Azathioprine and Cyclosporin ( an overview of two immunosuppressive medicines used to control my daughter’s eczema) from a parent’s point of view

I seem to be putting up a post quite infrequently off late but I hope to change that soon. In my defence I can only say that I have been enjoying myself too much and was quite tied up with my brother’s wedding late last month. It went off very smoothly and now the happy couple are spending quality time in Thailand.

Those of you who follow my blog and have read my earlier posts know what happened with my daughter due to the drug Azathioprine which was given to control her otherwise very severe eczema ( I have covered this in my post ….the tough get going Part II). I am pretty sure that other parents like me who have had to either put their child on this kind of immunosuppressive drug or have had to contemplate giving it go through the kind of jitters that I do from time to time.

I am very well aware about the reason and benefit of giving this medicine to my child without which leading a normal life for her would be almost impossible given the severity of her eczema at this point in time. But it does not stop me from thinking of all the possible side effects in the process of controlling her eczema especially given the life threatening consequences of giving her azathioprine last year. It is like having Hobson’s choice in this matter which means there is really no choice at all. I am sharing our experience with you in the hope that it may help you decide what is the best line of treatment for your child with the doctor’s support and bring a smile to your child’s face by making living with severe eczema bearable.

Hobson’s choice

IMG_1262By the time we gave Aiyana azathioprine last summer, we had exhausted all the other possibilities of various triggers like allergens, environmental causes like hot or cold temperatures, irritants like detergents amongst others. We also had an intensive moisturizing and bathing regimen to control her eczema but without much success. We had tried out all levels of topical cortisteroids and immunomdulators, wet wrapping therapies, phototherapy and oral steroids all of which are usually enough to manage mild-to-moderate atopic dermatitis. Although some mild cases of atopic dermatitis can be managed with emollients (creams, lotions and ointments) alone, there are some people who might require treatment with either topical corticosteroids or immunomodulators. When all these medicines and other measures to minimize environmental influences (elimination of allergens, dust mites, irritants like detergents and heat, perspiration and dry climates) fail, systemic options like oral steroids (prednisolone) and non-steroidal immunosuppressant agent such as azathioprinemethotrexate, ciclosporin or mycophenolate are often considered.

Azathioprine and cyclosporin- 2 different types of immunosppressant drugs

In Aiyana’s case azathioprine was prescribed by a leading pediatric dermatologist in London after doing a battery of tests including the enzyme test called TPMT (thiopurine methyltransferase). This enzyme plays a critical role in the chemical breakdown of azathioprine that is, in the way the body gets rid of this drug.  If a person is TPMT deficient, the effect of a particular dose of azathioprine will be exaggerated, and it could therefore become toxic to the bone marrow and hence the TPMT test is mandatory before giving this drug. Azathioprine has been in existence since the 1960s and was initially developed to prevent organ rejection and has been used for many years in the treatment of severe eczema. It is an immunosuppresant drug that is also known as antimetabolite. It hinders the growth of lymphocytes (a type of white blood cell) which are involved in inflammation associated with eczema. Azathioprine is given by mouth, usually once daily, and most often in the form of tablets of 25mg and 50mg.  It is also available in the liquid and allows more precise dosing for young children.

Cyclopsorin is another type of immunosuppressant drug which was also originally used to prevent organ rejection in transplant patients. It is in fact derived from a type of fungus. Even though the cause of Atopic dermatitis (eczema) is not completely understood and there is no cure as of now, what is known that immunological reactions occur in the skin of people with eczema and these are controlled by white blood cells (lymphocytes) that enter the skin from the blood. Cyclosporin decreases the production of chemical messengers which “switch on” these lymphocytes and thus dampen down strong allergic and immune reactions. It is available as capsules containing 10 mg, 25 mg, 50 mg and 100 mg of cyclosporin, however for children the liquid form is easier to give as a dose (one formulation is called Neoral®).

Side effects

Azathioprine has a very serious side effect and that is  ‘bone marrow suppression’, or ‘myelosuppression’.  The bone marrow is the site of production of the most important types of cell in the blood: the red cells (RBCs), the white cells (WBCs including neutrophils and lymphocytes) and platelets (important for blood clotting). White blood cells are critical in the body’s defence against infection, and if their numbers fall drastically (as did happen with my daughter),there will be a risk of potentially serious and even life threatening infection. Over the years it became clear that the patients who developed serious bone marrow suppression generally did so because they genetically inherited low TPMT activity. As mentioned earlier, this enzyme is essential in the chemical breakdown of azathioprine and thus has to be within a particular range for a person to be given this drug.

But no tests are really 100% foolproof as we saw in my daughter’s case. In spite of her test results being absolutely bang in the middle of the normal range and thus determining her dosage, within 3 weeks of putting her on this drug, she was hospitalised in the ICU with a life threatening infection due to severe “neutropenia” or an abnormally low number of neutrophils as a result of azathioprine induced bone marrow suppression. Neutrophils usually make up 50-70% of circulating white blood cells and serve as the primary defense against infections by destroying bacteria in the blood.

Hence, as in my daughter’s case, she developed life threatening infection and it was only the prompt and quality of medical attention, broad-based and potent antibiotics and antifungal medicines that saved her life. The dermatologist who had prescribed this drug had never seen this reaction in the many years that he has been successfully prescribing this drug to other children with such severe eczema. It became clear from my daughter’s reaction that there are other genetic variants that can be missed that can also make occasional patients susceptible to such severe adverse effects even while having the desired TPMT levels and these have possibly not been studied or accounted for.

Cyclosporin on the other hand is a potent immunosuppressant and starts to work very quickly (within 1–2 weeks) and the side effects of cyclosporin are almost all ‘dose-related’. Hence the side effects depends almost entirely on the dosage a person is taking although some people are more susceptible to the side effects than others. It cannot be given for long since the longer this drug is taken the more severe the side effects become. The main side effects of cyclosporin are hypertension (high blood pressure) and reduced efficiency of the kidneys (renal toxicity).  Blood pressure and kidney function need to be checked before treatment and monitored closely throughout treatment.

Regular and strict monitoring 

As with any such potent drugs, one has to be extremely particular about monitoring the relevant organ functions throughout the course of treatment. In Aiyana’s case, blood tests are a regular feature and she has almost come to terms with it. Initially I used to take her to one of the premier hospitals in Mumbai but in the past few months a phlebotomist has been coming home to collect her blood sample. He was referred by Aiyana’s pediatrician and is very gentle with her and it has made a world of difference as far as her blood collection is concerned especially since she has to go through this on a very regular basis.

In the case of azathioprine, the blood count levels become extremely important to monitor on a regular basis to check for bone marrow suppression. The medical protocol followed worldwide in the case of azathioprine is to undertake a blood test 3 weeks after starting treatment, then 12 weeks after starting treatment, and thereafter every 3 months if all the results are normal. However, as a learning from our traumatic experience, I would urge you to be on the side of caution and undertake the blood tests for your child every week for the first one or two months and then gradually space it out as per your doctor’s advice if there is no abnormal result. Such regular blood tests are a painful thing especially for a child but it is a necessary evil and must be carried out. These tests normally comprise a full blood count (mainly to check that white blood cell numbers – particularly neutrophil numbers – are not falling below normal levels), and liver function tests to ensure that the liver is not stressed.

When cyclosporin is given as the immunosuppressant, since kidney is one of the main organs which is affected, kidney function will need to be monitored regularly particularly the serum creatinine levels since any condition that impairs the function of the kidneys is likely to raise the creatinine level in the blood. It is thus important to recognize whether the treatment is leading to kidney dysfunction or not. The other important level to be monitored are the cholesterol levels since the reduced efficiency of the kidneys can also adversely affect the cholesterol levels leading to increased risk of heart disease.

Medicine that heals is not always sweet and caring words are not always pleasant

The main reason I chose to write about these 2 powerful drugs is that while there is a lot of information available about these drugs today on the net, it is not always easy to get the most relevant facts. One can get lost in too much of information all of which might not be completely relevant to a parent but more to a medical professional. Information about the plethora of side effects and adverse reactions from these drugs is also enough to scare away any parent from giving these to their children. I have tried to compile all the relevant and important information a parent should know before giving this drug to their child and bring it in one place.

The plan of these kind of treatments to control very severe eczema is, first, to achieve major improvement in the severity of a child’s eczema and then if possible to see it clear completely, though to achieve this may take several months or even years. We have had no choice but to use this treatment on our 7-year-old daughter and I hope that our experience and learnings come of use to other children afflicted with this condition in a severe form which usually affects their lives on a daily basis.  Of course, it is not easy for a seven-year old to take this medicine twice a day and undergo repeated blood tests, but as her caregiver I do not give her any option not too simply because we do not have any. We will have to evaluate her medication in the next few months and then go ahead with the next course of treatment based on her doctors’ recommendations.

I also wanted to share our experience with azathioprine so that other parents can take an informed decision while giving this drug and not repeat our mistake. One can simply never be too cautious where one’s child is concerned.

“Being a mother is learning about strengths you didn’t know you had, and dealing with fears you didn’t know existed”

20131213_180745Aiyana now lives an almost completely normal life with minimal itching and with not much outward physical manifestations of this skin condition which has had an adverse bearing on her social life in the past. I know we are all doing the best we can with the best possible treatments available at this point in time though I am forever in search of other better options that might come our way in the future.

Even then there are some moments that I am plagued by some doubts as to whether we have done everything that we could have to prevent her eczema from being so severe or something else we have not tried so far. I am so grateful for being given a second chance with her and I am sure all those who know her and are greeted by her sunny smiles would agree with me when I say there must be something we are doing “right” after all.

..the tough get going (Part 2)

It has been a very tough year for us and we went through the worst nightmare that any parent can ever face. But in the end, we have come out stronger as a family. And though we still have a long way to go, I am grateful for what we have and I know I will never give up this fight for my daughter’s chance at a happy, normal life.

(Please bear with me- this post is a bit long since there is a lot to cover and I do not want to break the continuity)

Family time!

Family time!

It was end April 2013 when we went for our 2 weeks trip to UK. We had a lovely time overall in London and Wales. The weather was amazing in London and we enjoyed the sun and outdoors. Aiyana was not happy that we took her to meet doctors in the middle of our holiday but she was a good sport about it. She was once again on oral steroids since mid April after being put off any medication since February. Her phototherapy had been going on as the solo treatment, but her skin suddenly started drying up very fast towards the middle of April. And within a few days her skin condition deteriorated rapidly and became absolutely dry and scaly and very itchy. She was immediately put back on oral steroids since that is the only thing that works for her immediately. Her skin condition was thus stabilised and was brought back under control.

In London, we took her to meet an experienced pediatric dermatologist at the well-known The Great Ormond street Hospital for children. We were extremely impressed with the hospital and its facilities catering exclusively to children. He gave us the confidence and hope that he would be able to manage her skin condition with the help of a immunosuppressive drug called Azathioprine. He has been using this immunosuppressive drug to control in children with severe eczema like Aiyana for the past 15 to 20 years. He assured us that it was able to control the eczema in most children and could be given to the children continuously for up to 2 years under strict monitoring. Also, once the drug was stopped after 2 years, the eczema did not come back in many of the children. They diligently carried out a series of tests on the children before starting the medication including an enzyme test called TPMT test.  Apart from the TPMT test, all her test results came back within a week and were all normal. Only her TPMT test result was left and that would take 3 weeks to come.

TPMT is an enzyme which is a critical element in determining the suitability of this drug for a patient and the optimum dosage,. One of the main side effects of Azathioprine is that it could very occasionally and unpredictably provoke adverse effects on the bone marrow. It was seen that patients on this drug who developed this serious and life threatening bone marrow suppression usually did so because they did not have this particular enzyma called  thiopurine methyltransferase (TPMT for short). This enzyme is essential in metabolising the drug in the body and its deficiency in the body could lead to toxicity in the bone marrow resulting in ‘bone marrow suppression’ or ‘myelosuppression’ at a particular dose of Azathioprine.

The bone marrow is the site of production of the most important types of cell in the blood: the red blood cells (RBC), the white blood cells (including neutrophils and lymphocytes) and platelets (important for blood clotting). Since White Blood Cells (WBC) are critical in the body’s fight against infection, any large fall in their numbers can lead to serious infection which can become life threatening. Hence, we had to wait for the test  results to come back before we could begin this medication under her local dermatologist’s care.

In the meantime, we also met a pediatric allergy specialist at London’s Guys’ and St Thomas’ Hospital. He gave us quite a few pointers on her allergies, but more importantly, we were able to finally rule out most of her allergies with a much more accurate (and painless) skin scratch and patch test. These tests confirmed that she was in fact, not allergic to wheat, sesame, soy, dairy and quite a few other allergens which had shown high IgE levels in her blood allergy or RAST test. I was really happy that finally we would be able to remove her dietary restrictions (especially gluten) almost immediately. He also mentioned a home rapid allergen for detection of house dust mite allergen called Ventia™ Rapid Test for Dust Mite Allergen  from US based INDOOR Biotechnologies. I have finally bought it online in the UK and it should get delivered soon. ( I will cover these other measures that I have taken at home in a separate post)

We then came back to India in mid May and waited for her TPMT results to come out. Finally they did, and her results were very much in the normal range. The doctors gave the go ahead for Azathioprine and the TPMT test helped determine the most effective dosage for Aiyana. As per the protocol, she was scheduled for a complete blood test for blood counts (WBC and RBC), liver and kidney functions 3 weeks after the start of the medication. Her oral steroids dosage had already been tapered down gradually and Azathriopine was started on the recommended dosage.

We started the medication and after a week or so I started noticing a darkening of the areas where her eczema was most prevalent inside of her knees, elbows and the back of her neck. Also, her nails became dark as well due to the drug. The doctors were not extremely concerned at that point in time since we were  expecting some changes due to the drug. In any case, we knew that her comprehensive blood test was scheduled for 19th of June and so continued her medication for almost 3 weeks.

And then all hell broke loose.

I remember vividly it was the 15th of June, Saturday when she started losing clumps of hair. And I mean clumps/big bunch of hair just literally falling out of her head every time she moved her head or touched it. I got horrified just looking at it but managed to hide the issue from her at that time. I got in touch with her pediatrician and dermatologist in Mumbai on Saturday and they both got concerned but none of us realised the extent of the problem since there were no other symptoms at that time. I could not reach her dermatologist in London since he was travelling and unfortunately for us even her pediatrician went on her scheduled break to London that week. Her blood tests were scheduled for Wednesday, 19th June, and we knew we would come to know if something was amiss very soon. It was a very upsetting time for all of us just seeing her hair fall out like that and keep on falling. Then she developed fever on Monday evening and since her own pediatrician was on leave, I consulted another doctor who gave her some medicine to control the fever. However, her fever shot up to 104/105 F the next night and we took her to see another pediatrician referred to us by a friend on Wednesday morning.

By this time we knew something was seriously wrong with her since her fever was hardly coming down and I was awake all night sponging her head and body to bring it down. But even at that time we did not realise how serious her condition was. Fortunately for us, the pediatrician took immediate action and sent us for a lot of tests to Breach Candy Hospital directly once we told him the medication she had been on and her very high fever. We did the tests and brought her back home only to be called by the doctor within a couple of hours and was asked to immediately admit her in the hospital. In retrospect, the pediatrician’s quick response was to save her life.

Our nightmare begins

Immediately after she was admitted to Breach Candy Hospital, she was taken to the Surgical ICU by the resident haemotologist since that was the only available place at that time which could take care of her by keeping her in isolation through “barrier nursing” (nursing with utmost precaution with respect to very high rsk of infection).  We came to know that she was suffering from “myelosuppression” which had led to “severe neutropenia”.  These words were to haunt us for the next 1 month and were the very same adverse side effects which were supposed to have been ruled out by the TPMT test. In other words, her bone marrow had effectively shut down and her body was unable to resist any infections and had caught a severe infection as a result. Her counts were

  • WBC- 290/μL                                                                                                                      (Normal range- 5,000-10,000 /μL)
  • Neotrophils (a component of WBC critical in fighting off infections)-  0.00(Normal range 40-75% of total WBC count)
  • Haemoglobin- 9.2 g/dL or  grams per 100 mls                                                       (Normal range- 13-18 g/dL)
  • Platelets- 54   (Unit: x10^3/uL) ;                                                                                   (Normal range – 140-440 units)

Aiyana was put on the strongest broad spectrum antibiotics and anti fungal medicines to help her fight the infection. Since her bone marrow had practically stopped working, she was totally dependent on the antibiotics and antifungal medicines to fight the infection for her.

Life in isolation

She was thus in isolation in the ICU and only the doctors and nurses were allowed to see her and they had to wear masks, gloves and gowns and take utmost precautions so that she did not catch further infections. Even Sudip and I were not allowed to be close to her initially and could only see her from a distance. At night however, they relented and let me sleep on a chair close to the door of the ICU cubicle in my mask, gloves and gown. Initially, we were allowed to go close to her only occasionally when she cried for us in pain or looked for us when she was awake. Most of the times in the beginning she was just too weary and ill from her little body fighting off the infection and the onslaught of medicines and injections and slept through most of the day. From then on for the next 2 weeks for my baby, each day was filled with injections for antibiotics, IV fluid injections, oral medications, an injection directly to the thigh bone to stimulate her bone marrow which was extremely painful. By this time, she had also completely lost her hair apart from a few tufts here and there.

Our life then

I cannot describe the pain and trauma she went through and I cannot describe in words my feelings as I came so close to losing her. My whole family and I just went through the days in a haze and I lost track of the days and other details of my everyday life. I knew only that I had to be strong for her and that I did not have the luxury of breaking down. The doctors tried their best put up a brave front but one could see that they were also extremely worried and not totally confident of the outcome. I truly came to know what the phrase “living one day at a time” meant. Each night I used to pray, hope, fight despair at various points in time sitting in the ICU that the next day would be a marginally better one. The pain and trauma that she had undergone last year was a cake walk compared to this. Through it all I tried to lift her spirits through reading her books, playing her favourite movies on the Ipad. Towards the end she was allowed to indulge in some painting and colouring activities to keep her occupied.

I will never forget the one question that she used to ask me every day and night ” mamma, when can I go home? Please take me home with you”. The days went by in a blur and there were 3 haemotologists working on her case apart from her pediatrician (who had come back to India by then), her dermatologist and all the resident pediatricians at Breach Candy Hospital. I will remain forever grateful to all the doctors and nurses who gave her a second lease of life.

Sudip and I managed to pull through for our daughter’s sake only with the help of our immediate families, friends and well wishers. We had a lot of friends and acquaintances who came forward to help us out by donating blood and platelets which we required on a regular basis. Our friends also kept my son company at home and gave me company at the hospital whenever required.

The turning point

Finally, after a nerve-wracking 2 weeks to the day she was admitted, came the turning point on her birthday on the 4th of July. My daughter’s birthday was the first day after she got admitted that the doctors declared her to be slowly on the road to recovery and out of danger. Thanks to the nursing staff, nutrition and diet team at the hospital who had arranged for a lovely birthday cake, we celebrated the good news. I think I started breathing once again that day and after that it was a very slow but definite road to recovery.

We used to all wait with bated breath for Aiyana’s full blood count every morning to monitor her recovery and  the doctors would adjust the medications accordingly.  She essentially had to undergo blood tests every day for 3 weeks that she was in the ICU and countless other injections including IV fluids. Later, the doctors were to say that it was my darling, brave Aiyana who gave them the hope and courage to fight this infection for her. My 7 year old daughter somehow managed to find the strength to greet us and her care givers with a smile and gave Sudip and I the strength to look for the silver lining when there were only dark clouds around. She was discharged with almost normal blood counts about 4 weeks after she was admitted.

IMG_1530

Life for us today

Today Aiyana has completely recovered from the ill effects of the drug but her eczema remains as severe. We had given her this medicine knowing the dangers since we have had no choice but to help control her extremely severe eczema that restricts her from leading a normal and comfortable life. But inspite of taking all due precautions and following due protocol our daughter’s life was put in extreme danger. As far as the doctors (in UK) have been able to guess, this happened due to a so far undiscovered gene that makes one highly vulnerable to this side effect. We will get her DNA testing done eventually to prevent this from happening to any other child.

If only we had been extra cautious and monitored this drug on a weekly basis instead of after 3 weeks as per the protocol for Azathioprine. But this is all in hindsight as we (including her doctors) truly did what we though was best for our child. As a parent, you can learn from our experience as we have done the hard way. You cannot be too cautious in monitoring any drug that you give your child no matter what the protocol is or what the doctor says.

Since her hospitalisation, her eczema was kept under control with the help of oral steroids. She has been on oral steroids for more than 6 months now and it needs to be tapered slowly since it has its own side effects. She has once again been put on the same immunosuppressant drug Cyclosporin (she took it well without showing any side effects) she was given last year to control her eczema which has remained as severe as before. However, I am continuously exploring other options which I have to take up very cautiously given our recent experience (but that is for another post and another day since this is one is already too long)

I do not give up hope that I will find a better way to control my daughter’s eczema and help her lead a normal life. I owe it to my brave little girl who has shown us what being strong is all about. You should take heart from our experience and continue to fight for your child.

After all, what does not break us makes us stronger.