October 31, 2009
CUTTACK: Diagnosis and detection of blood disorders has taken a quantum jump in the State with the Clinical Haematology wing of the SCB Medical College and Hospital acquiring a state-of-the-art laboratory to conduct complicated tests.
The advanced facility is equipped with a fully automated capillary zone electrophoresis machine, fully automated five part cell counter and a fully automated coagulometer besides other instruments. It is all set to acquire a flow cytometer to carry out advanced tests for detection of critical blood diseases like cancer. It would be installed by the end of November.
The haematological laboratory billed to be the only of its kind facility in the State and able to conduct all kinds of examinations is being set up at an investment of Rs 1 crore by the State Health Department.
Head of Clinical Haematology Dr RK Jena said the facility would speed up tests and save people from the problems of having to send the samples outside the State for accurate diagnosis of complicated ailments.
The electropherosis machine would enable testing of thalassemia, sickle cell anemia, multiple myloma and other types of blood cancer with accuracy of almost 100 percent. Presently, samples were sent outside or done manually which had high error possibilities. The cell counter would undertake blood cell examination while coagulometer would detect bleeding disorders like haemophilia. The soon-to-be-installed flow cytometer would be used to diagnose blood cancers.
Blood diseases like sickle cell anemia, thalassemia are highly prevalent in Orissa while more than 70 percent of the population is estimated to be suffering from anemia. Besides, cancers of the blood are also on an alarming rise.
According to Dr Jena, the costs of the sophisticated tests would come down drastically. Sickle cell anemia, thalassemia tests would be done at around Rs 250 against Rs 1000 now.
October 31, 2009
Courtesy by: dailymirror.lk
A ward in the Thalassemia Centre at the Teaching Hospital in Kurunegala became the latest location where a vial containing an anti-biotic drug was found with a piece of glass.
When the medical staff got ready to administer the drug on the patients of the ward, the detection was made.
The nurse of the ward who detected the piece of glass in a vial containing Ampicillin had handed it over to the Chief Medical Officer of the Thalassemia Centre, Paediatrician Dr. Dayananda Bandara.
Dr. Bandara said that it was a very serious situation as the minute pieces of glass that could be present in the liquid drug could cause severe damage if it enters the blood stream and affect the heart, eyes, kidneys and the liver.
The possible coagulation blood around such a glass particle may block arteries and create severe heart conditions too, he said.
Dr. Bandara said that the Ministry of Health has been risking the lives of helpless patients by importing such low quality drugs. It is learnt that the drug was imported from India.
October 30, 2009
Courtesy by: timesofindia
RAJKOT: In an exemplary move, a philanthropist adopted 10 children suffering from thalassemia major and minor for a lifetime at a function here
on Thursday. Jagatsinh Jadeja will ensure regular blood transfusion of these children through out their lives.
“The major concern of the parents of a thalassemic child is regular blood transfusion to be done every two years. In order to relieve the parents of this burden, I decided to do my bit by taking responsibility of 10 children,” said Jadeja, former sarpanch of Ribada village.
Jadeja is also conducting a blood donation camp on November 3rd in the memory of his late brother Ramdevsinh Jadeja.
According to Gujarat chapter of Indian Red Cross Society, several government hospitals across the state are approached for adoption drive of thalassemia kids. Mostly, philanthropists in the memory of their deceased kith and kin go for such charity. “In the past nine years, there have been 18 blood donation camps organized especially for thalassemia patients,” said an official from the Red Cross Society.
October 30, 2009
Courtesy by: telegraphindia.com
Ten-year-old Ansila Abdul Aziz, a patient with thalassaemia from a village near Calicut in Kerala, was at the Congress headquarters today knocking on the corridors of power in Delhi to seek better medical treatment at home.
The Congress headquarters here had an unusual group of visitors today — about 30 children with chronic blood disorders and their parents and grandparents from the Malabar, seeking central intervention after years of agitation in vain in their state.
“Our children are suffering from thalassemia, haemophilia, sickle cell anaemia, and the medical college and hospital in our area (Calicut) does not have the right facilities for diagnosis or even treatment,” said Kareem Karassery, general convenor of the Blood Patients’ Protection Council from Mukkam, Calicut. Karassery lost his son to thalassemia two years ago.
A senior Congress official said he had never seen so many children throng the party headquarters. Some squatted on steel chairs, some played on the lawns, others looked on with quizzical eyes — while their parents pleaded for their future.
The council submitted a charter of demands at the Congress headquarters, seeking action from health minister Ghulam Nabi Azad. It wants a haematology department with specialists and infrastructure for the treatment of chronic blood disorders at the Calicut medical college hospital.
“Right now, patients have to travel all the way to the Christian Medical College, Vellore, for haematology services,” Karassery said.
The charter also seeks steps to prevent genetic blood disorders.
October 30, 2009
Courtesy by: twocircles.net
New Delhi: Chronic blood disorder patients and their parents from Kerala’s Malabar region today unsuccessfully tried to march towards the Indian Parliament to press the central government for their long pending demand of free and expert treatment to them whom the state government has so far neglected.
The protestors comprising women and children under the banner of Blood Patients’ Protection Council (BPPC) submitted a memorandum to the Union Minister for Health and Family Welfare Ghulam Nabi Azad demanding the government to provide free treatment to these patients suffering with deadly diseases like thalassemia, haemophilia sickle cell anemia, applastic anemia, leukemia etc.
BPPC has been fighting for better treatment to these patients of Malabar region for the last 15 years. The group has undertaken many agitations including a state secretariat march on February 28, 2001 with terminally ill patients demanding free and expert treatment from Calicut MCH. The Kerala Government has not shown interest to solve the problem. Now they have decided to take out a Parliament march.
Talking to TwoCircles.net Kareem Karassery, General Convener, BPPC, said: “For the last one and half decades we have been fighting for life saving drugs and expert treatment to these acute blood disorder patients but neither the state nor central government have so far heeded to our demand. So we have arrived here to highlight our issue at the national level.” More than 10,000 people are suffering from various blood disorders in Malabar region, he added.
The protestors have put 10 demands before the government. They include urgent prevention of genetic blood disorders and other birth disorders which are alarmingly growing Malabar area, setting up a health insurance for the complete treatment of acutely ill patients irrespective of their income or age limit, proper facilities for treatment of the related diseases at the MCH Calicut.
October 30, 2009
Courtesy by: ameinfo.com
The DHA will celebrate healthcare quality week from the 1st to the 4th of November, 2009. All DHA hospitals and speciality centres will take part in this event.
Dr Mohammad Al Olama, CEO of the Hospital Services Sector initiated this celebration to promote the importance of achieving improved patient care outcomes and healthcare delivery systems. This year’s theme is, “Patient Safety, Our Priority”
Al Wasl, Dubai Hospital, Rashid Hospital, DHA Airport clinic, the Thalassemia centre and the Harvard-affiliated Joslin Diabetes Centre will take part in this event.
On the 4th of November, the DHA will hold a seminar as well as conduct other awareness activities at the Rashid Medical Library Auditorium to discuss this year’s theme- “Patient Safety, Our Priority.”
October 30, 2009
Courtesy by: thenational.ae
A handbook listing the pre-nuptial medical tests and check-ups that people have to take before entering into a marriage has been jointly released by the Ministry of Health and the Marriage Fund Corporation.
The booklet is part of a series of projects put together by the two government institutions after Dr Hanif Hassan Ali, Minister of Health, and Dr Maitha al Shamsi, Minister of State and chairwoman of the Marriage Fund, signed a memorandum of understanding in June. Sixty-thousand copies of the book will be distributed through both ministries and also made available in clinics and medical centres, the government news agency WAM reported yesterday.
It will also be given to new couples applying for a Marriage Fund.
Dr Mahmoud Fekri, the executive director for health policy affairs, said the handbook was in line with a personal affairs law of 2005, Article 27, in which it is stated that medical tests are compulsory before marriage for anyone wanting to wed in the UAE.
The medical report must be presented before a marriage contract can be finalised and both parties have to be clear of all the diseases listed in the handbook.
These include inherited blood disorders such as beta thalassemia and sickle-cell anaemia; contagious diseases; and sexually transmitted diseases such as HIV and hepatitis B and C.
In March 2008, the MoH began providing services for pre-marriage tests through nine medical centres across the UAE.