Your Health Information

 

Your health information is collected and shared between the healthcare providers looking after you.  HealthOne is a secure electronic record that allows those healthcare providers to quickly access information such as your diagnosis, allergies, encounter notes and medications.

 

This helps them to make safer, faster and better informed decisions about your care.

Your Choice

 

If your GP or Community Pharmacy is port of the HealthOne programme, some of your health information will be available to authorised medical professionals involved in your care.  If you don't want your health information shared in this way, you can "opt out" of HealthOne at any time.

 

Simply call freephone 0508 837 872 (0508 TESTSAFE) or email privacy@healthone.org.nz to confirm you want to opt out altogether, or if it is a specific information you don't want shared, ask one of your healthcare providers such as your GP to ensure that information is not shared.

Health information sharing

Your health information is shared between your healthcare providers using HealthOne, a secure system for storing electronic patient records.

 

 

HealthOne

HealthOne stores health information such as GP records, allergies, prescribed medications and test results.  Only authorised healthcare providers such as doctors, nurses and pharmacists can access that information at their place of work.

 

Sharing health information means:

  • better, safer care
  • more complete health information about you is available to your care team
  • you and your healthcare provider are able to make more informed decisions about you care
  • we are not relying on you to remember your medical history and the prescribed medicines you take
  • we waste less of your time - you only need to provide information once and because your results are in HealthOne, we don't need to repeat texts or investigations such as blood tests, x-rays or scans.

 

Your health information is only available to your care team, no one else.

 

Your health information is confidential and checks are in place to monitor who has accessed your records and why.

 

 

You can choose not to share your information

You can request that specific parts of your information are not shared, or opt off altogether so that none of it is shared by:

  • telling your healthcare provider during your visit or consultation
  • telling your pharmacist when you get your prescription filled
  • calling freephone 0508 837 872 (0508 TESTSAFE)
  • emailing privacy@healthone.org.nz

 

 

If you choose NOT to share your information:

If you opt off HealthOne, health professionals caring for you may not immediately have information they need to provide the best and safest care possible.  If you are thinking of opting off, please discuss your options with your healthcare provider or the person you speak to when you call the freephone number.

 

For more information visit www.HealthOne.org.nz or phone 0508 837 872

 

 

Contact Us

Phone : 03 372 3589

Email : info@koruskin.co.nz

 

 

HealthOne

Address

31 Colombo Street

Cashmere

Christchurch

New Zealand

Clinic Hours

Tuesday 9.30am - 5pm

Wednesday 9.30am - 5pm

Thursday 9.30am - 7pm

Friday 9.30am - 5pm

Saturday 9.30am - 2pm

Sunday & Monday closed

Cosmetic MedicineThe NZSCM is the only official recognised training and recertification body for Cosmetic Medicine in New Zealand.  You can be assured you are getting the best and safest treatment if it is from an NZSCM qualified doctor, and you can be assured the clinic is operating at “Best Practice” standards, if it has a current accreditation from the NZSCM. Koru Clinic gained its most recent NZSCM 3 year accreditation, in 2024.

** Dysport®, Botox®, Xeomin®, Profhilo®, Profhilo® Structura, Sculptra® - hover to enlarge

Botox® is a Prescription Medicine containing 100 units of botulinum toxin type A for injection. It is used for the treatment of frown lines, forehead lines and crow’s feet. It should be administered only by trained medical professionals. Talk to your specialist about the benefits/risks of the procedure in appearance medicine. Cautions: People with defective neuro-muscular transmission disorders, infection at the site of injection, glaucoma, pregnancy and lactation. Possible side effects include headaches, injection site pain/burning/stinging/bruising/swelling/redness, local muscle weakness including drooping eyelids/eyebrows, eyelid swelling, skin tightness, tingling sensations, aching/itching forehead, nausea and flu-like symptoms. If you have any side effects or concerns speak to your doctor. You will need to pay for this medicine. Normal Doctors visit fees apply. Note: Botox treatment lasts about three months and after this time further courses of treatment may be necessary. Speak to your specialist about your own situation.

Dysport® is a prescription medicine containing Clostridium botulinum Type A toxin complex for injection. It is used for the treatment of frown lines and excessive sweating. It should be administered only by trained medical professionals. Cautions: people with defective neuro-muscular transmission disorders, infection at site of injection, pregnancy and lactation. Possible side effects include headaches, pain, burning or redness at injection site, local muscle weakness including drooping eye lids, lack of feeling or nausea or compensatory sweating in other skin areas. Talk to your specialist about the benefits/risks of this procedure. A charge applies. Dysport® treatment lasts about three months and after this time further courses of treatment may be necessary.  Speak to your specialist about your own situation.

Xeomin ® is a Prescription Medicine containing 50, 100 LD50 Units of clostridium botulinum Type A toxin complex for injection. It is used for the treatment of frown lines on the forehead in adults. It should be administered only by trained medical professionals. Talk to your specialist about the benefits/risks of this procedure in appearance medicine. Xeomin treatment lasts about four months and further courses of treatment may be necessary.  Cautions: Generalised disorders of muscle activity; Infection or inflammation at the proposed injection sites, pregnancy and lactation.  Possible side effects: headache, pain, swelling or infection at injection site, local muscle weakness including drooping eye lids, lack of feeling & nausea. You will need to pay for this medicine.  Discuss with your specialist if Xeomin is right for you.

Profhilo®, containing low & high molecular weight hyaluronic acid, is a Class lll medical device for the treatment of the face and body for contours, redefinition and laxity remodelling where skin laxity is a problem. Profhilo® has risks and benefits. Do not use with treatments such as laser resurfacing or medium deep skin-peeling. Do not inject into inflamed areas or intravenously or intramuscularly. Possible side effects: pain and swelling at injection site. Individual results may vary. This medical device must be administered by a healthcare professional.
PROFHILO® STRUCTURA is a class 3 medical device and must be injected by a medical practitioner or a qualified nurse injector (operating under the supervision of a medical practitioner). PROFHILO® STRUCTURA [4.5% – 22.5 mg (H-HA) + 22.5 mg (L-HA)/1 ml Hyaluronic acid sodium salt and 4.5% – 45 mg (H-HA) + 45 mg (L-HA)/2 ml Hyaluronic acid sodium salt], injection gel in a single use sterile prefilled syringe. It is indicated for adults of both sexes for corrective / filling action of natural or induced skin depressions. PROFHILO® STRUCTURA has risks and benefits. Ask your healthcare professional if PROFHILO® STRUCTURA is right for you and to explain the possible side effects. WARNINGS & PRECAUTIONS: Do not use PROFHILO® STRUCTURA in case of known hypersensitivity or allergies to the components of the product. Do not use it in pregnant or breast-feeding women, in patients with autoimmune diseases. Do not inject intravascularly, into the muscles or tendons, or for breast enlargement. CONTRAINDICATIONS: PROFHILO® STRUCTURA must not be used in conjunction with treatments such as laser resurfacing and medium-deep peeling. Tell your doctor if any side effects concern you. ALWAYS FOLLOW THE INSTRUCTIONS YOU ARE GIVEN. Treatment costs and normal practitioner fees will apply. Please contact us for any further information or for the IFU (Instructions for use) of this product or for medical information or reporting any adverse effects.

Sculptra® (injectable poly-L-lactic acid (PLLA-SCA)) is indicated for use in people with healthy immune systems for the correction of shallow to deep nasolabial fold contour deficiencies, fine lines and wrinkles in the cheek region, and other facial wrinkles. Sculptra should not be used by people that are allergic to any ingredient of the product or have a history of keloid formation or hypertrophic scarring. Safety has not been established in patients who are pregnant, lactating, breastfeeding, or under 18 years of age. Sculptra has unique injection requirements and should only be used by a trained healthcare practitioner. Contour deficiencies should not be overcorrected because they are expected to gradually improve after treatment. Sculptra should not be injected into the blood vessels as it may cause vascular occlusion, infarction or embolic phenomena. Use at the site of skin sores, cysts, pimples, rashes, hives or infection should be postponed until healing is complete. Sculptra should not be injected into the red area (vermillion) of the lip or in the peri-orbital area. The most common side effects after initial treatment include injection site swelling, tenderness, redness, pain, bruising, bleeding, itching and lumps. Other side effects may include small lumps under the skin that are sometimes noticeable when pressing on the treated area. Larger lumps, some with delayed onset with or without inflammation or skin discoloration, have also been reported. Sculptra is available only through a licensed practitioner.

 

 

 

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