Seeing Dr. Moore's historical note reminded me of the years when I worked as a medical laboratory technologist (aka clinical lab scientist) for Canada's national blood supplier, the Canadian Red Cross Blood Transfusion Service (now Canadian Blood Services) in Winnipeg. The facility was (and is) a combination blood center and transfusion service that performs all crossmatching for the city and small rural hospitals in the province, along the lines of Puget Sound Blood Center in Seattle. It was the mid-60s to late '70s, a time when we performed risky practices and never gave safety a thought.
Back then I knew of Dr. Moore, whom everyone called "Paddy" Moore. To my young eyes (I was practically a child laborer!) he was a "biggie" at National, meaning national headquarters from whence all wisdom seemed to flow.
Those golden days were pre-AIDS. See
Talk about a primitive test - you had to pipette just the right amount of liquid agar on a glass plate (an art in itself), wait for it to set, punch out wells, add reagents, incubate, then look for precipitin lines (positives) by holding the glass plate against a black background. I often had difficulty seeing even the positive control!
As an aside, it was an early indiction that my future lay more on the transfusion service side than on the blood centre side. The latter I eventually came to refer to as the "dark side" just to tease my blood centre buddies who worked increasingly with automated instruments. To me they were becoming less and less true blood bankers compared to those who worked in transfusion services and got "down and dirty" with their hands. Eventually, of course, automation made inroads into pretransfusion testing, so we are all now disciples of the dark side.
Back to HbsAg testing by CIEP: Once a colleague came running to me exclaiming, "Pat, help! I just swallowed the positive hep B control!" Frustrated with trying to control the tiny bulb on a tiny pipette (actually just a capillary tube), she had used her mouth to suck up the reagent and dispense it! We called National and their sage advice was to "drink lots and lots of water" and let nature take its course. Of course, the positive control was presumably not infectious as it was only the surface antigen, but who knows what all was in the darn reagent.
Those were also the bad old days in more ways than one. For example, we used no SOPs, if you can imagine. All instructions were passed from trainer to new employee. Talk about standardization - NOT!
Near the end of my time at the Winnipeg BTS (by now I was a senior technologist and trainer) one year I decided on my own to write a procedural and policy manual for the crossmatch laboratory on my holidays. I went to a cottage on a nearby lake for two weeks and in between canoe trips wrote the manual in long-hand (pre-computers days too). All on a volunteer basis without official sanction, and, of course, they used the manual.
Having recently gotten married, my husband thought I was nuts. But he soon grew to understood that the organization was family and that working for the BTS was getting paid to do something that my colleagues and I loved and was great fun to boot.
One of my fondest memories from my Red Cross days was how we used to "shuck" (pour out) blood clots from 100s of donor specimens into kidney dishes before preparing 5% saline suspensions for red cell testing. All the while smoking and drinking coffee, of course. Time was a factor and those clots got tossed with wild abandon - it was the start of what could be a very long day depending on the clinic size. We worked until all blood was tested and sorted (put into inventory), no matter how long that took. For the 1000+ donor clinics held on the day after New Year's Day that could be from 07:00 to 23:00 hrs. No union to influence working hours in those days, either.
But I digress. To start each day we would shuck like crazy until the kidney dishes were full. Blood would splatter everywhere, including all over us, our smokes and coffee cups. No gloves, of course, only white lab coats that we wore everywhere including into the lunch room. My most vivid memory from those days is the taste of blood on my cigarette filter (I gave up the cancer-emphysema sticks in 1987). The blood tasted awful, probably more so as I'm a vegetarian.
The second most vivid memory is of bloody finger streaks on the back of everyone's lab coat (after all, techs need to keep their hands clean and buttocks are as good a place to wipe as any). Some of us were regular Picassos!
When hepatitis B testing was instituted at the blood centre (during my years there we went through counterimmunoelectropheresis, reverse passive hemagglutination, and radioimmune diffusion, all now considered prehistoric), one year all lab staff were tested for both HBsAg and anti-HBs. Of the 20 or so technologists none were positive for HBsAg and only one was anti-HBs positive.
Of course, the BTS was testing healthy blood donors for hepatitis and Canada had a relatively low prevalence rate. Mind you, some of the specimens did test positive, and perhaps some of those made their way to my cigarette filters. Also, in the 1960s we bled donors from Manitoba's two penitentiaries. Indeed, once the rate of HBsAg in jails became known, prisoners were dropped as donor sources.
In retrospect, based on my experience working at the Red Cross BTS in the pre-AIDS days, I view the risk of contracting hepatitis and other blood-borne agents from lab-related activities as being low but certainly not zero. Consider that there were two technologists in the neigbouring province of Saskatchewan who contracted hepatitis B and died from mouth pipetting positive controls in the chemistry lab. We in the blood centres had luck on our side.Baruch Blumberg , awarded a Nobel Prize in 1976 for his discovery of HBsAg, tells the story of how his laboratory technologist came down with hepatitis B before they knew what the Australian antigen was.
Even given that the risk of contracting a blood-borne disease in a blood centre laboratory is low, personally, I would not want to play Russian roulette with a million-bullet gun cartridge containing only one bullet. Sooner or later, someone gets the bullet. The low risk may apply to all the risks that we try to prevent by using universal precautions, especially if the causative organism (unlike HBV) does not survive well on inanimate surfaces such as counter tops.
Today's students and younger lab professionals are astounded at the practices of smoking, mouth pipetting, etc., in the laboratory. In retrospect, even this vegetarian, once blood eater, finds them surreal.
It's hard to realize that when I first joined Canada's national blood transfusion service it was less than 20 years old. A Yikes! thought but somehow it puts everything in perspective.
Cheers, Pat
Pat's reminiscing about the good old days at Red Cross, got my Red Cross memory banks going about Hamilton Centre in the early 1980s.
ReplyDelete* Smoking was permitted EVERYWHERE except for the lab: lunch room, offices, meeting rooms, hallways, transport office, etc.
* We wore our lab coats EVERYWHERE: washrooms, offices, lunch room--hey, people had to carry their cigarettes in something! :>)
* We had a clean area in the lab by the hand washing sink where cups and glasses were stored. We (if you wanted to) could drink in this 'clean area'
* Getting teased by a senior staff member for refusing to pipette the working solution of papain by mouth. Later I found out that more than one person used that pipette--by mouth too! (Eeewww!)
* Why waste your money on purchasing bone and blood meal for your roses when you can get it for free? Red cells that were discarded for malarial deferrals were taken home by some staff members and used to fertilize their prize roses.
* Labelling 600+ tubes from the clinics from the day before for the HBsAg RIA test
* Not lining up the trays containing your completed RIA glass beads with the transfer boxes containing the tubes, and ending up with what seemed to be a million little beads all over the floor. That tray also happened to contain your controls. That testing that took you 4++ hours to complete, now has to be repeated.....
* When the methodology switched to ELISA, the bead/transfer to tube system remained, so guess what? We still ended up with beads on the floor. We were so thankful when microtitre plates hit the scene for Transmissible Disease (TD) testing--no beads--YIPPEE!
* 'National office' was located in Toronto (later moved to Ottawa) and seemed God-like. When the TD or Virology lab from National called and asked for YOU specifically, you knew you were in trouble!
* Our Tuesday morning educational meetings where we heard some great speakers or the front line MLTs took turns presenting journal articles. If we were presenting, each us said a silent prayer that the questions that Dr. Blajchman would pose to us would not be too difficult. <8-)
* Being educated and mentored by some of the greats: Sheila Ferguson, Joan Marshall, Dr. Morris Blajchman (I still work with him), Dr. John Kelton, and Nancy Heddle would sometimes visit and teach us.
* Using the 16-C Autogrouper and the old BG-15 as a back up
* Using autoanalyzers for antibody screens well past their expected life times. We could no longer get spare parts, so they were held together with spit and a prayer
* RNs on the clinics always wore white uniforms, white duty shoes and caps. Clinic assistants always wore powder blue uniforms--polyester of course!
* People getting stuck in the walk-in freezer! BBRRR....
* Working on exciting antibody cases referred into us from our hospitals. Finding those 2/1000 compatible units
* Watching new staff freeze test cells in liquid nitrogen for the first time via the syringe method. They always decorated the ceiling with the cells until they figured out how much pressure to apply to the syringe
* The excitement surrounding the implementation of the first computer system at Red Cross: BLIS--Blood Information System
* Getting called back four times in one night to issue blood to one of our 28 hospitals and going to work the next day with no sleep
* We were small enough that everyone working at the Centre knew everyone. We celebrating and mourned together
* Finally, when I was the 'baby' of the lab--the youngest technologist. A distinction I held for about 4 years. I never have to worry about earning that distinction now!
Denise Evanovitch