Richard H.R. White | |
---|---|
Born | |
Died | 10 December 2020 94) | (aged
Nationality | British |
Education | Emmanuel College, University of Cambridge |
Scientific career | |
Fields | Pediatrics, Nephrology |
Institutions | Great Ormond Street Hospital, Evelina London Children's Hospital, Birmingham Children's Hospital, University of Birmingham |
Richard Henry Reeve White (6 November 1926 in Newcastle-under-Lyme, 10 December 2020) was a paediatric nephrologist, [lower-alpha 1] [2] emeritus Professor of Paediatric Nephrology from the University of Birmingham [3] [4] [5] morphologist and archivist for British Association for Paediatric Nephrology. [6]
White was known for pioneering research into renal disease in children that led him to develop a renal biopsy technique that was applied percutaneously with a local anesthetic. [3] White was amongst the co-founders of the British Association for Paediatric Nephrology on 22 February 1973 and became the associations president between 1991 and 1994. [6]
White was the youngest of three children. [5] His father was Sydney White, who along with his brother ran a ladies and gentlemen's outfitters. [4] His mother was Marion White née Leigh, who was a school teacher. [4] After attending Newcastle-under-Lyme High School [5] he matriculated at Emmanuel College at the University of Cambridge in 1944 to study medicine. [7] In 1950, White graduated with a Bachelor of Medicine, Bachelor of Surgery (MB ChB). [4]
White married Patricia White née Taverner a nurse, in 1952. The couple had two boys together. [6]
White attended Guy's Hospital Medical School in London, where he completed his clinical training. [7] His early training in a number of posts, enabled him to attain membership of the Royal College of Physicians. [7] At the Royal Brompton Hospital White learned to do liver biopsy's. [8] After deciding to become a paediatrician, he trained at the Great Ormond Street Hospital (GOSH) and Guy's Hospital's in London. [7] At GOSH, he became interested in histology and particularly nephrotic syndrome in children. [4] This was known as Bright's disease [lower-alpha 2] that was first discovered by Richard Bright in 1824, but even after more than 100 years, there was very little known about it, particularly in children. [4]
In 1954, after reading an article by Robert Kark and Robert Muehrcke titled: "Biopsy of kidney in prone position" [9] White became interested in using a needle to do renal biopsy in children. [8] As a senior registrar at GOSH, he attempted to introduce a new procedure using the biopsy needle but was unsuccessful due to the opposition from the paediatricians and pathologists, who believed it could only be done under general anaesthetic. [8] However, Alan Moncrieff encouraged him to research the pathology of Liver biopsy's and managed to convince the medical staff that it could be successful. [7] After meeting Hugh de Wardener from Charing Cross Hospital who was the first to conduct Renal biopsy's in adults in the uk, [10] White immediately saw the potential in developing a percutaneous biopsy needle that could be applied with a local anesthetic [3] for children that needed a renal biopsy. [7] White compared the use of surgical biopsy techniques under a general anaesthetic against the percutaneous biopsy needle technique under a local anaesthetic in his MD thesis. [7]
In November 1959, he able to use his new technique, when he performed a needle biopsy on a child who was under general anaesthetic at GOSH. [4] This was the first time in Europe that it had been tried. [4] In 1960, White was seconded to the Makerere University College medical school in Mulago Hospital in Kampala, Uganda for two years. [11] While there, he continued working on the development of the percutaneous biopsy needle and developed a local anesthetic technique as a replacement for the general anaesthetic. [11]
When he returned in 1962, he was appointed to a position at Evelina London Children's Hospital, part of Guy's Hospital where he introduced his new biopsy technique. [4] While there, White formed a partnership with the nephrologist Stewart Cameron. [4] They both worked together to provide a comprehensive nephrology service, Cameron offering the adult service and White offering the same service for children. [4] Together they decided to conduct a clinicopathological study of children [12] with nephrotic syndrome in the region southeast and southwest of the River Thames. [3] The work started the embryo of a renal unit at Guy's Hospital that eventually led to the development of a world-class paediatric nephrology centre that was run by both Cameron and Chisholm S Ogg. [4]
White's study attracted the attention of Henry Barnett, a paediatrician who worked in the Albert Einstein College of Medicine in the New York. [13] Barnett along with Chester Edelmann and Ira Greifer created the International Study of Kidney Disease in Children in 1966 in the United States. [13] A number of international collaborators were recruited and White was the British member. [4] [13] The study on glomerular disease continued in seminal studies of children in the 1970s and 1980s. [13] White along with Renée Habib in France and Jacob Churg in the USA were the lead assessors and reported on the pathology of the biopsies. [4] The seminal study was transformational in increasing understanding of histopathology and the treatment of glomerular disease in children. [4] It also defined new techniques in the management of renal biopsy and promoted the use of clinical trials. [4]
In 1965, Douglas Hubble, who at the time was chairman of the British Paediatric Association [14] believed there was a need to develop several paediatric specialities in Birmingham and invited White to work at the Birmingham Children's Hospital [7] White was appointed to the position of senior lecturer, employed with the express purpose of developing a children's renal unit. [5] At the time the service was fragmented, meaning that patients had to visit three hospitals that resulted in the doctors having to visit the three hospitals as well. These were the Heartlands Hospital for Kidney dialysis patients at the Queen Elizabeth Hospital at the kidney transplant patients and Nephrology patients at the Children's Hospital. [15] To compound the problem, there was no paediatric nurses nor other consultants working in that speciality at the hospital at that time. [15] Seeking to create a comprehensive renal centre in Birmingham hospital in the same manner as he did in Guys, he recruited a collaborator Elizabeth Ward, who would later found the British Kidney Patient Association in 1975. [16] However, due to the level of bureaucracy at the hospital, it was a long time before the service was fully active. In 1975, White recruited Michael Hugh Winterborn as consultant paediatrician to create a dialysis service for children [17] but transplantation was only occasionally taking place by adult surgeons, not paediatric surgeons. It was only in 1997, after White retired, was the goal of a fully comprehensive renal service finally achieved in Birmingham Hospital. [6] In 1985, White became an honorary consultant. A year later in 1986 he was promoted to professor. [4] White remained at the Birmingham Children's Hospital until 1991.
In 1995, White was awarded the James Spence Medal by the British Paediatric Association for outstanding contributions to paediatric knowledge. [7]
Nephrology is a specialty for both adult internal medicine and pediatric medicine that concerns the study of the kidneys, specifically normal kidney function and kidney disease, the preservation of kidney health, and the treatment of kidney disease, from diet and medication to renal replacement therapy. The word "renal" is an adjective meaning "relating to the kidneys", and its roots are French or late Latin. Whereas according to some opinions, "renal" and "nephro" should be replaced with "kidney" in scientific writings such as "kidney medicine" or "kidney replacement therapy", other experts have advocated preserving the use of renal and nephro as appropriate including in "nephrology" and "renal replacement therapy", respectively.
Henoch–Schönlein purpura (HSP), also known as IgA vasculitis, is a disease of the skin, mucous membranes, and sometimes other organs that most commonly affects children. In the skin, the disease causes palpable purpura, often with joint pain and abdominal pain. With kidney involvement, there may be a loss of small amounts of blood and protein in the urine, but this usually goes unnoticed; in a small proportion of cases, the kidney involvement proceeds to chronic kidney disease. HSP is often preceded by an infection, such as a throat infection.
Glomerulonephritis (GN) is a term used to refer to several kidney diseases. Many of the diseases are characterised by inflammation either of the glomeruli or of the small blood vessels in the kidneys, hence the name, but not all diseases necessarily have an inflammatory component.
Membranous glomerulonephritis (MGN) is a slowly progressive disease of the kidney affecting mostly people between ages of 30 and 50 years, usually white people.
Minimal change disease is a disease affecting the kidneys which causes nephrotic syndrome. Nephrotic syndrome leads to the loss of significant amounts of protein in the urine, which causes the widespread edema and impaired kidney function commonly experienced by those affected by the disease. It is most common in children and has a peak incidence at 2 to 6 years of age. MCD is responsible for 10–25% of nephrotic syndrome cases in adults. It is also the most common cause of nephrotic syndrome of unclear cause (idiopathic) in children.
Nephritic syndrome is a syndrome comprising signs of nephritis, which is kidney disease involving inflammation. It often occurs in the glomerulus, where it is called glomerulonephritis. Glomerulonephritis is characterized by inflammation and thinning of the glomerular basement membrane and the occurrence of small pores in the podocytes of the glomerulus. These pores become large enough to permit both proteins and red blood cells to pass into the urine. By contrast, nephrotic syndrome is characterized by proteinuria and a constellation of other symptoms that specifically do not include hematuria. Nephritic syndrome, like nephrotic syndrome, may involve low level of albumin in the blood due to the protein albumin moving from the blood to the urine.
Renal osteodystrophy is currently defined as an alteration of bone morphology in patients with chronic kidney disease (CKD). It is one measure of the skeletal component of the systemic disorder of chronic kidney disease-mineral and bone disorder (CKD-MBD). The term "renal osteodystrophy" was coined in 1943, 60 years after an association was identified between bone disease and kidney failure.
Acute proliferative glomerulonephritis is a disorder of the small blood vessels of the kidney. It is a common complication of bacterial infections, typically skin infection by Streptococcus bacteria types 12, 4 and 1 (impetigo) but also after streptococcal pharyngitis, for which it is also known as postinfectious glomerulonephritis (PIGN) or poststreptococcal glomerulonephritis (PSGN). It can be a risk factor for future albuminuria. In adults, the signs and symptoms of infection may still be present at the time when the kidney problems develop, and the terms infection-related glomerulonephritis or bacterial infection-related glomerulonephritis are also used. Acute glomerulonephritis resulted in 19,000 deaths in 2013, down from 24,000 deaths in 1990 worldwide.
Mesangial proliferative glomerulonephritis (MesPGN) is a morphological pattern characterized by a numerical increase in mesangial cells and expansion of the extracellular matrix within the mesangium of the glomerulus. The increase in the number of mesangial cells can be diffuse or local and immunoglobulin and/or complement deposition can also occur. MesPGN is associated with a variety of disease processes affecting the glomerulus, though can be idiopathic. The clinical presentation of MesPGN usually consists of hematuria or nephrotic syndrome. Treatment is often consistent with the histologic pattern of and/or disease process contributing to mesangial proliferative glomerulonephritis, and usually involves some form of immunosuppressant.
Amin J. Barakat is a Lebanese-American physician known for the diagnosis Barakat syndrome.
Renal biopsy is a medical procedure in which a small piece of kidney is removed from the body for examination, usually under a microscope. Microscopic examination of the tissue can provide information needed to diagnose, monitor or treat problems of the kidney.
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Jochen H.H. Ehrich is a German pediatric doctor in the fields of nephrology and tropical medicine, professor emeritus and Former Head of the Department of Paediatric Kidney, Liver and Metabolic Diseases at the Children’s Hospital, Hannover Medical School, in Hannover, Germany.
Otto Herbert Wolff, was a German born medical scientist, paediatrician and was the Nuffield Professor of Child Health at Great Ormond Street Hospital. Wolff was notable for being one of the first paediatricians in Britain to set up a clinic for obese children. Later research into plasma lipids with Harold Salt pioneered the techniques of lipoprotein electrophoresis. He later conducted research into the role of lipid disturbance in childhood as a precursor of coronary artery disease and his recognition in 1960 of the rare condition of abetalipoproteinaemia. Wolff was also co-discoverer of the Edwards syndrome in abnormal chromosomes.
Thomas Martin Barratt was a British paediatrician and professor of paediatric nephrology. Barratt was most notable for developing a specialist service for children with kidney diseases in Britain, bringing peritoneal dialysis, haemodialysis, and later renal transplantation to ever younger children. Barratt was an early advocate for multidisciplinary care and developed a model that was later taken up by many other specialist centres across the world. His research led to a new treatments for many types of childhood kidney diseases., and for research into childhood Nephrotic syndrome and Hemolytic-uremic syndrome.
John Farrar Soothill was an English medical doctor. He began his career as a nephrologist and later became a paediatric immunologist at Great Ormond Street Hospital.
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Friedhelm Hildebrandt is the William E. Harmon Professor of Pediatrics at Harvard Medical School and Chief of the Division of Nephrology at Boston Children's Hospital. He was formerly an Investigator of the Howard Hughes Medical Institute (HHMI) and the Frederick G.L. Huetwell Professor of Pediatrics at the University of Michigan.