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Laboratory book

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Mission statement of the paediatric laboratory

  • We deliver exact and reproducible results thanks to our precise working methods, which are carried out under standardised conditions.
  • We endeavour to deliver results as quickly as possible in order to support the patient's treatment.
  • We ensure our quality through continuous training of the laboratory team.
  • Thanks to continuous training and further education, our knowledge is constantly being expanded.
  • Our analysis procedures are continuously monitored through regular internal and external quality controls.
  • We ensure our quality through an elaborate quality management system.
  • We are committed to sustainability, i.e. a balance between social solidarity, economic efficiency and ecological responsibility.
  • Patients' lives are our greatest asset, and this is at the centre of our work.
  • We offer services around the clock.
  • We constantly strive for improvements and achieve results through constructive dialogue.

Performance mandate

The paediatric laboratory of the UKBB primarily provides services in the field of haematology. This is done for all UKBB outpatients and inpatients, including neonatology in the USB Women's Clinic.

The services of the analyses offered in the paediatric laboratory can also be used by external clients.

If you have any questions regarding order requests, pre-analysis and interpretation of analysis results, we will be happy to advise and support you by telephone. Regular internal and external quality controls are carried out on all parameters analysed by us in order to guarantee the accuracy of the results.

Laboratory services that are not offered by the paediatric laboratory are carried out in collaboration with external laboratories, such as the USB central laboratory.

We are also involved in various studies.

Since September 2017, we have been internationally accredited by the Swiss Accreditation Service (SAS) in accordance with ISO 15189 and regularly review our compliance with this standard.

Laboratory parameters offered that are not or not yet accredited are specially labelled by us.

Data security and data protection

Our patient information and analysis results are stored in accordance with legal requirements. In addition, backup copies are made on a regular basis. Our results are transmitted electronically for internal clients and by fax and letter or HIN e-mail for external clients.

See also Data protection of the UKBB

We would like to point out that all laboratory results are subject to data protection. Findings may only be viewed by authorised persons.

Copying and passing on to unauthorised persons is not permitted.

Quality management

The well-being of patients is at the centre of our work. We are aware that we provide the treating physicians with results that can lead to the detection and/or treatment of diseases. For this reason, and in order to fulfil the high demands of our clients, we work in accordance with the requirements of ISO 15189.
We are constantly endeavouring to meet these requirements:

  • The optimisation of work processes
  • Clear and regulated work processes
  • A clear laboratory organisation and structure
  • A high level of transparency
  • Increased performance
  • Traceability and traceability of the measurement results
  • A sustainable awareness of quality
  • Error reductions
  • Cost reductions

The QM system is subject to continuous review to ensure its suitability for all users. The requirements and regulations to which the paediatric laboratory has committed itself, as well as their implementation and continuous improvement of the laboratory's internal QM system, are mandatory and are described in the QM manual.
We always endeavour to offer the highest possible quality that corresponds to the current state of technical knowledge.

Sample material

Before the patient samples are processed, they are checked for the following points:

  • Completeness of the material
  • Quality of the material (e.g. clots, too little material, insufficient filling volume, etc.)
  • Conformity of the sample tube label with the sample (e.g. EDTA, citrate)
  • Conformity of the sample label (surname and first name) with the electronic order

If incompleteness or errors are detected that lead to incorrect analysis results, the order is not processed. However, incorrect orders remain and are commented on accordingly. The client will be informed immediately.

Results of the laboratory analyses

The results of our laboratory analyses are subjected to technical and medical approval before they appear in the report. The technical approval always includes a check of the accuracy of the analysis, e.g. on the basis of the accompanying controls, the correct functioning of the equipment, the stability of the reagents, etc. It ensures that there are no doubts on the technical side. It ensures that there are no doubts about the result from the technical side. This always takes into account the pre-analysis.
During medical validation, the plausibility of the results is checked and interpreted on the basis of influencing variables, available clinical data and preliminary values.
Technical and medical approval is given by a BMA.
If further clarification is required or if there are any uncertainties, the client will be contacted by telephone.
Reports are generated electronically and automatically.

Internal and external quality controls

Internal and external quality controls are carried out on the basis of Qualab regulations.
Quality controls are used to ensure the precision, accuracy and reliability of the analysis results.
Internal quality controls are carried out several times a day or for each batch.
With POCT systems, internal control measurements are carried out at least every 2 weeks.
One or more control samples with different known concentrations are analysed. The result is compared with the target value and must be within the permitted tolerance range. Internal quality control can thus detect analytical problems that are attributable to the reagents or a device, so that measures can be initiated as quickly as possible to achieve the specified values.
Participation in external quality controls (round robin tests) takes place 4 times a year, depending on the analysis. For this purpose, a control provided by an external control centre and determined using the same analytical system is analysed.
The measured values are sent to the control centre and compared with the results of other participating laboratories. A statistical evaluation is carried out. The paediatric laboratory receives a report of this statistical evaluation, which lists and assesses the quality of the measured analyte. External quality control is used for targeted quality monitoring and for the subsequent detection of deviations or errors. If necessary, corrective measures are initiated.

Complaints and error handling

Despite extensive quality assurance and endeavours on our part to ensure the quality of our services, errors may occasionally occur. We therefore ask all clients to inform us immediately in the event of any findings that appear implausible.
Every reported abnormality or complaint, whether noticed internally or reported by the client, is documented and processed in the paediatric laboratory.
The aim is to ensure the requirements and satisfaction of our clients, but also to further develop our own quality system.
We have a documented procedure for handling complaints and errors. This procedure can be viewed on request.

Laboratory orders and sample acceptance

In principle, only parameters listed in our analysis directory can be analysed.

The needs and requirements of our clients are at the centre of our work.

You can therefore inform us of your wishes and requirements for the introduction of new analyses at any time. Following a cost-benefit analysis, the laboratory management will discuss the feasibility of the project with the management.

The emergency programme shows the analyses that we offer outside of normal operation.

We endeavour to process all laboratory orders as quickly as possible. You will receive the results of general routine parameters within 2 hours, microscopic differentiations within 1 day, depending on the workload.

If it is an emergency order, please select the priority "Emergency" in i/med. The order will then be processed within 1 hour from Monday to Sunday, microscopic differentiations within 90 minutes (from Monday to Friday), unless the questions are complex.

Please note that our devices are serviced between 07:00 and 08:00, so there may be slight delays in order processing during this period.

Please also note that we can only fulfil laboratory orders (including capillary blood samples taken by the laboratory) once a definitive order request has been received. The order is entered by the client.

Orders outside of normal operation

We would like to draw your attention to the fact that the paediatric laboratory is only available on call after 9.00 pm. In general, you should only send orders outside normal working hours if they really are emergency orders. Microscopic differentiations of blood counts and cerebrospinal fluid preparations that are to be carried out in emergency mode must also be notified by telephone by the responsible senior physician. In other cases, microscopic differentiations will not be carried out until the following day. An order outside of regular working hours is subject to a surcharge of 50 tax points.

Unfortunately, due to the relatively short sample stability, it is not possible for us to store samples for you until the next working day in order to process them routinely. (Exception: stool for OBTI test).

The i/med system from Dorner is used for electronic order entry by the paediatric laboratory (UKBB) and the University Hospital Basel (USB).

If you have problems with the information system or barcode printer, please contact the service desk team with Cc at Beatrice Jauslin and Vera Fanaj.

For a detailed description of order entry, see also Quick guide i/med (LIS).

You can find the training documents from the introduction day here: Training i/med.

If analyses are missing or if you wish to record new analyses in i/med, the following process is used:

Process Missing analyses in i/med
Please fill in the Form Missing analyses in i/med and send this via E-mail to the service desk.

The paediatric laboratory can only accept laboratory orders (including capillary blood samples) if a completed paediatric laboratory order form has been submitted.

The right order forms

The currently valid version of the order form can be found on our website www.ukbb.ch, in the closed area for referrers.

Please always use the latest version of the order form and do not make too many copies, as we are constantly updating the forms.

Please use the order form for analyses of chemistry, hormones, narcotic or metabolic prescriptions or parameters that are not carried out by the paediatric laboratory No.11 Paediatrics of the USB. This order form will be sent to you by the USB. If no more order forms are available, you can reorder them from the USB by fax (fax +41 61 265 46 00).

Shipping
If there is an order for the paediatric laboratory at UKBB, the USB order form no. 11 is also sent to the paediatric laboratory at UKBB. If there is only an order for the USB, order form no. 11 is sent directly to the USB.

Outpatient admission
If you refer patients directly to UKBB for a blood sample, they will be admitted via the Outpatient Department on the ground floor on arrival at UKBB.

Patient samples are considered potentially infectious and therefore dangerous goods. They must be transported in accordance with special regulations to protect people and the environment. Leakage of the sample should be prevented at all costs.

It is therefore essential to use special liquid-tight transport bags to protect the samples.

Samples are sent directly by the requesting department via pneumatic tube (or STA in the event of a pneumatic tube failure). Detailed instructions for the pneumatic tube system and STA can be found on the intranet.

The desired destination address is entered for the pneumatic tube system (five-digit number). A list of all numbers can be found next to the pneumatic tube systems. It is important that the sample material taken is forwarded to the appropriate laboratory immediately, regardless of the type, as the sample stabilities are different and can significantly influence the analysis results.

Sample dispatch for external senders

The paediatric laboratory offers all external senders free collection of sample material by courier. The Metropol courier service is available for this purpose and can be called out from 07.00 to 19.00.

We ask you to use the padded packaging material provided by us.

Please note that contaminated, leaked or broken sample material will not be accepted for safety reasons.

In such cases, the client will be informed by telephone.

The sample material will be returned if necessary.

Before the analyses are carried out, the incoming sample material is checked for defined criteria (clots, insufficient filling volume, etc.). If incompleteness or errors are detected during this check, we will inform you by telephone.

Repeat orders are possible at any time, provided the sample quantity is sufficient and the stability period of the sample can be maintained.

The stabilities can be found under the respective analyses. Notify the laboratory in advance of the repeat order so that the remaining sample quantity and sample stability can be checked.

  • ​​​​Repeat orders for the paediatric laboratory are requested electronically in i/med.
  • To do this, select the "Reorder" button in i/med.
  • Enter the order number of the original findings in the "Comment" pop-up window.
  • Select the corresponding analysis(es) and save the order.
  • Select the label printer Laboratory and print the labels, then reset the printer.

A new order is generated, which is visible as a repeat order.

The executing BMA checks the possibility of realising the order extension according to laboratory medical criteria. The existing order is then extended or a new order is created. Repeat orders that require a new order are labelled as "repeat order".

If the repeat order cannot be realised, we will inform you by telephone.

Preanalytics

Pre-analysis refers to all processes prior to the actual laboratory analysis, from the preparation for obtaining the sample, the actual sample collection from the patient, sample transport and processing in the laboratory.

Pre-analytical errors are the most common cause of implausible test results. As most pre-analytical procedures are beyond the control of the laboratory, this aspect can only be addressed in close co-operation between the laboratory and the senders.

If special attention is paid to pre-analysis, errors can be reduced and unnecessary costs due to control tests can be avoided. For this reason, we attach great importance to the information on pre-analysis in this laboratory book.

Paediatric laboratory (UKBB):
The sample quantity can be taken from the info box next to the sample material during electronic order entry in i/med.
This specified sample quantity corresponds to the minimum quantity, unless the addition: "precise" appears in square brackets. In this case, the sample quantity must correspond exactly to the tube volume.

USB:
Attention! Sample quantities are not stored for some analyses. There is a risk that the total volume of the respective material is displayed too low.
For sample quantities concerning the USB, please contact the respective department.

The aim of each examination is to obtain a sample that is representative of the patient's condition, suitable for the requested examination and only minimally altered by influences (sample collection, sample transport, etc.).

There are basically two types of test material that can be used for routine examinations: venous blood and capillary blood, which can be obtained from the finger or heel.

The blood composition in the various vascular areas is very different. About 65 % of the total blood volume is in the veins, only 20 % in the capillaries, the remaining 15 % fill the arterial legs.

Capacity changes in the venous and capillary system have a considerable effect on the distribution and composition of the blood. In the capillary system, the proportion of plasma increases with decreasing vessel width to the detriment of the cellular components and high-molecular substances, as plasma water and low-molecular substances increasingly flow into the pericapillary space. While the composition of the blood is largely constant in the arterial and venous vascular areas, metabolic and substance exchange processes take place in the capillary area, which can lead to very rapid changes over time.

On the other hand, in the typical stress or shock situation, the opposite phenomenon occurs: the capillary periphery is poorly perfused and does not provide representative results for the entire circulation. These physiological conditions clearly qualify venous blood sampling over capillary sampling.

When can capillary blood collection be used?
Capillary blood collection is the preferred method of sample collection for newborns and infants when very little blood is required. Under certain circumstances, capillary blood collection may also be the method of choice for older children, for example in the case of

  • Patients with burns or scars at blood collection points for venous blood
  • Patients with difficult venous conditions that make venous blood sampling impossible
  • Patients who have IV access in both arms or hands
  • Obese patients
  • Patients who require regular blood samples to be taken at short intervals
  • Patients whose veins are intended for intravenous administration or chemotherapy
  • Patients for whom only one test needs to be performed, for which only a few drops of blood are sufficient (POCT analyses)

In order to achieve comparable values, the conditions for blood collection should be as constant as possible.

As a rule, the blood sample is taken in the morning between 7 and 9 a.m. on the sober patients (12-hour fasting period). In exceptional cases, it is possible to deviate from these guidelines (e.g. admission of acute patients, checks following the administration of medication, etc.).

Outpatients should rest for at least 15 minutes before a blood sample is taken. Inform the patient or, if applicable, the legal guardian about the measure and its purpose. The time of collection must be selected when the order is entered in i/med.

Please also enter influencing variables such as anticoagulation for the interpretation of the coagulation and the medication (e.g. Neupogen) for the interpretation of the blood count in the i/med.

The UKBB uses monovettes and microvettes from Sarstedt.

The respective tubes have colour coding:

  • Serum: Red
  • Citrate: Light blue
  • Lithium heparin: Green
  • EDTA blood: violet
  • Buffered citrate: turquoise

When an order is requested in i/med, the test material to be used is indicated on the label. Please always ensure that the appropriate sample material is labelled with the correct label.

NEVER fill a tube with the contents of another tube!

NEVER use a capillary with any other additive!

Monovettes for venous blood collection

Microvettes for capillary blood collection

Vessels for other samples

Only monovettes that are used for analyses in the paediatric laboratory are listed. This also applies to information and instructions for sample collection.

For information on examinations that take place at the USB, please use the USB laboratory book, which is listed on the intranet under Quick Access.

We ask for your understanding in this regard. Changes made by the central laboratory to its analyses are not subject to our control.

The order of the blood collection tubes (venous)

1. heavy metal monovette with heavy metal-free needle (rare!)

2. blood culture (caution, avoid contamination!)

3. serum (red and beige), if without Coagulation activator

4. citrate (light blue)

5. serum (red and beige), if with Coagulation activator

6. lithium heparin (green)

7. EDTA (purple)

8. blood sedimentation (grey)

9. other (e.g. sodium fluoride, light grey)

If not all sample tubes are required, proceed in the same order as described above, omitting the sample tubes that are not required.

However, the citrate vial should not be used as the first sample vial, as this can falsify the coagulation tests. In this case, the first blood should be discarded before filling the citrate vessel to be on the safe side.

The order of the blood collection tubes (capillary)

1st BGA capillary

2. coagulation (light blue)

3. EDTA 200 µl (violet)

4. erythrocyte sedimentation rate (violet)

5. sodium fluoride (grey)

6. EDTA 500 µl (violet)

7. lithium heparin (green)

8. serum (red)

The sequence of capillary blood collection differs from venous blood collection, as clotting can occur more quickly here.

It is generally recommended that capillary blood collection is only carried out if little material is required. See also chapter: "Selecting the type of blood collection"

If not all sample tubes are required, proceed in the above order, omitting the sample tubes that are not required.

Citrate additive:

Citrate prevents the blood sample from clotting. The blood cells are centrifuged in the laboratory and the coagulation tests are analysed in citrate plasma, while the sedimentation reaction is carried out on citrate whole blood.

EDTA additive:

EDTA prevents the coagulation of the blood sample and the biological oxidation of sensitive components. EDTA blood is mainly used for haematological tests.

Heparin additive:

Heparin prevents the blood sample from clotting. Osmotic resistance is performed from heparinised whole blood.

Tubes containing additives must be mixed immediately after blood collection (do not shake).

Venous

  • Please check the identity of the patients
  • Patients should sit or lie down, if necessary patients should rest for 15 minutes before you start taking blood samples
  • Wear gloves
  • Disinfect the skin with a suitable disinfectant
  • Do not stow the arm for too long (haemolysis)
  • The patient can make a fist during the puncture, after which the hand should be opened again (no pumping)
  • Observe the order of the tubes
  • Each tube must be carefully mixed after removal (do not shake)
  • Dispose of the used cannula in a disposal container (according to the disposal concept)
  • Label the tubes and ensure that the correct name is on all tubes; the labels must be attached in such a way that the contents can be seen and the fill level checked

Capillary
Please remember that the cell concentrations measured in capillary blood are not very representative of the total circulation. As a general rule, venous blood is more suitable than capillary blood. In direct comparison, a selective enrichment of leukocytes in the capillary area can be detected. Clinically significant differences - capillary blood > venous blood - of 1-4 leucocytes/µ are very common. Under these conditions, a slight leucopenia can be overlooked or a value in the upper normal range can be misinterpreted as a leucocytosis.

Important points when performing capillary blood sampling

  • Wipe the puncture site with disinfectant (and allow to dry - the puncture site must be dry)
  • Place the lancing device on one side (ideally the 3rd or 4th finger), apply slight pressure and press. The needle/lancet is automatically released when sufficient pressure is applied
  • Wipe away the first drop of blood
  • Compress fingers on the middle phalanx from above and below (not at the level of the puncture site or on the side)
  • Important: The blood should flow without strong squeezing
  • If the blood stagnates, wipe over the puncture site with the swab
  • After blood has been taken, haemostasis is achieved by pressing on a swab
  • Then close the lid (including the microvettes without capillaries) and mix carefully by tilting several times
  • Label tubes with patient barcodes, please ensure the correct names are on all tubes, the labels must be attached in such a way that the contents can be seen and the fill level checked

Newborns and infants

  • Capillary blood samples are taken from the heel of newborns and infants in the first few weeks of life (up to 3 months, pay attention to the size of the heel and use your finger if necessary)
  • If necessary, the administration of Algopedol Sucrose 24% (for children <8 months)
  • Two minutes Before the procedure, slowly instil Algopedol Sucrose 24% with a syringe from the corner of the mouth, use a pacifier if necessary, 2 ml may be administered from a body weight of 3 kg.
  • The puncture is performed with a light green Quickheel Lancet, on the lateral heel edge near the sole of the foot

If necessary, the laboratory can be called to take blood samples in special exceptional cases; the following process applies:

Capillary blood collection at UKBB

Bone marrow punctures and special blood samples, e.g. for pyruvate analyses and ketone body analyses, must be registered in advance and as early as possible by telephone.

Bone marrow
For a bone marrow puncture, it is necessary to register by telephone with the paediatric laboratory, if possible the day before at the latest.

The following information should be provided if possible:

  • Name of the patient
  • Location of the bone marrow puncture
  • Approximate time of bone marrow aspiration
  • Diagnosis/questioning (so that sufficient smears can be prepared for special staining and external dispatch)
  • Information on additional colouring required

Additional analyses and required material

  • The differential blood count and the reticulocyte count must be performed on the same day
  • The order must be created before the bone marrow puncture

Dab preparations
The paediatric laboratory must be informed in good time by telephone if swab preparations are to be made. The BMA produces the swab preparations.

The following information should be provided if possible:

  • Name of the patient
  • Place of manufacture
  • Diagnosis/questioning (so that sufficient preparations can be made for special staining)

Swab preparations
Swabs are taken from pustule contents or other skin rashes. The paediatric laboratory must be informed by telephone for the preparation of swab specimens.

The attending physician prepares the swab specimens, the BMA is present. The diagnosis or question should be communicated to the paediatric laboratory if possible.

Pyruvate
For the pyruvate analysis, a telephone appointment with the paediatric laboratory is necessary. The laboratory must be present when the venous blood sample is taken.

The doctor or nursing staff will unstowed Approx. 1 mL of blood is taken in a native syringe (without additives). The collected material is handed over to the BMA present, which immediately pipettes the blood in a ratio of 1:2 into ice-cold 8% perchloric acid.

Further processing and sample dispatch takes place in the paediatric laboratory.

Keto body
For the keto body analysis, it is necessary to register by telephone with the paediatric laboratory. A biomedical analyst must be present during the venous blood collection. The doctor or nurse draws approx. 1 mL of native blood (without additives) in a syringe. The collected material is handed over to the biomedical analyst, who analyses the blood sample.

the blood is immediately mixed in a 1:2 ratio with ice-cold 8%iger perchloric acid. Further processing and sample dispatch takes place in the paediatric laboratory.

Lymphocyte vacuoles or inclusion bodies
Native smears are required for the determination of lymphocyte vacuoles. The paediatric laboratory must be informed by telephone in good time.

The collected native blood is handed over to the biomedical analyst, who immediately prepares several smears.

Ammonia
EDTA tubes must be stored on ice immediately after collection and dispatched in the same way. An ice machine is located in the paediatric laboratory and the ice can be collected there.

The removal of ammonia should before other tubes.

PFA
A telephone appointment with the paediatric laboratory is required for the PFA analysis. The blood sample for the PFA analysis must be unstowed must be carried out. Only venous sample material can be processed.

A new puncture must be made for the PFA analysis.

Procedure:
1. request a special PFA monovette from the paediatric laboratory

2. after the vein has been punctured, first take a serum monovette, this can be discarded if not required

3. fill the PFA monovette exactly to the mark

4. carefully tilt the tubes after removal

5. label the removed PFA monovette with the barcode

6. the tube must be brought to the paediatric laboratory in person within 15 minutes (not by pneumatic tube) are

Hb electrophoresis
Hb electrophoresis is carried out at Aarau Cantonal Hospital. The analysis can be recorded in i/med (Haematology USB/HB electrophoresis Aarau) and the sample material can be sent to the USB by pneumatic tube.

Notes:

A complete blood count (CBC) must also be requested for the paediatric laboratory (UKBB). The cumulative findings (CBC) are printed out by the ward / department and sent to the USB with the sample material.

 

Removal from external accesses and port catheters
Tapping from the pipe is generally permitted, but special precautions must be taken.

  • Discard at least 3 ml of blood to avoid dilution effects
  • If a medication has been administered, do not take blood from the same access immediately afterwards
  • Analyses for coagulation may NEVER can be taken from the access
  • If capillary blood sampling is to be performed after heparin administration, wait at least 30 minutes, or at least 60 minutes if the body weight is low (< 10kg)

Liquor
The sample is taken in several portions in sterile tubes. Due to the rapid lysis of cellular components in the CSF, it is essential that the material is transported to the laboratory immediately after collection, otherwise it is not possible to correctly determine the cell count or differentiate the cells.

The cell count and cell differentiation cannot be determined from coagulated CSF.

Stool (only for OBTI test and Apt test)
Collection of the test material: Deposit the faeces without urine in a clean container (bedpan or similar). Take a bean-sized amount using the spoon of the faeces tube. For liquid faeces, transfer approx. 3 - 5 ml sample into the container.

Apt test
The Apt test can be carried out from vomit or faeces. The material must be visibly bloody (fresh red colour).

Incoming sample material is checked by the paediatric laboratory for clear criteria.

Some pre-analytical errors cause the samples not to be processed. Non-processing of the samples can be caused by

  • Unlabelled sample material
  • Patient mix-ups
  • Faulty test material
  • Too little sample material
  • Inaccurate filling volume
  • Coagulated samples

In such cases, the client will be informed by telephone. The type of complaint with a visa of the BMA concerned is indicated in the findings.

In the case of other pre-analytical errors that suggest a change in the analysis results, the results are transmitted and labelled with a note. The additional information: "Value with reservation" or "Results questionable" indicates that a further blood sample is recommended to check the results.

Examples:

  • Sample clotted
  • Sample material in short supply

All errors are documented in the laboratory and analysed regularly. We will inform you of the results of this evaluation. With this measure, we want to involve all stations in order to reduce pre-analytical errors. The aim is to prevent sources of error in connection with analysis results. The well-being of the patient is our top priority!

Patient mix-ups
Mixing up patients when taking blood samples is one of the biggest sources of error. It is therefore important to find out the correct identity of the patient when taking the sample. Please make sure that the patient's name is correct. Only label the sample tubes when taking the blood sample and not before, as this could lead to confusion.

Haemolytic samples
Haemolysis is in most cases a sign of poorly performed blood collection. Analyses cannot be performed on haemolytic samples; in the paediatric laboratory this only applies to coagulation, as we do not offer any other determinations from plasma. In the case of haemolysis, it is also very likely that the blood in the tube has also coagulated and the coagulation factors have already been used up. "Slightly" haemolytic samples are submitted with the note: "Slightly haemolytic".

Coagulated samples
Coagulated samples also indicate that the blood sample was not taken properly. Make sure to mix the tube well after blood collection and do not overfill tubes. It is not possible to process an order with a coagulated sample.

We inform the client by telephone.

Incorrect filling volume
For coagulation tests and erythrocyte sedimentation rates, the tubes must be filled to the mark for correct determination. The ratio between citrate and blood must be exactly 1:10 for coagulation and exactly 1:5 for ESR. Tubes that are overfilled or underfilled with a deviation >10% cannot be processed by us. The client will be informed by telephone.

Special case: EDTA incompatibility of the thrombocytes
There are patients in whom the platelets agglutinate after some time in the blood collection tube in the presence of EDTA. These platelet aggregates are not recognised as platelets by the analysis devices, which leads to falsely low platelet values. This phenomenon is called "pseudothrombocytopenia". If pseudothrombocytopenia is suspected, the determination from a blood collection tube should be repeated with a different anticoagulant. Both an EDTA and a lithium heparin should be taken again. In this case, we will inform you by telephone and ask you to send both tubes to the paediatric laboratory immediately after collection.

Changes in sample properties can occur in the time between sample collection and sample analysis. For this reason, there is a defined sample stability for each sample and analysis. The analysis must be carried out within this period. For this reason, we ask you to send the sample material as quickly as possible.

The most common causes of changes in sample quality are

  • The metabolism of blood cells
  • Evaporation/sublimation
  • chemical reactions
  • osmotic processes
  • Lighting effects
  • Gas diffusion

The respective sample stabilities are documented in the chapter: "Analyses of the paediatric laboratory".

Examined samples are stored in the paediatric laboratory for a period of time defined for the respective analysis and sample type. Information on storage times and whether any repeat orders or repeat tests are possible can be obtained from the laboratory by telephone.

Training in capillary blood collection

Blood gases training

Or on the Easylearn learning platform: https://easylearn.ukbb.ch/ under learning offer:

- Capillary blood sampling

- Carrying out blood gas analyses at the ABL

- The measurement of the C-reactive protein on the Afinion

- Measuring urine on the Cobas U 411

- The measurement of haemoglobin A1c on the (HbA1c) on the DCA Vantage

Result output

1. routine analyses

  • within 2 hours (depending on workload)
  • Microscopic differentiation within 24 hours

2. emergency analyses

  • within 1 hour
  • Microscopic differentiations within 90 minutes, unless complex questions are involved

3. emergency analyses outside of normal operation

  • within 1 hour
  • Microscopic differentiations must be announced by telephone by the responsible OA, otherwise they will be carried out the following day.

The paediatric laboratory will repeat analyses without being asked and immediately whenever abnormalities occur and sufficient sample material is available.

We recommend a new sampling, with a new sample request, if there are still general doubts about the result even after repetition, e.g. due to possible sampling errors that could not be clarified in advance or interfering factors in the sample material.

In such cases, the findings are provided with corresponding text modules.

Standard values are also referred to as Reference values are designated. They are mainly used in laboratory medicine in order to be able to categorise measured values and thus provide an orientation as to whether a parameter is pathological (abnormal) or not.

Reference values are age- and gender-dependent and often depend on factors such as methods, reagents and equipment.

Wherever possible, our reference intervals are adapted to these factors.

The gender and age-specific reference values are automatically indicated on the report.

Reports of findings are available to internal clients in electronic form and rarely in written form (osmotic resistance).
Only when the results have been medically validated in the LIS, i.e. checked for plausibility and approved, are the electronic findings reports automatically generated as PDFs in i/med and the written findings created.

Please note that laboratory results are confidential patient documents that are subject to data protection. They may only be viewed by the attending physician or consultant.
Reports of findings must be disposed of separately (disposal of data protection).
The forwarding of diagnostic reports to external doctors (e.g. GPs) is only possible with the patient's consent (exception: referring doctor).
For external senders, the report of findings is sent by fax and A Mail.

Alarm values, i.e. laboratory results that could lead to critical, life-threatening events, are always communicated by telephone and transmitted electronically at the same time.

Clinical studies

Before you start a study or scientific work, plan your study with all those involved. Follow the instructions on the page: Home > Research.

The paediatric laboratory will be happy to advise you on planning laboratory diagnostics at the UKBB.

Please bear in mind that the analyses to be carried out by the paediatric laboratory must be organised in such a way that we can maintain daily routine operations without restrictions.

To help us achieve this, we ask you to observe the following rules:

  • The registration of new studies with laboratory orders must be submitted to the UKBB laboratory management (Brigitte Baumgartner or Prof Dr Nicolas von der Weid) take place
  • A detailed description of the desired analyses must be available
  • The test subjects must be recorded in SAP from outpatient admission as service patients (including visits)
  • Please note that it is possible to create lab profiles via the Help Desk
  • Laboratory orders must be recorded in i/med by the instructed nurse, study nurse or doctor as follows:
  1. Patient (search)
  2. Specify withdrawal date and time
  3. Institute UKBB
  4. Nursing OU ward (e.g. neuropol. or ward A)
  5. Subject OU 70 for teaching and research, or 71 for contract research (outpatient and inpatient)
  6. Physician (Head of Research UKBB)
  7. Comment tick study
  8. Enter study name, visit and/or time under Remarks
  9. Select the corresponding profile or analyses (laboratory analyses for POCT devices are recorded with the SAP science case number on the device)
  • The findings are transmitted electronically.
  • Analyses are billed in the same way as patients
  • The guarantor is the UKBB
  • The time spent in the paediatric laboratory is invoiced in IBIcare

All persons in the paediatric laboratory who are involved in any way in a clinical study are subject to a duty of confidentiality. Absolute confidentiality is maintained.

Analyses of the paediatric laboratory

Here you will find an alphabetical list of the paediatric laboratory's analyses.

The smallest possible volume of the corresponding microvette or monovette is always specified as the volume.

Method:

microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri by telephone arrangement

Material:

Secretions from pustules or skin rashes

Sample treatment:

  • Swabs are obtained from pustule contents or other skin rashes
  • The attending physician prepares the swab preparations, the BMA is present

Volume:

If possible, several smears are made

Reference range:

Customised

Remark/special feature:

Clinical information required

Reorder:

Not applicable

Synonym:

Heparin activity, heparin therapy, factor anti-Xa activity

Method:

chromogenic / photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml or 1 ml

Reference range / therapeutic areas:

  • < 0.1 IU/ml (not treated)
  • 0.6 - 1.0 IU/ml (with 2x daily heparinisation in the therapeutic range)
  • 0.4 - 0.6 IU/ml (in the prophylactic range)
  • 0.5 - 1.0 IU/ml (for newborns in the prophylactic range)

Reorder:

4 h

Remark/special feature:

The anti-Xa activity method is offered in the paediatric laboratory for testing low molecular weight or fractionated heparin (NMW) and high molecular weight or unfractionated heparin (UFH).

When requesting an order in i/med, it is essential to select the correct therapy.

Synonym:

Heparin activity, heparin therapy, factor anti-Xa activity

Method:

chromogenic / photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml or 1 ml

Reference range / therapeutic areas:

  • < 0.04 IU/ml (not treated)
  • 0.3 - 0.7 IU/ml (therapeutic range)

Reorder:

4 h

Remark/special feature:

The anti-Xa activity method is offered in the paediatric laboratory for testing low molecular weight or fractionated heparin (NMW) and high molecular weight or unfractionated heparin (UFH).

When requesting an order in i/med, it is essential to select the correct therapy.

Availability:

Mon-Fri and emergency

Material:

Vomit/stool

Volume:

Stool: Bean-sized portion or approx. 3 - 5 ml sample for liquid material

Reference range:

negative

Remark/special feature:

Only possible with visibly bloody stools (fresh, red blood)

Method:

coagulometric / photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml or 1 ml

Reference range:

20-45 sec

Therapeutic areas:

68-80 sec

Reorder:

4 h

Method:

according to Westergren

Availability:

Mon-Fri and emergency

Material:

Monovettes: Na citrate 1:5 grey

Microvettes: Na-citrate 1:5 violet

Sample treatment:

Fill the capillary of the microvette end-to-end (free of air bubbles)

Fill the monovette exactly to the mark

The sample must be in the paediatric laboratory no later than 2 hours after collection

Volume:

Monovette: 2 ml, Microvette: 200 µl

Reference range:

Macro lowering: 0-10 mm /h

Micro subsidence: 0-10 mm/ h

Method:

cytochemical

Availability:

Mon-Fri by telephone appointment

Material:

EDTA whole blood monovettes: violet, microvettes: violet

CSF native

Slide smears EDTA

Slide smears Native

Bone marrow smears native

CSF smears native

Sample treatment:

External senders: Send EDTA blood to the paediatric laboratory within 2 hours (smears must be prepared within 2 hours of blood collection)

Volume:

EDTA: Monovette: 1.2 ml, Microvette: 0.2 ml

Blood/bone marrow, 2-4 smears each

Cerebrospinal fluid: 1 smear

Reference range:

Individual see report of findings

Remark/special feature:

Clinical information required

Reorder:

2 h (smears must be prepared within 2 h), if smears are already available, they can be reordered for iron colouring for up to several months

Method:​​​​​​​

Resistance measuring principle, hydrodynamic focussing

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request i/med: CBC or complete blood count

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

6 h

Method:

Coagulometric / Photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml or 1 ml

Reference range:

1.7 - 4.1 g/l

Reorder:

4 h

Method:

Microscopically (counting of fragmentocytes per 1000 erythrocytes)

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Native smears (by paediatric laboratory)

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.3 ml

Reference range:

negative (exception: premature babies)

Reorder:

6 h

Synonym:

Haematogram V

Method:

Photometric, resistance measurement principle, fluorescence flow cytometry, hydrodynamic focussing

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: The sample material must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks/Special features:

The flags transmitted by the device apply merely as indications, not as findings.

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

6 h (Attention! Microscopic differentiation 2 h)

Method:

Resistance measuring principle, hydrodynamic focussing

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

6 h

Method:

Photometric

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on age group and gender, see findings report

Reorder:

6 h

Synonym:

Haematogram II

Method:

Photometric, resistance measurement principle, fluorescence flow cytometry, hydrodynamic focussing

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: The sample material must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

6 h for automatic differentiations

2 h for microscopic differentiations

Method:

Fluorescence flow cytometry

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.3 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on age group and gender, see findings report

Reorder:

6 h

Method:

Microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri by telephone appointment

Material:

Native smears (by paediatric laboratory)

Volume:

At least 3 smears

Reference range:

neg

Remark/special feature:

Native smears are required for the determination of lymphocyte vacuoles The paediatric laboratory must be informed by telephone in good time

​​​​​​​Method:

calculated

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on age group and gender, see findings report

Reorder:

6 h

​​​​​​​Method:

calculated

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on age group and gender, see findings report

Reorder:

6 h

Method:

calculated

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: EDTA whole blood must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individual depending on age group and gender, see findings report

Reorder:

6 h

Method:

microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

External sender: Native smears

Sample treatment:

External senders: Smears for microscopic differentiation must be prepared within 2 hours after blood collection

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

2-4 smears

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

2 h (Smears must be prepared within 2 h, smears are often available and are stored for 6 days. Please inform yourself by telephone)

Method:

microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri by telephone appointment

Outside office hours only with telephone registration of the senior physician

Material:

Bone marrow smears native

Sample treatment:

The smears are prepared by the BMA directly during the puncture

Volume:

Depending on the material and diagnosis, between 15 and 40 smears are made

Reference range:

Customised, see Bone marrow reference values

Remark/special feature:

Clinical information required

Always order GBB with microscopic differentiation and reticulocytes (should be available from the same day or previous day)

Method:

microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri and emergency

Material:

Native CSF

Sample treatment:

Depending on the indication, between 2 and 6 cerebrospinal fluid preparations are produced

Volume:

At least 0.5 ml

Reference range:

Leukocytes 0-10 µl / (of which 90% lymphocytes)

Erythrocytes 0/ µl

Remark/special feature:

  • Due to the rapid lysis of cellular components in the CSF, it is essential that the material is transported to the laboratory immediately after collection, otherwise it is not possible to correctly determine the cell count or differentiate the cells.
  • No determination should be made from clotted CSF (with a visible clot); we will contact the attending physician.
  • A microscopic differentiation of the blood count should always be ordered promptly.

Reorder:

1h (The smears must be prepared within 1h, smears are often available. Please call for more information).

​​​​​​​Method:

microscopic (May-Grünwald-Giemsa staining)

Availability:

Mon-Fri and emergency

Material:

Native punctate fluid

Punctate fluid in EDTA

Sample treatment:

Depending on the material quality, several punctate preparations are produced

Volume:

At least 0.5 ml

Reference range:

Normal punctates are low in cells. The following guide values apply to joint punctates:

Normal: Leucocytes: 50-100/ µl

Non-flammable: 200-1000/ µl

Inflammatory: >3000/ µl

Differentiation:

Lymphocytes: 24 %

Monocytes: 48 %

Granulocytes: 7 %

Remark/special feature:

  • Due to the rapid lysis of cellular components in the punctate, it is essential to transport the material to the laboratory immediately after collection, otherwise a correct determination of the cell count and cell differentiation is not possible
  • Cell count and cell differentiation cannot be determined from clotted punctate

Reorder:

2 h

Smears are often available and are kept for 6 days, please contact us by telephone.

Synonym:

Occult test

Method:

Immunochromatography

Availability:

Mon-Fri

Material:

Native chair

Volume:

Bean-sized portion

Reference range:

negative

Remark/special feature:

- Samples from patients with bleeding (haemorrhoids, menstruation) should not be used.

- Alcohol abuse, treatment with aspirin, indomethacin, phenylbutazone, corticosteroids and reserpine can lead to gastrointestinal bleeding.

- Polyps and colorectal tumours can bleed intermittently.

Method:

Lysis before and after incubation

Availability:

Mon-Thu by appointment by telephone

Material:

Heparin whole blood, monovettes green

For GBB with microscopic differentiation and reticulocytes: EDTA whole blood, monovettes/microvettes violet

Volume:

Heparin whole blood: 2 x 1.2ml

EDTA whole blood: monovette: 1.2 ml, microvette: 0.2 ml

Remark/special feature:

  • GBB with microscopic differentiation and reticulocytes always prescribed
  • The determination of osmotic resistance is only useful from the age of 6 months

​​​​​​​Method:

cytochemical

Availability:

Mon-Fri by telephone appointment

Material:

EDTA whole blood monovettes: violet, microvettes: violet

CSF native

Native punctate

Slide smears EDTA

Slide smears Native

Bone marrow smears native

CSF preparation native

Punctate preparation native

Sample treatment:

External senders: Send EDTA blood to the paediatric laboratory within 2 hours (smears must be prepared within 2 hours of blood collection)

Volume:

EDTA: Monovette: 1.2 ml, Microvette: 0.2 ml

Blood/bone marrow, 2-4 smears each

Cerebrospinal fluid/spot, 1 smear each

Reference range:

Individual see report of findings

Remark/special feature:

Clinical information required

Reorder:

2 h (smears must be prepared within 2 h); if smears are already available, they can be reordered for PAS staining for several months.

Synonym:

Platelet function test

Method:

Closure time in vitro after platelet adhesion to collagen/epinephrine, collagen/adenosine diphosphate

Availability:

Mon-Fri

Material:

Buffered citrated whole blood, turquoise monovette

Sample treatment:

Sample must be brought to the laboratory (do not send by tube post)

Volume:

Monovette: 3.8 ml

Remarks/Special features:

The blood sample for the PFA analysis must be unstowed is performed. After the vein has been punctured, a serum monovette is taken first. For detailed instructions, see chapter: Preanalytics/ Special analysis and acceptance procedure/PFA

Reference range:

Collagen/epinephrine 84-160 sec Collagen/adenosine diphosphate: 68-121 sec

Method:

Potentiometric, amperometric, absorption spectometric

Availability:

Mon-Fri and emergency

Material:

Heparinised blood gas syringe

Heparinised blood gas capillaries

Sample treatment:

Perform analysis from blood gas syringe within 30 min, perform analysis from blood gas capillary immediately

Volume:

Syringe: 0.5- 2 ml, capillary: 100 (ABL) 200 µl (Cobas)

Reference range:

Depending on age, material and method, see Radiometer reference values

Remark/special feature:

The default settings of the devices:

Emergency:

pH, pCO2, pO2, Hb, SO2, Na, K, Cl, Gluc, Lac (capillary FLEXMODUS)

Alternatively selectable: Gluc, Lac (capillary glu/lac)

Alternatively selectable: pH, pCO2, pO2, Hb, SO2, MetHb, COHb, O2Hb (capillary 55 µl)

Alternatively selectable: pH, pCO2, pO2, Hb, SO2, Na, K, Cl, Gluc, Lac, MetHb, COHb, O2Hb, HHb (intoxication capillary)

IPS/NEOFK

pH, pCO2, pO2, Hb, SO2, MetHb, COHb, HHb, HbF, Na, K, iCa, Cl, Gluc, Lac, Bili (plastic calibre 95 µl)

Alternatively selectable: pH, pCO2, pO2, Hb, SO2, Bili, (capillary 55 µl)

OPS

pH, pCO2, pO2, tHb, SO2Na, K, Ca++, Cl, Gluc, Lac, MetHb, COHb, O2Hb, HHb

Alternatively selectable: pH, pCO2, pO2, Hb, SO2, Na, K, Cl, Gluc, Lac (capillary FLEXMODUS)

Alternatively selectable: pH, pCO2, pO2, Hb, SO2, MetHb, COHb, O2Hb (capillary 55 µl)

Microclots and air interfere with the blood gas analysis. No measurement is possible. ​​​​​​​

Reorder:

not possible

Method:

immunochemical

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood, monovette/microvette violet

or

Lithium heparin whole blood or plasma, monovette/microvette light green

or

BGA capillary

Volume:

Fill the 1.5 µl glass capillary from the material above

Reference range:

< 10 mg/L

Remark/special feature:

  • Attention: As soon as the capillary is filled with sample material, the test cassette must be analysed within 1 minute be started. If the test cassette is stored for too long before being analysed, the sample material may dry out or coagulate, in which case an error message is displayed.
  • As an acute-phase protein, CRP is elevated in bacterial infections and inflammations. Viral defects only lead to a minimal increase. If the HCT values are outside the range of 20 to 60% (e.g. in newborns), no CRP result is displayed. In these cases, plasma should be used for CRP determination. In this case, send the EDTA whole blood to the laboratory by telephone arrangement
  • Reorder:

2 days

Method:

Absorption spectrometric

Availability:

Mon-Fri and emergency

Material:

Heparinised blood gas syringe

Heparinised blood gas capillaries

Sample treatment:

Perform analysis from blood gas syringe within 30 min, perform analysis from blood gas capillary immediately

Volume:

Syringe: 0.5- 2 ml, capillary: 100 (ABL) 200 µl (Cobas)

Reference range:

Remark/special feature:

  • Emergency ward: Hb derivatives must be dialled before the blood gas analysis (intoxication)
  • Microclots and air interfere with the blood gas analysis. No measurement is possible

Reorder:

not possible

Method:

photometric

Availability:

Mon-Fri

Material:

EDTA whole blood, monovette/microvette violet

or heparin whole blood, monovette/microvette green

Volume:

Filling the 1 µl glass capillary from 1.2 ml EDTA whole blood (monovette) or from 0.2/0.5 ml EDTA whole blood (microvette) or from 1.2 ml heparin (monovette) or from 0.5 ml heparin (microvette)

Reference range:

Normal range: 3-6 %

Diabetics with diabetes: 6-8 %

Poorly controlled diabetics: -20 %

Remark/special feature:

  • The sample material for filling the capillary can also be obtained directly from the finger puncture (EDTA or heparin collection is recommended if repeat measurements are required)
  • ATTENTION: As soon as the sample is filled into the glass capillary, the analysis must start within 5 minutes
  • Measuring the HbA1c concentration is recommended for the long-term treatment of diabetes patients
  • Reorder:

2 days

Method:

Test strips (photometric evaluation)

Availability:

Mon-Fri and emergency

Material:

Urine

Monovette yellow

Volume:

Monovette: 10 ml or beaker

Reference range:

SG 1.015-1.025

pH 4.8-7.4

LEU neg

NIT neg

PRO neg

GLU standard

KET neg

UGB standard

BIL neg

ERY neg

Remark/special feature:

Use fresh urine, instruct the patient precisely regarding the collection of midstream urine

Reordering/stability:

2 h

Synonym:

Myeloperoxidase

Method:

cytochemical

Availability:

Mon-Fri by telephone appointment

Material:

EDTA whole blood monovettes: violet, microvettes: violet

Slide smears EDTA

Slide smears Native

Bone marrow smears native

Sample treatment:

External senders: Send EDTA blood to the paediatric laboratory within 2 hours (smears must be prepared within 2 hours of blood collection)

Volume:

EDTA: Monovette: 1.2 ml, Microvette: 0.2 ml

Blood/bone marrow, 2-4 smears each

Reference range:

Individual see report of findings

Remark/special feature:

Clinical information required

Reorder:

2 h (smears must be prepared within 2 h), if smears are already available, they can be reordered for POX staining within 2 days

Synonym:

Thromboplastin time

Method:

Coagulometric / photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml

Reference range:

70 – 120 %

Therapeutic area

See INR value

Reorder:

4 h

Method:

Coagulometric / Photometric

Availability:

Mon-Fri and emergency

Material:

Citrate plasma, monovettes/microvettes light blue

Sample treatment:

Carefully mix the sample tubes immediately after removal.

The sample tube must be filled exactly to the mark.

External senders: The sample material must arrive at the paediatric laboratory within 4 hours.

Volume:

Monovette: 1.2 ml, Microvette: 0.5 ml or 1.0 ml

Reference range:

0.9-1.1

Therapeutic area:

2-3 depending on indication

Remark/special feature:

With oral anticoagulation

Reorder:

4 h

Method:

Fluorescence flow cytometry

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: The sample material must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Reference range:

Individual depending on parameters, age group and gender, see findings report

Reorder:

6 h

Method:

cytochemical

Availability:

Mon-Fri by telephone appointment

Material:

EDTA whole blood monovettes: violet, microvettes: violet

Liquor Native

Native punctate

Slide smears EDTA

Native slide smears

Bone marrow smears native

CSF preparations native

Punctate preparation native

Sample treatment:

External senders: Send EDTA blood to the paediatric laboratory within 2 hours (smears must be prepared within 2 hours of blood collection)

Volume:

EDTA: Monovette: 1.2 ml, Microvette: 0.2 ml

Blood/bone marrow, 2-4 smears each

Punctate/cerebrospinal fluid, 1 smear each

Reference range:

Individual see report of findings

Remark/special feature:

Clinical information required

Reorder:

2 h (smears must be prepared within 2 h); if smears are already available, they can be reordered for acid phosphatase staining for up to 24 h

Method:

Microscopy of a blood preparation produced under oxygen deprivation

Availability:

Mon-Fri by telephone appointment

Material:

Fresh EDTA whole blood

Monovettes: violet, microvettes: violet

Volume:

EDTA: Monovette: 1.2 ml, Microvette: 0.2 ml

2-4 blood smears each

Reference range:

negative

Remark/special feature:

Haemoglobin electrophoresis is recommended if sickle cells are detected and sickle cell anaemia is suspected

Reordering/Sample stability:

24 hours after removal

Method:

Resistance measurement principle, fluorescence flow cytometry

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Sample treatment:

External senders: The sample material must arrive at the paediatric laboratory within 6 hours

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Remarks:

Request in i/med: CBC or complete blood count

Reference range:

Individualised depending on age and gender, see findings form

Reorder:

6 h

Method:

Resistance measuring principle

Availability:

Mon-Fri and emergency

Material:

EDTA whole blood

Monovettes: violet

Microvettes: violet

Volume:

Monovette: 1.2 ml, Microvette: 0.2 ml

Reference range:

Customised according to indication

Remark/special feature:

After platelet concentrate administration, the platelet 10-minute value is determined in order to monitor the increase; only the platelet count may be used from the results of the small blood count.

​​​​​​​Method:

microscopic (May-Grünwald-Giemsa)

Availability:

Mon-Fri by telephone arrangement

Material:

Different tissues or organs

Volume:

If possible, several preparations are made

Remark/special feature:

The paediatric laboratory must be informed in good time by telephone if swab preparations are to be made. The BMA produces the swab preparations.

Clinical information required

Reorder:

Not applicable

Method:

Chamber counting

Fluorescence flow cytometry (for cell-rich cerebrospinal fluid)

Availability:

Mon-Fri and emergency

Material:

Native CSF

Sample treatment:

  • Due to the rapid lysis of cellular components in the CSF, it is essential that the material is transported to the laboratory immediately after collection, otherwise it is not possible to determine the cell count correctly
  • The cell count cannot be determined from clotted CSF

Volume:

At least 0.5 ml

Reference range:

Leucocytes (age: 1 day - 1 month): 0-10 /µl

Leukocytes (age: > 1 month): 0-5 /µl

Erythrocytes 0/ µl

Remark/special feature:

Clinical information required

The erythrocytes are given in steps of 1000 in the automatic cell count

Reorder:

CSF must be sent to the paediatric laboratory immediately after collection. The cell count should be performed within 30 minutes.

Method:

Chamber counting

Fluorescence flow cytometry (for cell-rich punctate)

Availability:

Mon-Fri and emergency

Material:

Native punctate fluid

Punctate fluid in EDTA

Sample treatment:

  • Due to the rapid lysis of cellular components in the punctate, it is essential that the material is transported to the laboratory immediately after collection, otherwise a correct determination of the cell count is not possible
  • The cell count cannot be determined from coagulated punctate

Volume:

At least 0.5 ml

Reference range:

Normal punctates are low in cells. The following guide values apply to joint punctates:

Normal: Leucocytes: 50-100/ µl

Non-flammable: 200-1000/ µl

Inflammatory: >3000/ µl

Remark/special feature:

Clinical information required

The erythrocytes are given in steps of 1000 for the automated cell count

Reorder:

2 h

Tables

Device comparisons
For current comparative values of test results between different laboratory devices, please contact the laboratory by telephone.

Table for conversion to SI units

List of criteria for a microscopic differential blood count

Alarm value list

Morphological assessment of the differential blood count

Information on measurement uncertainties can be obtained by calling the laboratory.

Failure concept

The failure concept is intended to ensure that laboratory medical services can be carried out smoothly even during system failures. To simplify the procedure for nursing staff, we have summarised the most important points.

Procedure in the event of system failures (failure concept)

Forms

USB form Application for cancellation of a laboratory order (ONLY FOR USB)

Paediatric laboratory order form (For external senders and in case of system failure (can be filled in electronically -> select download)

Capillary blood collection at UKBB

Form Missing analyses in i/med (If the file does not open -> select download -> save document)

Form POCT analyses during system failure (can be filled in electronically, please click on the blue "open" button at the top left and select "open in browser" after you have opened the document).

Counselling hotline for child and youth emergencies

The Medgate Kids Line provides quick and uncomplicated medical advice if your child is unwell. The medical team of our partner Medgate is available to you by telephone around the clock.

058 387 78 82
(billing via health insurance)

For emergencies abroad: Call the emergency number of your health insurance company. You will find this number on your health insurance card.

More information: On the Page of the emergency ward you will find everything you need to know about behaviour in emergencies, typical childhood illnesses and waiting times.

Important emergency numbers

144 Outpatient clinic
145 Tox Info Suisse (Poisonings)
117 Police
118 Fire brigade

UKBB

University Children's Hospital Basel
Spitalstrasse 33
4056 Basel | CH

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