Peritoneal dialysis, or PD, is a home dialysis treatment that uses the lining of your own abdomen as a natural filter, rather than a machine and blood circuit. It offers flexibility and independence, and after training you or a carer do it yourself. Knowing how it works, and above all the one warning sign to act on quickly, makes PD much less daunting. This guide explains what to expect, with the key safety point front and centre.
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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 training. The most important thing to know: cloudy drained PD fluid, with or without tummy pain or fever, can mean peritonitis, an infection of the abdominal lining. Contact your PD unit immediately, and keep the cloudy bag to show them. Keep clean technique at every exchange.
How PD works
In peritoneal dialysis, the lining of your abdomen, called the peritoneum, does the filtering. It is a natural membrane richly supplied with tiny blood vessels. Dialysis fluid is run into the abdominal cavity through a soft tube, where it draws waste products and excess fluid out of the blood across the peritoneum, and is then drained away. Because the filtering happens inside your body, there is no external blood circuit and no needles into a fistula for each treatment. This is one reason some people prefer it, and it can make PD gentler on the heart and blood pressure than centre haemodialysis for certain people.
The catheter and exit site
PD is done through a soft, flexible tube called a PD catheter, placed by a small operation into the abdomen, usually near the navel, with one end coming out through the skin at a point called the exit site. The catheter usually needs a few weeks to heal and settle before regular use. Looking after the exit site, keeping it clean and watching for early signs of infection, is a daily part of PD, taught by your PD nurse.
The exchange
The basic cycle of PD is called an exchange, and it has three steps: fluid is run in (fill), left to sit in the abdomen for a set time (dwell), and then drained out (drain), carrying the waste and excess fluid with it. The fluid contains glucose, which draws off excess water, and your team advises which strength of fluid to use depending on how much fluid you need to remove. You do several exchanges over a day or overnight.
CAPD and APD
There are two main ways to do PD. CAPD (continuous ambulatory peritoneal dialysis) uses manual exchanges done by hand, typically several times a day, each taking a short while, with fluid dwelling in between; it needs no machine or electricity. APD (automated peritoneal dialysis) uses a machine, sometimes called a cycler, to do the exchanges automatically overnight while you sleep, freeing up your day. Your team helps you choose the option that fits your life, and some people switch between them at different stages of their treatment.
A home therapy and clean technique
PD is a home therapy that you or a trained carer carry out after a training course from the PD unit, which is why it offers independence and can fit around work, study and family. The single most important habit is clean, careful technique at every exchange and every time you handle the exit site: washing your hands, using a clean space, wearing a mask if instructed, and handling the connections carefully. This is your main defence against introducing infection.
Peritonitis, the key sign
The one complication every PD patient must know is peritonitis, an infection of the peritoneum. The classic sign is cloudy drained fluid, usually with tummy pain, and sometimes fever, nausea or feeling generally unwell. A single cloudy bag is enough to act on. Peritonitis is treatable, often with antibiotics added into the PD fluid, but it needs prompt attention, so contact your PD unit immediately, do not wait to see whether it clears, and keep the cloudy bag to show them. Repeated episodes can damage the membrane over time, so catching each episode early and treating it promptly is what protects your ability to keep using PD.
Daily life and getting help
Day to day, PD becomes a routine of exchanges, exit-site care, checking your weight and fluid balance, and keeping your supplies stocked. Report an exit-site infection (redness, tenderness, swelling, crusting or discharge, especially with fever) to your unit promptly, as it can lead to peritonitis if untreated, and report drainage problems or feeling unwell. In Singapore, your hospital PD team is your first contact, and 995 is for emergencies such as severe pain, collapse or being seriously unwell. Over time, most people find that peritoneal dialysis fits into their normal daily life far more easily and naturally than they had first expected when they started out.
Related dialysis topics
- Living with dialysis
- Haemodialysis: 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
- Kidney Care UK – Peritoneal dialysis: kidneycareuk.org
- NIDDK (NIH) – Peritoneal dialysis: niddk.nih.gov
- NHS – Peritonitis: nhs.uk
