Haemodialysis is the most familiar form of dialysis: your blood is filtered through a machine and returned to you, usually at a dialysis centre several times a week. Knowing how it works and what a session is like takes much of the worry out of starting. This guide walks through the process, what to expect during and after a session, and the small number of warning signs worth knowing.
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In a medical emergency, or for severe or sudden symptoms such as breathing difficulty, chest pain, fainting or stroke signs, call 995 immediately.
This is general information and does not replace your renal team’s advice. Tell the unit staff at once if you feel dizzy, sick or crampy during a session. Never miss or shorten a session without contacting your unit. Apply firm pressure to any bleeding from your access, and call 995 if it will not stop.
How haemodialysis works
In haemodialysis, blood is drawn from your body through a needle or a catheter, pumped through a machine and a filter called a dialyser, where waste products and excess fluid are removed, and then returned to you. The dialyser acts as an artificial kidney, and the machine controls how fast the blood flows and how much fluid is taken off. Your blood is being cleaned continuously throughout the session, a little at a time, before being returned. Only a small amount of your blood is outside the body at any moment, which is one reason the treatment is safe when carefully monitored.
In-centre sessions
Most people have haemodialysis at a dialysis centre, which may be in a hospital or a community satellite unit. As the NHS describes, it is commonly done about three times a week, with each session usually lasting a few hours, though the exact frequency and length are set by your renal team based on your size, any remaining kidney function, your fluid gain and your blood results. Some people are later trained to do haemodialysis at home, covered in our home haemodialysis guide.
What a session is like
A session follows a routine that quickly becomes familiar. You are usually weighed before and after, so the team can check how much fluid was removed and work towards your target, or “dry”, weight. Your blood pressure and the machine are monitored throughout. Once you are connected, the time is yours: many people read, rest, watch something, use a phone or tablet, chat, or sleep. The staff are there throughout to keep an eye on you and the machine. Many people get to know the staff and other patients at their unit well, and the regular routine becomes a familiar part of the week.
The access you need
Before haemodialysis can start, you need a way for blood to be taken and returned, called your access. This is usually an arteriovenous (AV) fistula in the arm, sometimes a graft, or a tunnelled catheter (line) when a fistula is not ready or possible. A fistula needs to be created ahead of time and takes weeks to months to mature before it can be used. Looking after your access is one of the most important parts of dialysis life, covered in our access care guide.
Common during-session effects
Some effects during a session are common and are managed by the unit on the spot. The most frequent are a drop in blood pressure, which can make you feel dizzy, sick or faint, and muscle cramps, both often related to fluid being removed. Tell the staff at once if you feel unwell, so they can act, for example by slowing the fluid removal or adjusting the machine. These are routine issues the team handles during dialysis, not something to manage alone.
Fluid between sessions
Because failing kidneys make little or no urine, fluid builds up in your body between sessions. Too large a fluid gain means more has to be removed in one session, which is harder on the body and more likely to cause cramps and low blood pressure. This is why keeping to the fluid, and often diet, limits agreed with your team matters so much, and it is covered in our fluid and diet guide. Steady, moderate fluid gains make each session smoother.
After a session, and red flags
It is common to feel washed out or tired for a while after dialysis, and many people plan a rest around their dialysis days. Contact your unit for bleeding from your access that will not stop with firm pressure (call 995 if it is heavy or will not stop), for a hot, red, swollen or painful access, or if you lose the usual buzz over a fistula. Also seek help for severe breathlessness or chest pain, which can signal too much fluid. Keeping this simple split clear in your mind, and sharing it with your family, means you can act quickly and correctly in a worrying moment. In Singapore, keep your unit’s number to hand, and 995 is the emergency number.
Related dialysis topics
- Living with dialysis
- Peritoneal dialysis: what to expect
- Home haemodialysis
- Access: fistula & catheter care
- Fluid & diet on dialysis
- Managing problems & when to get help
- Staying well & active
- Travelling & holidays
- Emotional wellbeing & daily life
- Kidney specialists in Singapore
Sources
- NHS – Dialysis: nhs.uk
- NHS – Dialysis, how it is done: nhs.uk
- Kidney Care UK – Haemodialysis: kidneycareuk.org
- National Kidney Foundation – Hemodialysis: kidney.org
