like Armen Parajian, you’ll want to consider their credentials, experience, outcomes and affiliated hospital quality. You’ll also want to determine if they participate in your insurance plan. In addition, you should request recommendations from your primary care physician or another medical expert. Be wary of online patient reviews that appear overly effusive, as these may need to reflect your surgeon’s practice accurately. 

Look for Credentials

Thoracic surgeons—cardiothoracic surgeons—operate on the lungs, major blood vessels inside the chest, and the bony structures that form and support the chest cavity. They treat lung cancer, esophageal diseases, and other conditions that affect the lungs and heart. Healthgrades offers information on the years a thoracic surgeon has been in practice, their surgical volume, and their procedure specialties. Use these data to determine how experienced your doctor is with the operation you need. You should also find out whether your thoracic surgeon is certified by the American Board of Surgery (ABS) or the American Board of Cardiothoracic Surgery (ABTS). The latter has more specific requirements for training. It would help if you also looked at the surgeon’s hospital affiliation and reputation to ensure you get top-notch care before, during, and after your thoracic surgery. Hospital quality is important because your nurse and other healthcare providers will work with you after the surgery.

Read Patient Reviews

Thoracic surgeons diagnose and treat diseases of the lungs, chest wall, diaphragm, esophagus, and mediastinum. They can specialize in cardiac, thoracic surgery or general thoracic surgery. Cardiac and thoracic surgeons focus on diseases of the heart and blood vessels, while general thoracic surgeons operate on infections in organs in the chest cavity. Once a patient is diagnosed with a condition such as lung cancer, the thoracic surgeon will plan the best course of treatment. It may include additional testing, a referral to another specialist or surgery. When choosing a thoraciologist, reading online reviews is a great way to learn more about how doctors treat their patients. However, some online review websites can be misleading, and it’s important to consider the overall experience of a physician rather than one or two positive or negative reviews.

Check the Surgeon’s Hospital Affiliation

The surgeon you choose is a critical part of your treatment. Any surgical … Read More..

Medical Device Certification Courses Lead and Developed by Industry Professionals

People in the medical device (MD) field should know by now that today’s 93/42/EEC medical device directive will be obsolete. It means that start-up planning to put devices will face challenges brought by the Medical Device Reporting. That is why product development plans need to include a detailed analysis of the life cycle phases of medical devices against the new Medical Device Reporting requirements.

It is imperative to realize what the term lifecycle means: all phases in the MD lifespan, from its conception to disposal and final decommissioning. That is why people need to think about the certification process during the concept development and initial brainstorming, as well as choosing the right regulatory route which will enable individuals a safe and strategical journey, from the initial brainstorming to disposal and final decommissioning.

What is EEC? Click this site for details.

What is the focus of the new Medical Device Reporting?

Like most regulations, its main purpose or focus is to allow safe and effective devices to enter and remain in the European market. The potential clinical dangers for users and patients should be reduced as far as possible until positive risk-benefit examinations can be demonstrated.

As a manufacturer of these devices, companies need to keep these things in mind at all times and make this their guide when developing their technical documentation. Listed below is a simple overview of the path that will generate solid and detailed technical documentation. These details will eventually lead to the CE-mark.

Visit for info about CE-marking.

Define its intended use

It is surprising how frequently a lot of manufacturers overlook this, but it is very important that they define the intended use of their device correctly. The Global Harmonization Task Force document defines the intended use as:

The object or item, intent of manufacturers when it comes to the use of their products, services, or processes are reflected in the company’s instructions, information, and specifications.

The definition of medical devices is given in Article Two of the MDR. Documentation of the intended use of the item and checking if it falls under the MD definition is very important. To be categorized as an MD, it shouldn’t achieve its primary intended action by immunological, metabolic, or pharmacological means, but maybe helped in its functions by all means.

This report brings clarity and stability to the categorization of washers, disinfectors, and sterilizers. Furthermore, certain product categories don’t intend medical uses as defined in Article Two but will fall in the scope of the said regulation.

Determine the right conformity assessment procedure

As mentioned above, the right risk classification plays a very important part in the medical device certification process; according to Article 53 of the reporting, the possible conformity assessment procedures with reference to the important Annex of the regulation. The manufacturer needs to choose the right procedure and properly implement it.

Define risk classifications

There are seven risk classes (I, Is, Im, Ir, IIa, III). These things are based on the risk and criticality … Read More..