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Paediatric Pulmonologist in delhi

Paediatric Pulmonologist in Delhi

In the dynamic landscape of child healthcare, paediatric pulmonologists play a pivotal role in ensuring the well-being of young ones. These specialized medical professionals are dedicated to diagnosing and treating respiratory issues in children, contributing significantly to overall pediatric health.

Role of Paediatric Pulmonologists

Paediatric pulmonologists are responsible for identifying and managing a range of respiratory problems in children, from common conditions like asthma to more complex cases such as congenital lung disorders. Their collaborative approach with other healthcare providers ensures comprehensive care for young patients.

Qualifications and Training

Becoming a paediatric pulmonologist requires a solid educational foundation in medicine, followed by specialised training in paediatric pulmonology. This ensures that these professionals are equipped with the knowledge and skills needed to address the unique challenges of pediatric respiratory health.

Common Respiratory Issues in Children

Children often face respiratory issues like asthma, bronchitis, and pneumonia. Paediatric pulmonologists specialise in understanding and treating these conditions, tailoring their approach to the specific needs of each child.

Paediatric Pulmonologist in Delhi

Advanced Diagnostic Techniques

Paediatric pulmonologists employ advanced diagnostic techniques, including pulmonary function tests and imaging studies, to accurately assess the respiratory health of their young patients. These tools aid in precise diagnosis and effective treatment planning.

Treatment Approaches

The treatment approaches vary depending on the nature and severity of the respiratory issue. Medications, respiratory therapies, and, in some cases, surgical interventions may be recommended to ensure the best possible outcome for the child.

Preventive Measures

Beyond treatment, paediatric pulmonologists emphasize the importance of preventive measures. This includes vaccinations and lifestyle modifications that can significantly reduce the risk of respiratory issues in children.

Choosing the Right Paediatric Pulmonologist

Parents seeking the services of a paediatric pulmonologist should conduct thorough research into the credentials of potential healthcare providers. Seeking referrals from pediatricians or other trusted sources can also guide families in making informed decisions.

Paediatric Pulmonology in Delhi

In the bustling city of Delhi, paediatric pulmonology has become an integral part of the healthcare system. With a growing awareness of the importance of specialized care for children with respiratory issues, the region boasts a commendable number of skilled and experienced paediatric pulmonologists.

Challenges in Paediatric Pulmonology

Despite the progress in the field, challenges persist. Limited awareness about paediatric pulmonology and uneven access to specialized care in certain areas pose hurdles for families seeking the best possible care for their children’s respiratory health.

Future Developments in Paediatric Pulmonology

The future of paediatric pulmonology holds promise, with ongoing advances in research and technology. These developments aim to further improve healthcare outcomes for children with respiratory issues, offering new and more effective treatment options.

Community Education and Outreach

Raising awareness about paediatric respiratory health is crucial. Community education programs and outreach initiatives help disseminate information about preventive measures and the importance of early intervention in respiratory issues.

Insurance and Financial Considerations

Understanding insurance coverage for paediatric pulmonology services is essential for families. Additionally, exploring financial assistance programs can provide support for those facing economic challenges while seeking specialized care for their children.


In conclusion, the role of paediatric pulmonologists in Delhi and beyond is indispensable in ensuring the respiratory health of the younger generation. Their dedication to diagnosis, treatment, and prevention contributes significantly to the overall well-being of children, offering them the opportunity for a healthy and fulfilling life.


Sarcoidosis: Causes, Symptoms, Diagnosis & Treatment

Sarcoidosis, a rare disease that triggers the formation of lumps or nodules known as granulomas, can affect various parts of the body, including the lungs, lymph nodes, skin, and eyes. This enigmatic condition, characterized by its diverse range of symptoms, demands a deeper understanding to navigate its complexities effectively.

What is Sarcoidosis?

Sarcoidosis manifests when the immune system goes into overdrive, creating granulomas. These granulomas, comprised of clustered white blood cells, can vary in size and location, leading to a spectrum of symptoms. From mild discomfort to severe manifestations, these granulomas are a hallmark of sarcoidosis. In some cases, they progress into fibrosis, resulting in permanent lung scarring.

The Anatomy of Granulomas:

Granulomas, the focal points of inflammation, consist of white blood cells enclosed within dense fibrous tissue. This encapsulation forms hard and lumpy nodules, contributing to the distinct characteristics of sarcoidosis. The body initiates this process to shield itself from perceived threats, demonstrating the intricate mechanisms of the immune system in action.

Affected Areas:

While granulomas can develop anywhere in the body, they predominantly affect the lungs and lymph nodes. Additionally, these inflammatory clusters may manifest visibly in the skin, eyes, or muscles, leading to specific and recognizable symptoms for accurate diagnosis and management.

Demographic Insights:

Sarcoidosis does not discriminate but shows a predilection for certain demographics. It is more prevalent in the Black population than in whites, and it affects individuals assigned female at birth slightly more than those assigned male at birth. Typically, sarcoidosis emerges between the ages of 25 and 40, painting a demographic picture that aids in early detection and targeted interventions.

Genetic Predisposition:

While sarcoidosis is not directly hereditary, individuals with first-degree biological relatives diagnosed with the condition face a higher risk. Genetic factors, intertwined with environmental triggers, underscore the importance of understanding one’s family medical history for proactive health management.

Prevalence and Rarity:

Sarcoidosis, by definition, is a rare disease, with fewer than 200,000 reported cases in the U.S. at any given time. Despite its rarity, the condition necessitates heightened awareness, comprehensive research, and support for affected individuals to improve diagnostic accuracy and develop effective treatment strategies.

Symptoms and Causes

What are the symptoms of sarcoidosis?

The symptoms of sarcoidosis depend on where in your body granulomas form. Most people with sarcoidosis have lung symptoms, but you can have symptoms in your skin, eyes, joints and almost anywhere else in your body. You may also have general feelings of being unwell or no symptoms at all.

General symptoms of sarcoidosis:

Joint pain
Muscle aches or weakness
Night sweats
Swollen lymph nodes
Unexplained weight loss
Kidney stones

Symptoms of sarcoidosis in your lungs:

Shortness of breath (dyspnea)
Chest pain

Symptoms of sarcoidosis in your eye:

Blurred vision or loss of vision (optic neuritis)
Eye pain
Red or swollen eyes (uveitis or conjunctivitis)
Sensitivity to light

Symptoms of sarcoidosis of your skin:

Growths under your skin around scars or tattoos
Light or dark patches of skin
Raised, reddish-purple sores or rash across your nose or cheeks (lupus pernio)
Red, tender bumps on your shins (erythema nodosum)

Symptoms of sarcoidosis of your heart:

Chest pain
Fluttering heartbeat (palpitations)
Irregular heartbeat (arrhythmia)
Heart failure
Shortness of breath

Symptoms of sarcoidosis of your nervous system:

Increased thirst or amounts of pee (Diabetes insipidus)
Weak or paralyzed facial muscles (Bell’s palsy)

Pulmonary sarcoidosis, a condition affecting the lungs, is often categorized into stages using the Siltzbach classification system. It’s essential to note that these stages do not necessarily indicate the severity of the condition, and individuals may not progress through each stage.

Instead, they are primarily based on the appearance of the lungs in chest X-rays and describe the locations of granulomas within the lungs and lymph nodes.

Stage 0: In this stage, chest X-rays do not reveal any signs of pulmonary sarcoidosis. Both the lungs and lymph nodes appear normal, providing no evidence of the condition’s presence.

Stage 1: Stage 1 involves the presence of granulomas exclusively within the lymph nodes. While these granulomas are present, they do not yet affect the lungs themselves.

Stage 2: At this stage, granulomas can be observed in both the lymph nodes and the lungs. This marks a progression from Stage 1, with the condition now impacting both areas.

Stage 3: In Stage 3, granulomas are found solely within the lungs. This stage signifies that the condition has become more localized and primarily affects the pulmonary region.

Stage 4: The final and irreversible stage is Stage 4. At this point, X-rays reveal pulmonary fibrosis, which denotes permanent scarring of the lungs. This stage represents a significant change in the condition’s nature, as it leads to lasting lung damage.

It’s important to understand that pulmonary sarcoidosis is dynamic, and individuals may move between these stages or experience the complete disappearance of granulomas. However, Stage 4 is the exception, as it indicates permanent and irreversible lung scarring.


What causes sarcoidosis?

Research suggests that sarcoidosis stems from a complex interplay of genetic predisposition and environmental factors, although its precise cause remains elusive. Studies suggest that certain individuals are more susceptible to an exaggerated immune response triggered by specific antigens, such as bacteria and viruses.

While the immune system is intricately involved, it’s crucial to note that sarcoidosis is not classified as an autoimmune disorder. The exact mechanisms underlying this condition continue to be a subject of ongoing scientific exploration and inquiry.

Since we don’t know for sure which combination of genes and triggers causes sarcoidosis, it’s impossible to predict who will get it.

Diagnosis & Treatment

How is sarcoidosis diagnosed?

Sarcoidosis diagnosis typically involves a physical exam, imaging like chest X-rays, and biopsy of suspected granulomas. Additional tests might be conducted to rule out similar conditions due to sarcoidosis’s resemblance to other illnesses.

How is sarcoidosis treated?

Sarcoidosis treatment focuses on symptom management and preventing organ damage. Medications that modify or suppress the immune system are commonly prescribed, tailored to the location of granulomas in the body. While there’s no specific cure, sarcoidosis often resolves spontaneously, and if symptoms are mild or non-life-threatening, immediate treatment might not be necessary. Patients work closely with healthcare providers to monitor symptoms and determine the most suitable course of action.

Complications/side effects of treatment

Corticosteroids can put you at increased risk of getting sick with an infectious disease and can cause a number of side effects, including:

Excessive weight gain
Diabetes in susceptible people
High blood pressure
Depression and emotional irritability
Skin bruising

For this reason, healthcare providers only recommend using medications to treat sarcoidosis if the benefits outweigh the risks.


How can I prevent sarcoidosis?

The cause of sarcoidosis prevention strategies remain elusive. However, adhering to prescribed medications under healthcare provider guidance can significantly decrease the risk of organ damage caused by granulomas. While the origins of sarcoidosis remain uncertain, proactive management is key to mitigating its potential impact.







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