Topics (13) View all

Research experience

    • Jan 1989–
      Dec 1995
      Research: University of KwaZulu-Natal
      University of KwaZulu-Natal · Department of Paediatrics and Child Health
      Durban · South Africa
  • Teaching: I enjoy teaching undergraduate and postgraduate medical students. I have more than 30 years of teaching experience
  • Jan 1980
    Research: Rheumatic Heart Disease, Rotavirus Infections and Infantile Gastroenteritis, Use of Folic Acid in Infantile Diarrhoea, Asthma in Children, Juvenile Arthritis. I have more than 50 scientific publications in refereed journals and over 30 Congress Papers
    University of KwaZuluNatal · Dept of Paediatrics, Nelson Mandela School of Medicine, Durban · University of KwaZuluNatal
    Durban

Education

  • Jan 1974
    Colleges of Medicine of South Africa, plus University of Natal
    Fellowship in Paediatrics, plus fellowship in family Practice, plus Doctorate in Medicine (Research)
    South Africa · Durban
  • Jan 1974
    University of Natal
    Paediatrics & Child Health
    South Africa · Durban
  • Feb 1953–
    Dec 1958
    Witwatersrand
    Medicine · MB BCh
    South Africa · Johannesburg

Awards & achievements

  • Jun 1993
    Award: Long Service Award Certificate: Republic of South Africa; for 20 years' unbroken service
  • Jan 1986
    Grant: Medical Research Council of south Africa: Grant for Rotavirus Research
  • Jan 1985
    Grant: University of Natal Grant: for Gastroenteritis Research
  • Mar 1981
    Grant: Medical Research Council of South Africa: Grant for Rheumatic Fever research
  • Dec 1958
    Award: Craib Prize for Excellence in Medicine
  • Dec 1956
    Award: Cluver prize in Preventive Medicine: 1956

Other

Questions and Answers (11) View all

Publications (37) View all

  • Source
    Article: Immunogenicity and safety of a live attenuated varicella vaccine in healthy Indian children aged 9-24 months.
    [show abstract] [hide abstract]
    ABSTRACT: To investigate the safety of live attenuated varicella vaccine (Oka strain) and the optimal virus titre/dose required for immunogenicity in healthy South African children. Double-blind randomised clinical study using two different lots of varicella vaccine, each at two different titres. Subjects were randomly allocated to groups 1, 2, 3 and 4 to receive vaccine containing a mean virus titre of 10(4,5), 10(3,1), 10(3,9) and 10(2,7) PFUs per dose respectively. Clinical signs and symptoms were followed up for 42 days post-vaccination. Specific varicella antibodies were measured by an indirect immunofluorescence method in sera obtained on day 0 and day 42. City Health Clinic, Chatsworth, Durban. A total of 200 healthy 9-24-month-old children were vaccinated, of whom 189 (44,5%) completed the study. Pre- and post-vaccination varicella antibody levels. Adverse events following varicella vaccination. The vaccine was safe and well tolerated. No local symptoms were reported. Skin reactions were specifically solicited in this study: 21 reactions were reported in 8.5% (17/200) of children. Vesicles were reported in 2 vaccines (< or = 10 vesicles in both cases). One serious adverse event was reported: hospitalisation for bronchopneumonia on day 16 post-vaccination which resolved without sequelae. Around day 42 post-vaccination (range 35-63 days) all the 176 initially seronegative subjects had seroconverted for varicella antibodies. Post-vaccination geometric mean titres (GMTs) were 104.1, 66.2, 69.5 and 77.0 for groups 1-4 respectively. Six subjects who were initially seropositive maintained or increased their titres post-vaccination; 3 of the 6 showed a booster response (a > or = 4-fold increase from the pre-vaccination titre). Varicella vaccine was found to be safe, immunogenic and well tolerated. No difference in seroconversion rates or GMTs, either between groups receiving the two vaccine lots or between groups receiving the different titres of each lot, was shown.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 01/1996; 85(12):1295-8. · 2.04 Impact Factor
  • Article: The epidemiology of rotavirus infections: a global perspective.
    I E Haffejee
    [show abstract] [hide abstract]
    ABSTRACT: Rotavirus, which is the most common cause of infantile diarrhea worldwide, mainly affects infants between the ages of 6 and 24 months. Most infections in human newborns are mild or asymptomatic, due to the inherently attenuated nature of the "nursery" rotavirus strains. Adults are also sometimes affected, especially those in families with an infected child; the disease also occurs in closed adult communities. HIV-infected persons, travelers, or as a result of water-borne epidemics. Nosocomially acquired hospital infections add to morbidity and to the cost of hospitalization. A winter predominance of rotavirus diarrhea has been noted in temperate climates but not in tropical areas. Group A rotavirus infections are generally more common, but human infections with groups B and C have also been documented. The prevalence of serum antibodies is high during the neonatal period, but it declines sharply between the ages of 3 and 6 months, then rises steeply, peaking at approximately 2 years and remaining high into adulthood. Vaccines against rotavirus are currently under evaluation.
    Journal of Pediatric Gastroenterology and Nutrition 05/1995; 20(3):275-86. · 2.30 Impact Factor
  • Article: Rheumatic fever.
    I E Haffejee
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    ABSTRACT: The incidence of RF and RHD in the tropics remains high, with a high proportion of children suffering from carditis with the first attack. Severe, incapacitating haemodynamic disturbances occur early. Many patients are seen with established RHD at their first visit, and the default rate is high. Poverty, overcrowding, poor transport facilities, understaffed and overburdened clinics, and poor follow-up add to the problem. A genetic predisposition to develop RHD appears to be important in certain countries like India, Egypt and Turkey, but no work to show this has been done in black Africa. Secondary prophylaxis remains the most practical means of controlling the disease in the tropics. Compliance with long-term prophylaxis depends on organized and concerted efforts of physicians, other health personnel, parents, teachers, and the community.
    Baillière s Clinical Rheumatology 03/1995; 9(1):111-20.
  • Article: Child health in South Africa -- past, present and future.
    I E Haffejee
    Global child health news & review 02/1995; 3(1):18.
  • Article: Nuyritional management during acute infantile diarrhoea
    Haffejee I E
    [show abstract] [hide abstract]
    ABSTRACT: During an acute diarrhoeal episode, the infant should continue to be fed his or her normal feeds i. e. breast or cow's milk formula. If, however, diarrhoea persists, the stools should be tested first for reducing substances: a positive test is indicative of lactose intolerance in which case a lactose free formula can be substituted. The common practice of introducing soya-based lactose-free formula ab initio in all babies who have acute dirrhoeal disease without confirming the presence of lactose intolerance has no scietific basis and is to be deprecated
    Postgraduate Doctor (Africa). 01/1993; 15:8-10.

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