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384 Obituary EDITH JOAN MILLAR M.B.Durh., F.F.A. R.C.S. Dr Millar, a former senior consultant ansesthesist to the Newcastle regional cardiothoracic surgical service, died on July 21 at the age of 68. She graduated from Durham University in 1932 and spent most of her career as an anxsthetist in thoracic surgery. With Dr Philip Ayre she was involved in the early thoracic oper- ations in the North East of England, and, in 1940, she cooper- ated with the late Mr George Mason in establishing a small thoracic surgical unit for battle casualties at Stannington Hos ’- pital. She was concerned in the creation of the regional centre at Shotley Bridge General Hospital in 1943, and later she pioneered the development of cardiopulmonary bypass for open-heart surgery at Shotley Bridge. She was president of the North of England Society of Anaesthetists in 1953-54. E. A. C. and J. A. G. H. write: "The development of thoracic surgery in the North of Eng- land could not have progressed so smoothly without her un- flagging loyalty and wise judgment on clinical matters. Her organising ability, her dedication to team work, her skill in anxsthesia, in diagnostic procedures, and in pre and post oper- ative care earned the profound respect of her colleagues. Up to the day of her retirement, although she had by then built up an excellent team of younger colleagues, she insisted on tak- ing a full and unvarying share of operating lists and emer- gency duties both for surgery and in the intensive-care unit. Apart from her work she will always be remembered by count- less visitors to the ’clinic’ at Shotley Bridge and by her profes- sional colleagues throughout the North of England for her un- failing kindness and consideration." LORD PLATT OF GRINDLEFORD H. T. N. S. sends this further tribute: "I was privileged to work with Robert Platt in the depart- ment of medicine when he was in Manchester, and I saw him at close quarters, perhaps in an unusual light, from the view- point of a general practitioner. He had asked me to take over the follow-up care of his large collection of hypertensives, who, in 1954, could be offered effective treatment for the first time. When we published a joint paper in The Lancet in 1956, I little realised how unusual it was to be: a future P.R.C.P., writing with a general practitioner. It was his interest in, and care of the patient as an individual that was immediately apparent. He knew them all by name, and I was introduced personally to each one, whom he had hitherto seen himself in his room at the Infirmary. So keen was he on the care of the whole per- son that he paid many a visit to general practices, including mine in Cheshire, to see how they worked. Always with some original thought about a problem, and often laced with his puckish sense of humour, he would sit through whole sur- geries. He was as interested in the short cuts as in the attention to detail and investigation in general practice. A kind, warm man with breadth of vision and an incredible knack of getting to the core of a problem, or seeing a completely different angle. Above all, his patients loved him." " Dr A. C. STANLEY SMITH, who served for over fifty years as a medical missionary in Uganda, Rwanda, and Burundi, died on Aug. 1. Dr CALVIN WELLS, a distinguished authority on palxopath- ology, died on July 31. Notes and News OF MUTANT MICE AND MONITORS ONE of the most exciting recent advances in genetic research in Britain has been the discovery, by Dr R. Gardner and Dr C. E. Graham of the zoology department at Oxford University, that teratocarcinoma cells maintained in vivo or in vitro can, when injected into early mouse embryos, take part in normal development and give rise to various tissues, including germ cells. This discovery, reported by a subcommittee of the Medi- cal Research Council appointed to review the state of clinical genetics in the U.K.,’ could perhaps lead to an explanation of how malignancy can be modified; it may also mean that new mouse models can be created for specific inborn errors of metabolism, by the incorporation of tumour cells selected in vitro for particular metabolic defects. The mouse is probably the most widely used mammalian model in biomedical research, and the subcommittee suggests that a centre for breeding and maintaining mutant mice, of which over 400 strains have so far been described, is now a pressing need in genetic research. Many of the more specialised genetically marked strains are at present obtainable only from a laboratory in the U.S.A. A central cell bank for tumour cells, mutants, and hybrids would also be valuable, but it would be very expensive to set up and run, and the subcommittee sug- gests that extra financial support for the few laboratories that already have experience of producing certain kinds of cells would be a useful first step towards the establishment of such a centre. On the clinical side, the subcommittee emphasises the need for monitoring systems to provide feedback about the effective- ness of genetic services offered to the public. A national regis- ter of amniocenteses, for instance, could be used to assess the reliability of prenatal diagnosis and the safety of amniocentesis and would enable the incidence of fetal abnormality in various categories of pregnancy to be determined. Prospective studies of genetic counselling would show whether the service is reach- ing all social classes, whether the clients understand the advice given, and whether they act upon it. An assessment of this kind might also reveal a need to give information about other ser- vices, such as family planning. A major challenge to genetic counsellors is how to advise patients of reproductive age who have been successfully treated for Hodgkin’s disease or lym- phoblastic leukaemia with multiple chemotherapy and radia- tion. Not all will be made infertile by their treatment, but it is not yet possible to say what risk the fertile patients run of producing a malformed fetus or whether the risk diminishes with increasing time after completion of chemotherapy. Early assessment based on a well-designed monitoring system would clearly be valuable. PAYMENTS TO THE VACCINE-DAMAGED THE scheme for vaccine-damage payments2 will provide for £ 10 000 tax-free for persons who have, since July 5, 1948, suf- fered severe damage as a result of vaccination (under routine public policy vaccination programmes) against diphtheria, tetanus, whooping-cough, poliomyelitis, measles, rubella (also when given to women of childbearing age), tuberculosis (B.C.G.), and smallpox (up to July 31, 1971). The criterion for payment will be disablement due to vaccine damage assessed at 80% or more, according to the established rules for indus- trial injuries disablement benefit, and the receipt of attendance or mobility allowance for conditions which could be attributed to vaccine damage will be accepted as evidence of severe damage. These payments will not prejudice the rights of those 1. Review of Clinical Genetics. A Report by the M.R.C. Subcommittee to Review Clinical Genetics, 1978. 2. See Lancet, 1978, i, 1028, 1056.

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384

Obituary

EDITH JOAN MILLARM.B.Durh., F.F.A. R.C.S.

Dr Millar, a former senior consultant ansesthesist tothe Newcastle regional cardiothoracic surgical service,died on July 21 at the age of 68.

She graduated from Durham University in 1932 and spentmost of her career as an anxsthetist in thoracic surgery. WithDr Philip Ayre she was involved in the early thoracic oper-ations in the North East of England, and, in 1940, she cooper-ated with the late Mr George Mason in establishing a smallthoracic surgical unit for battle casualties at Stannington Hos ’-pital. She was concerned in the creation of the regional centreat Shotley Bridge General Hospital in 1943, and later shepioneered the development of cardiopulmonary bypass foropen-heart surgery at Shotley Bridge. She was president of theNorth of England Society of Anaesthetists in 1953-54.

E. A. C. and J. A. G. H. write:"The development of thoracic surgery in the North of Eng-

land could not have progressed so smoothly without her un-flagging loyalty and wise judgment on clinical matters. Herorganising ability, her dedication to team work, her skill inanxsthesia, in diagnostic procedures, and in pre and post oper-ative care earned the profound respect of her colleagues. Upto the day of her retirement, although she had by then builtup an excellent team of younger colleagues, she insisted on tak-ing a full and unvarying share of operating lists and emer-gency duties both for surgery and in the intensive-care unit.

Apart from her work she will always be remembered by count-less visitors to the ’clinic’ at Shotley Bridge and by her profes-sional colleagues throughout the North of England for her un-failing kindness and consideration."

LORD PLATT OF GRINDLEFORD

H. T. N. S. sends this further tribute:

"I was privileged to work with Robert Platt in the depart-ment of medicine when he was in Manchester, and I saw himat close quarters, perhaps in an unusual light, from the view-point of a general practitioner. He had asked me to take overthe follow-up care of his large collection of hypertensives, who,in 1954, could be offered effective treatment for the first time.When we published a joint paper in The Lancet in 1956, I littlerealised how unusual it was to be: a future P.R.C.P., writingwith a general practitioner. It was his interest in, and care ofthe patient as an individual that was immediately apparent.He knew them all by name, and I was introduced personallyto each one, whom he had hitherto seen himself in his roomat the Infirmary. So keen was he on the care of the whole per-son that he paid many a visit to general practices, includingmine in Cheshire, to see how they worked. Always with someoriginal thought about a problem, and often laced with hispuckish sense of humour, he would sit through whole sur-geries. He was as interested in the short cuts as in the attentionto detail and investigation in general practice. A kind, warmman with breadth of vision and an incredible knack of gettingto the core of a problem, or seeing a completely different angle.Above all, his patients loved him."

"

Dr A. C. STANLEY SMITH, who served for over fifty years asa medical missionary in Uganda, Rwanda, and Burundi, diedon Aug. 1.

Dr CALVIN WELLS, a distinguished authority on palxopath-ology, died on July 31.

Notes and News

OF MUTANT MICE AND MONITORS

ONE of the most exciting recent advances in genetic researchin Britain has been the discovery, by Dr R. Gardner and DrC. E. Graham of the zoology department at Oxford University,that teratocarcinoma cells maintained in vivo or in vitro can,when injected into early mouse embryos, take part in normaldevelopment and give rise to various tissues, including germcells. This discovery, reported by a subcommittee of the Medi-cal Research Council appointed to review the state of clinicalgenetics in the U.K.,’ could perhaps lead to an explanation ofhow malignancy can be modified; it may also mean that newmouse models can be created for specific inborn errors ofmetabolism, by the incorporation of tumour cells selected invitro for particular metabolic defects.The mouse is probably the most widely used mammalian

model in biomedical research, and the subcommittee suggeststhat a centre for breeding and maintaining mutant mice, ofwhich over 400 strains have so far been described, is now apressing need in genetic research. Many of the more specialisedgenetically marked strains are at present obtainable only froma laboratory in the U.S.A. A central cell bank for tumour cells,mutants, and hybrids would also be valuable, but it would bevery expensive to set up and run, and the subcommittee sug-gests that extra financial support for the few laboratories thatalready have experience of producing certain kinds of cellswould be a useful first step towards the establishment of sucha centre.

On the clinical side, the subcommittee emphasises the needfor monitoring systems to provide feedback about the effective-ness of genetic services offered to the public. A national regis-ter of amniocenteses, for instance, could be used to assess thereliability of prenatal diagnosis and the safety of amniocentesisand would enable the incidence of fetal abnormality in variouscategories of pregnancy to be determined. Prospective studiesof genetic counselling would show whether the service is reach-ing all social classes, whether the clients understand the advicegiven, and whether they act upon it. An assessment of this kindmight also reveal a need to give information about other ser-vices, such as family planning. A major challenge to geneticcounsellors is how to advise patients of reproductive age whohave been successfully treated for Hodgkin’s disease or lym-phoblastic leukaemia with multiple chemotherapy and radia-tion. Not all will be made infertile by their treatment, but itis not yet possible to say what risk the fertile patients run ofproducing a malformed fetus or whether the risk diminisheswith increasing time after completion of chemotherapy. Earlyassessment based on a well-designed monitoring system wouldclearly be valuable.

PAYMENTS TO THE VACCINE-DAMAGED

THE scheme for vaccine-damage payments2 will provide for£ 10 000 tax-free for persons who have, since July 5, 1948, suf-fered severe damage as a result of vaccination (under routinepublic policy vaccination programmes) against diphtheria,tetanus, whooping-cough, poliomyelitis, measles, rubella (alsowhen given to women of childbearing age), tuberculosis

(B.C.G.), and smallpox (up to July 31, 1971). The criterion forpayment will be disablement due to vaccine damage assessedat 80% or more, according to the established rules for indus-trial injuries disablement benefit, and the receipt of attendanceor mobility allowance for conditions which could be attributedto vaccine damage will be accepted as evidence of severedamage. These payments will not prejudice the rights of those

1. Review of Clinical Genetics. A Report by the M.R.C. Subcommittee toReview Clinical Genetics, 1978.

2. See Lancet, 1978, i, 1028, 1056.