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LIVER TRANSPLANT SURVIVAL RATE

LIVER TRANSPLANT SURVIVAL RATE

WHAT YOU NEED TO KNOW BEFORE AND AFTER SURGERY

A liver transplant is often the only hope for patients suffering from end-stage liver disease, acute liver failure, or certain types of liver cancer. It is one of the most complex yet life-saving procedures in modern medicine. Understandably, one of the most common concerns patients and their families express is;

“What is the liver transplant survival rate?”

In this blog, we’ll take a detailed look at liver transplant survival rates, what affects them, and how patients can significantly improve their outcomes. Whether you or a loved one is preparing for transplant surgery or exploring treatment options, understanding the statistics and influencing factors can help you make informed decisions and stay hopeful.

UNDERSTANDING LIVER TRANSPLANT SURVIVAL RATE

The liver transplant survival rate refers to the percentage of patients who continue to live after undergoing a liver transplant, typically measured at intervals of 1 year, 5 years, and 10 years. While outcomes can vary depending on individual health conditions, surgical expertise, and post-operative care, the overall survival rates have steadily improved in recent years due to advancements in surgical techniques, better immunosuppressive medications, and enhanced post-transplant care.

Average Global Survival Rates

1-year Survival Rate: 85% – 90%
5-year Survival Rate: 70% – 75%
10-year Survival Rate: 60% – 65%

These numbers reflect worldwide data but can vary from one region to another. For example, liver transplant centers in Pakistan, with experienced surgeons and multidisciplinary teams, are achieving survival rates comparable to international benchmarks.

WHAT INFLUENCES LIVER TRANSPLANT SURVIVAL RATE?

The survival rate after liver transplantation is influenced by a wide range of factors, many of which are within the patient’s control. Here’s a breakdown of the most critical aspects:

  • Underlying Liver Condition

The original disease that led to the liver failure plays a big role. Patients with chronic liver conditions like hepatitis B or C, fatty liver disease, or autoimmune hepatitis generally do well post-transplant. Those with liver cancer (especially hepatocellular carcinoma) also benefit, provided the cancer is diagnosed early and has not spread.

  • Patient’s Overall Health

Patients who are relatively stable, younger, and have fewer other illnesses, such as heart or kidney disease, tend to have a better liver transplant survival rate. Early referral and transplantation before the onset of multiple organ complications make a major difference.

  • Type of Transplant: Living vs. Deceased Donor

Interestingly, studies show that living donor liver transplant (LDLT) patients often experience slightly better survival rates than those receiving organs from deceased donors. This is because living donor surgery is often pre-planned, the liver is fresher, and the recipient is usually in better condition at the time of surgery.

  • Expertise of the Transplant Team

Survival outcomes are closely tied to the skill, experience, and support systems of the transplant team. At Pakistan Kidney and Liver Institute & Research Center (PKLI & RC), we follow int’l protocols, use advanced surgical tools, and provide 360-degree patient support, contributing to higher survival outcomes & fewer post-operative complications.

  • Post-Transplant Care & Patient Compliance

The transplant surgery is just the beginning. Long-term survival depends heavily on the patient’s commitment to follow-up care. This includes taking immunosuppressive medications daily, attending routine checkups, monitoring liver function, and maintaining a healthy lifestyle.

REALISTIC EXPECTATIONS VS. FEAR OF STATISTICS

While it’s important to understand liver transplant survival rate figures, it’s equally crucial to view them in the right context. Each percentage represents an average across thousands of patients with different backgrounds, ages, diseases, and lifestyles.

Rather than seeing survival rates as fixed numbers, consider them as starting points. With the right care, many patients live healthy, fulfilling lives for decades after their transplant. Infact, I have patients who are doing remarkably well, even 15 to 20 years post-transplant, enjoying normal family life and careers.

TIPS TO IMPROVE YOUR SURVIVAL AFTER A LIVER TRANSPLANT

Here are some simple yet powerful ways to enhance your long-term survival chances:

  1. Take Medications Without Fail

Immunosuppressive drugs prevent your body from rejecting the new liver. Skipping even a few doses can be dangerous.

  1. Follow Dietary Advice

Eat a balanced diet, avoid raw or undercooked foods, reduce salt, and limit sugar. A liver-friendly diet helps keep weight, blood pressure, and blood sugar in check.

  1. Avoid Infections

Post-transplant patients have a weaker immune system. Practice good hygiene, avoid crowded places during flu seasons, and keep up with vaccinations.

  1. Quit Smoking & Alcohol

Smoking narrows blood vessels and increases the risk of complications. Alcohol is extremely harmful post-transplant and should be completely avoided.

  1. Regular Checkups

Never skip follow-up visits. These appointments help your doctors detect any early signs of rejection, infection, or medication side effects.

HOPE BEYOND NUMBERS

For many patients, the decision to undergo a liver transplant is filled with anxiety. While the liver transplant survival rate can offer a sense of direction, it should not define your destiny. Every patient is unique, and many go on to exceed expectations with proper care, faith, and medical support.

At PKLI & RC, we don’t just focus on performing successful surgeries, we believe in building long-term success stories. From donor selection to recovery, from counseling to lifelong guidance, we are with our patients every step of the way.

CONCLUSION

In summary, the liver transplant survival rate has improved dramatically over the years, offering renewed hope to thousands of patients around the world. While statistics provide a helpful framework, the real outcome depends on a partnership between the medical team and the patient. With timely treatment, expert care, and patient dedication, survival after liver transplantation is not just possible, it’s often transformative.

If you or a loved one is considering a transplant, don’t let numbers discourage you. Focus on what you can control, and take that brave first step toward healing.

Prof. Faisal Dar (Sitara-e-Imtiaz)
D. Sc. (Honoris Causa) FCPS, FRCS, FEBTS
Dean, Pakistan Kidney & Liver Institute and Research Center

Appointment 📞 0307 5446668 | 0341 0543883 | 042 111 117 554

What if Liver Cysts turn into Tumor

What if Liver Cysts turn into Tumor?

 

Introduction

Liver cysts are fluid-filled sacs that develop within the liver. In most cases, these cysts are benign and don’t cause any symptoms or health issues. However, with the passage of time, there is a lingering concern and the possibility of liver cysts turning into tumors.

In this article, we’ll try to dig out the connection between liver cysts and cancerous tumors, the potential risks involved, the steps we can take for early detection of any possible development of tumor, and the cautions we can follow to prevent any such thing from taking cancerous shape.

What are Liver Cysts?

Liver cysts are fluid-filled sacs that appear on your liver. Initially, nearly all liver cysts are benign (noncancerous) and can vary in size from small, barely noticeable sacs to larger cysts that can be several inches in diameter. It is to be noted here that few cysts grow large enough to cause symptoms, but that doesn’t mean they are cancerous.

Besides, some liver cysts are also caused by an inherited disorder that may be treated through medication. Liver cysts are often detected incidentally during routine medical imaging tests, such as ultrasounds or CT scans, performed for unrelated health concerns.

Most liver cysts are classified into two types:

Simple Liver Cysts

Simple cysts are the most common type of liver cysts and typically don’t cause symptoms or any kind of complications. Simple liver cysts are usually benign and rarely develop into tumors.

Polycystic Liver Disease

This is a rare inherited condition where multiple cysts develop within the liver. While it can cause symptoms and may lead to liver enlargement, the risk of these cysts becoming cancerous is still relatively low. However, polycystic liver disease, if left untreated, can cause your liver to convert into liver cirrhosis.

What are the Risks of Liver Cysts Turning into Tumors

In most of the cases, the liver cysts remain non-cancerous and do not progress into tumors. However, there are some factors that may increase the risk of complications;

Size & Number of Cysts

Larger cysts, a higher number of cysts, and a longer history of cysts present in the liver may slightly elevate the risk of developing complications. Such complications do include the possibility of cysts becoming tumors.

Age

Liver cysts tend to become more common as you age. However, the risk of cysts turning into tumors remains relatively low.

Polycystic Liver Disease

Patients with polycystic liver disease are at a higher risk of developing complications due to the large number of cysts in their liver. However, the risk of developing tumors increases if you have Polycystic Liver Disease.

Caution & Screening

Although liver cysts rarely turn into tumors, it’s important to take precautions and remain proactive and cautious about your liver health.

Regular Check-ups

If you have liver cysts, make sure to schedule regular check-ups with your healthcare provider. They can monitor the size and number of cysts over time.

Healthy Lifestyle

Our first priority should be our focus on our health. Maintaining a healthy lifestyle, including a balanced diet, exercising regularly, and limiting alcohol consumption, can keep your liver in good shape.

Don’t Delay Treatment

In some cases, large or symptomatic liver cysts may require treatment. Treatment options may include drainage procedures or even surgical removal if necessary, and as per your healthcare practitioner’s recommendations.

Screening for Polycystic Liver Disease

If you have a family history of polycystic liver disease, make sure to get yourself screened regularly for genetic testing.

Conclusion

While there is a minimal risk of liver cysts turning into tumors, it’s crucial to approach this concern with accurate information and a proactive mindset. Most liver cysts remain harmless and benign throughout a person’s life. By maintaining regular communication with your healthcare provider and adopting a healthy lifestyle, you can reduce any potential risks and ensure the ongoing health of your liver. Remember, early detection and prompt medical attention can address any complications that may arise from liver cysts, providing you with peace of mind and optimal liver health.

Polycystic liver disease (PLD): Symptoms & Health Impact

What is polycystic liver disease?

Polycystic liver disease:

Polycystic liver disease (PLD) is a genetic disorder characterized by the growth of numerous cysts, or fluid-filled sacs, in the liver. These cysts can range in size from a few millimeters to more than 20 centimeters and can cause the liver to become enlarged and distorted.

PLD can occur in isolation, or it can be associated with other conditions such as polycystic kidney disease (PKD) or autosomal dominant polycystic kidney disease (ADPKD). In the latter case, PLD is often referred to as autosomal dominant polycystic liver disease (ADPLD).

What are the Symptoms of Polycystic Liver Disease?

Symptoms of Polycystic Liver Disease:

Many people with PLD have no symptoms, and the condition is often discovered incidentally during imaging tests performed for other reasons. However, as the cysts grow and the liver becomes enlarged, it can cause a range of symptoms, including:

Abdominal pain:

This is the most common symptom of PLD, and it can range from mild discomfort to severe, debilitating pain. The pain is often described as a dull ache in the upper right quadrant of the abdomen and may be worsened by eating or physical activity.

Abdominal swelling:

As the liver enlarges, it can cause the abdomen to swell or become distended. This may be noticeable as a bulge or protrusion in the belly.

Nausea and vomiting:

PLD can cause feelings of nausea and may lead to vomiting, especially after eating a large meal.

Jaundice:

In rare cases, PLD can cause jaundice, a yellowing of the skin and whites of the eyes. This occurs when the cysts compress the bile ducts in the liver, leading to a buildup of bilirubin (a waste product) in the blood.

Shortness of breath:

In very severe cases, PLD can cause the liver to push against the diaphragm (the muscle that separates the chest cavity from the abdomen), making it difficult to breathe.

How does Polycystic Liver Disease affect your overall health?

PLD can have a significant impact on a person’s overall health and quality of life, particularly as the cysts grow and the liver becomes more enlarged. Here are some ways that PLD can affect your health:

Decreased liver function:

As the cysts grow and the liver becomes more distorted, it can affect the liver’s ability to function properly. This can lead to a range of complications, including jaundice, ascites (fluid buildup in the abdomen), and liver failure.

Pain and discomfort:

As mentioned above, abdominal pain is a common symptom of PLD and can be quite severe. This can lead to decreased quality of life and limitations in daily activities.

Digestive problems:

PLD can cause digestive problems such as nausea, vomiting, and difficulty digesting food. This can lead to weight loss and malnutrition if left untreated.

Respiratory problems:

In severe cases, PLD can cause compression of the diaphragm, leading to difficulty breathing and respiratory distress.

Psychological impact:

Living with a chronic illness like PLD can be stressful and can take a toll on a person’s mental health. Many people with PLD report feelings of anxiety, depression, and isolation.

What is Treatment for Polycystic Liver Disease?

Treatment for Polycystic Liver Disease:

There is no cure for PLD, but treatment options are available to help manage symptoms and slow the growth of the cysts. Here are some of the treatment options that may be recommended:

Pain management:

Over-the-counter pain relievers like acetaminophen or ibuprofen may be recommended to help manage abdominal pain.

Polycystic liver disease (PLD) is a genetic disorder characterized by the growth of multiple cysts, or fluid-filled sacs, in the liver. These cysts can vary in size from a few millimeters to more than 20 centimeters and can cause the liver to become enlarged and distorted. PLD can occur alone, or it can be associated with other conditions such as polycystic kidney disease (PKD) or autosomal dominant polycystic kidney disease (ADPKD).

PLD affects both men and women equally, and it is estimated to affect between 1 in 1000 and 1 in 10000 people worldwide. It is usually diagnosed in adulthood, but it can occur at any age.

Causes of Polycystic Liver Disease:

PLD is a genetic disorder caused by mutations in one of several genes involved in regulating cell growth and division. The specific genes involved vary depending on the type of PLD. For example, mutations in the PRKCSH and SEC63 genes have been associated with autosomal dominant polycystic liver disease (ADPLD), while mutations in the PKD1 and PKD2 genes are associated

with polycystic kidney disease (PKD) and ADPKD.

The mutations in these genes cause an abnormal proliferation of cells in the liver, leading to the formation of cysts. The cysts grow over time and can eventually cause the liver to become enlarged and distorted.

 

Treatment Options:

Treatment options for PLD depend on the severity of the disease and the symptoms that a person is experiencing. In some cases, no treatment is necessary, and the disease can be managed through regular monitoring and lifestyle changes. However, in more severe cases, treatment may be necessary to manage symptoms, prevent complications, and improve quality of life

 

Here are some of the treatment options that may be recommended:

Lifestyle changes:

Making certain lifestyle changes can help manage PLD symptoms and prevent complications. For example, avoiding alcohol and caffeine, eating a healthy diet, and getting regular exercise can all be beneficial.

Pain management:

Pain is a common symptom of PLD, and pain management strategies may be recommended to help alleviate discomfort. Over-the-counter pain medications like acetaminophen or ibuprofen can help manage mild to moderate pain, while prescription pain medication may be necessary for more severe pain.

Drainage procedures: In some cases, cysts may need to be drained to alleviate pain or prevent complications. This can be done through a procedure called percutaneous aspiration or sclerotherapy, in which a needle is inserted into the cyst and the fluid is drained. This can be done under ultrasound guidance to ensure the needle is properly placed.

Surgery:

Surgery may be necessary to remove large cysts or to alleviate symptoms that are not responding to other treatments. There are several surgical options for PLD, including laparoscopic cyst fenestration, which involves creating a small opening in the cyst to drain it, or liver resection, which involves removing a portion of the liver containing cysts.

Liver transplant:

In very severe cases of PLD, a liver transplant may be necessary to replace the damaged liver with a healthy liver from a donor. This is typically reserved for cases in which the liver is failing and other treatments have been unsuccessful.

It’s important to note that PLD is a chronic condition, and there is currently no cure. Treatment is aimed at managing symptoms and preventing complications. Regular monitoring is important to ensure that the disease is not progressing and that any complications are caught early and treated appropriately.

In addition to these treatment options, there are several ongoing research studies aimed at developing new treatments for PLD. These include studies of new drugs that may help slow the growth of cysts, as well as studies of gene therapy and other novel approaches to treating the disease.

polycystic liver disease is a genetic disorder characterized by the growth of multiple cysts in the liver. While many people with PLD have no symptoms, the disease can cause abdominal pain, swelling, nausea, and other digestive problems as the cysts grow and the liver becomes enlarged.

While there is currently no cure for PLD, ongoing research is aimed at developing new treatments to help manage the disease and improve the quality of life for those living with it.

What is the survival rate of pancreatic cancer?

Aslamo Alicum sir I am Dr. Ali Hasan Radiology Specialist from Bahawalnagar.
Sir, I have three questions.

What is the survival rate of pancreatic cancer?

We read that the entire pancreas is not removed.

So I want to know that

What is the percentage survival rate after medication and surgery?

My second question is should it be corrected with medication or is it better to go for a liver transplant in the beginning? Some experts say that a liver transplant may be the best solution if the liver is headed for failure in the beginning.
Can it be treated medically for some time?
My third question is
Many slim people have also been found to suffer from fatty liver and it is also the case that many obese people do not suffer from fatty liver.
My question is that it is definitely linked to Leopard’s profile.

But what percentage does it measure that the cholesterol is high?

Sir, I have a friend who recently had dengue which started his ALT to rise.
Liver-related symptoms will not be found in the patient.
Will he need a protective agent to increase his platelets or not?

Thank you very much doctor I will try to explain it briefly.
Liver cancer is considered among the most dangerous cancers Unfortunately, 80 to 85 percent of patients are diagnosed with this cancer when they have advanced to stage four.
So in this case the chance of survival can be up to 3 months without chemotherapy and 9 months with chemo and up to one and half years at most.
Patients with early-stage liver cancer may have their liver removed.
In summary, it is dangerous cancer and is curable if diagnosed at an early stage.
Early diagnosis occurs in 10 to 15 percent of patients and surgical resection is the only ray of hope

Early stage means the cancer is limited to the pancreas and can be surgically removed.

 

Your second question was related to Bud Carrey Syndrome which is very common in Pakistan
There are three different types of treatment for this type of patient.
Patients with bud carriers eventually require liver transplantation

Most common liver disease

Most common liver disease

Most common liver disease:

Hepatitis A is the most common liver disease worldwide. The liver is an organ about the size of a football. It sits just under your rib cage on the right side of your abdomen. The liver is essential for digesting food and ridding your body of toxic substances. Liver disease can be inherited (genetic). Liver problems can also be caused by a variety of factors that damage the liver, such as viruses, alcohol use, and obesity.

Hepatitis A is the most common liver disease. Hepatitis A virus is a type of virus that attacks the liver. Human feces (poo) contain the virus, which is spread by infected food and water. However, it can also be spread by sharing needles and through unprotected sex, especially anal sex. Although complete recovery usually occurs without medical intervention, occasionally serious illness might occur. Those who are at higher risk of contracting the virus can acquire a vaccine.

Symptoms:

This most common liver disease can be contracted in many ways but some few reasons are listed below:

  • consuming food prepared by an infected person who hasn’t properly cleansed their hands
  • consuming contaminated water (including ice cubes)
  • eating shellfish caught in unclean water without proper cooking
  • drug injection using dirty needles
  • being in close quarters with an infected person
  • engaging in sexual activity with a carrier of the disease without protecting yourself with a condom or dental dam.

Some of the symptoms which can be observed when the person has hepatitis A are

  • symptoms similar to the flu, such as weakness, fever, and aches and pains
  • lack of hunger
  • experiencing symptoms of illness
  • diarrhea
  • Discomfort in the upper right quadrant of the abdomen (abdomen)
  • Weeds and poop that are dark in color and white in contrast (poo)
  • skin and eye yellowing (jaundice)
  • red, itchy, irritating patches on your skin.

Precautions:

Hepatitis A is the most common liver disease because people contract it without taking precautions but this disease can be avoided if taken necessary steps Washing your hands frequently, especially after using the restroom or before preparing or eating food, is one of the best ways to prevent the virus from spreading from person to person.

If the water from the tap isn’t safe to drink, you should boil it first before using it to brush your teeth or drink it. Additionally, you should peel and wash all of your fresh fruit and vegetables and stay away from meat and fish that is uncooked or undercooked.

When engaging in recreational drug use, it is possible to transmit hepatitis A to others through the sharing of contaminated needles and syringes; therefore, it is critical to always use fresh injecting equipment.

Treatment:

This disease is deadly if not taken precautions. This most common liver disease at this time has no treatment right at the moment. Getting plenty of rest, maintaining a healthy diet, and drinking lots of fluids are typical recommendations from medical professionals. It is possible that you will be provided painkillers as well as medication to assist with itching, nausea, or vomiting. Within one to two months, the majority of people will have made a full recovery You shouldn’t prepare food for other people or have sex until a healthcare practitioner advises you that you are no longer contagious, regardless of whether or not you are experiencing symptoms. You are immune to hepatitis A once you have recovered from it, which implies that you are unable to contract it again. However, it is still possible to get other types of hepatitis.

 

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