by Oscar Fay

In this chapter we have tried to make a synthesis of the current possibilities of the biochemical laboratory in order to offer a guide, as up-to-date as possible, that is useful to the difficult task that the doctor faces when he is in front of a patient who should attend.

For this we have made a brief review of the role that the clinical laboratory in medicine currently fulfills, how it has evolved to this day and the role that laboratory personnel play in this context. Likewise, we have highlighted the most important aspects to consider when requesting and interpreting laboratory tests.

Finally, we present in this chapter as a guide, a list of laboratory tests grouped according to the most common medical profiles or specialties that can be presented in medical practice and we provide various links to sites for online consultation of additional, more detailed information on laboratory tests and their interpretation. We have also included a table with newly emerging methodologies that promise to open our way to new paths in research and clinical practice.

Scientific technological advances in the sciences are increasingly vertiginous with a growth curve of unimaginable magnitude towards the future. Health criteria are developing a close interrelation in the biological, environmental, social and psychological aspects, which has led us to think in a comprehensive way about the relationships between living beings on the planet and human beings as individuals, who are also part of that ecosystem, insofar as they are interrelated with it. For example, from the point of view of microorganisms and their relationship with the ecological environment, with animals, plants, and people.

It is extremely difficult to predict what current technology will provide the benefits that can be reflected in solutions to global health problems.

The current approach to knowledge will have an extraordinary impact in the coming times on the subject of Medical Sciences. The horizontality and the relationships between the different disciplines allow us to envision an extraordinary impact in the coming times in Medical Sciences.

Feeling the challenge of participating with significant contributions to a complex problem requires constant updating. Biochemical professional practice also requires that commitment and leadership.

All of us who have been involved in collaborating in the delivery of this chapter, we are sorry and we have worked with the simple purpose of contributing another look, from our perspective, to the benefit and commitment to continue improving what we do.

Our gratitude to all who have collaborated with this contribution.

Bq. Ricardo Giordano (Mat. 929), Bq. Cesar Yene (Mat 1761), Dr. in Bq. Fernando Elias (44323), Coordination: Dr. in Bq. Oscar Hector Fay (0100/68)

 

What is the role of a clinical laboratory?

Analyze human biological samples that provide useful information to health teams for the study, diagnosis, prevention and treatment of different pathologies.

What is the role of laboratory personnel?

Clinical laboratory professionals are responsible for:

  • Use analytically acceptable methods and techniques in laboratories , taking care of all aspects of quality control in all its stages: pre-analytical, analytical and post-analytical, in addition to participating in external quality evaluation programs.
  • Prioritize the correct selection of tests and methodology in terms of predictive value, as well as their sensitivity and specificity and that they are clinically relevant in order to guarantee their clinical utility.
  • Eliminate unhelpful tests and those outdated that have not shown a benefit in their use and implement new tests if the evidence has proven their effectiveness.

How has the biochemical laboratory evolved in recent times?

Today's biochemical laboratory is one of the areas of diagnosis that has undergone the most changes in recent years. The availability of new technologies (see attached list of emerging technologies) coupled with increasing automation , has led to higher analytical quality, resulting in increased efficiency and safety.

Currently there are continuous flow analytical systems (absorbance photometry, turbidimetry, nephelometry, fluorescence, colorimetry, enzyme and immunoenzymatic kinetics, etc.), which consist of:

  • Sample taking and dispensing system
  • Reagent dispensing system
  • Incubation baths
  • Detectors
  • Data processor
  • Data processing software

What does automation bring?

The automation requires less operator intervention, increases productivity, with decreasing response times and greater throughput. 

These systems provide greater sensitivity, specificity, precision, and truthfulness. They require a smaller volume of samples and reagents, with high analytical performance, significantly reducing operating costs and allowing the processing of a large number of samples simultaneously. 

This requires systems that allow the handling of a large volume of data: patient admission, sampling, sample preparation and distribution, work lists, quality controls, reception and validation of results, issuance of reports, historical files with background, purchasing management and administrative management. To this is added the existence of networks where external requests are entered to the LIS, reports are issued online, with the possibility of consulting the results from any device. 

What role does the clinical biochemist play in this scenario?

The evolution of the laboratory as a consequence of technological development has improved the quality of the processes, but in this scenario, professional judgment continues to be key. In addition to a technical validation , which is the acceptance of results with technical criteria (maintenance, calibrations, quality controls, alarms issued by the autoanalyzers, Delta Check that indicates the variation with respect to the antecedents), a clinical validation is also necessary , which It involves evaluating the consistency of the data from the different tests in a request together with the patient's demographics (sex, age, etc.).

On the other hand, the greater number of tests available has led to a greater need for interaction with the clinician for the suggestion of complementary studies or for the interpretation of the data, which has substantially modified the profile of the required biochemical professional currently.

What are the factors to consider when requesting a lab test?

Evaluate whether obtaining the result would provide useful information for diagnosing or deciding on any therapeutic action that benefits the patient.

Request the laboratory tests taking into account their sensitivity, specificity, positive and negative predictive value according to the context of the patient and the pathology (s) being evaluated.

What factors should be considered when interpreting laboratory data?

- Variables preanalíticas:

It is important to take into account the existence of preanalytical factors related to the patient and others related to the activity of health personnel (doctors, nurses and laboratory personnel) that can affect laboratory results.

Some cannot be modified, so they must be known in order to properly interpret the exams; however, there are other modifiable ones with the correct sampling and preparation of patients, which are essential to obtain valid results.

Main factors not susceptible to modification that must be known in order to make a correct interpretation of the results :

  • Age
  • Sex
  • Race
  • Pregnancy
  • Phase of the menstrual cycle

Main factors susceptible to modification with the correct sampling and preparation of the patient :

  • Fast
  • Diet
  • Stress.
  • Physical activity
  • Circadian rhythm
  • Ingestion of medications.
  • Smoking habit, intake of alcoholic beverages, caffeine or other stimulant substances.
  • Surgery and intramuscular injection.

Factors dependent on health personnel:

Interferences related to the activity of health personnel (doctors, nurses, laboratory personnel, etc.) are generally due to poor compliance with operating standards. Among the most frequent are: errors in sample collection, identification and handling, delay in sending samples to the laboratory, incomplete or incorrect preparation of the patient, incomplete collection in the case of serial samples, information to the laboratory inaccurate, incomplete or illegible, etc.

- Reference values

To be able to interpret a measured value of a biological magnitude of a patient for diagnostic purposes, it is essential to know one or more values ​​of that magnitude evaluated in similar individuals and compare them.

A biological reference value is a measured value of a particular magnitude obtained for comparative purposes in an individual, called a reference individual, that meets certain pre-established requirements.

The reference values ​​always depend on the procedure used to measure it.

In clinical practice, the results are compared against fixed references, which can be:

  • Population reference values.
  • Local protocols by consensus.
  • Values ​​proposed by groups of experts.
  • Risk-based values.
  • Multiples of the reference values.

- Biological variability and analytical variability:

The values ​​obtained in the laboratory of a certain analysis in a patient vary over time due to two factors which are:

1) Biological variability

Variation of the levels of an analyte around its homeostatic point. These variations can occur throughout the day, weeks, etc., and are specific to each analyte. We can speak of “intra-individual variability” (how it varies in said patient) and “variability between individuals” (how it varies between different people).

Some characteristics that result from this are:

  • No individual has results that span the entire reference interval.
  • The results of each individual occupy a small portion of the reference interval.
  • The mean of the results of each patient falls within the reference interval and differs from that of the rest of the individuals.
  • Many individuals may have unusual values, and still be within the reference interval.
  • Some individuals randomly have values ​​inside and outside the reference interval.
  • Stratification of the reference values ​​(by age, sex, cycle time) makes them more useful for monitoring and diagnosis.

2) Analytical variability

Not all the measurement procedures available to measure a quantity are subject to the same metrological variability, so most measurement procedures lead to different results.

Each time a determination is repeated, it will yield results that are normally distributed around a central value. The amplitude of the dispersion of these values ​​is measured through random error. Laboratories know the magnitude of said dispersion through the evaluation of quality controls, this being another contribution to the variability of a patient's results.

What tests to request for each pathology?

In the current state of clinical biochemistry, the universe of available tests is very wide and complex. An approach strategy for the selection of laboratory tests in different clinical situations, consists of approaching through profiles according to the following table:

Analytical Profiles Lab tests
Health status Platelet
blood count Erythrosedimentation Blood
glucose
TSH
Uremia
Uricemia
Creatininemia
TGO (ASAT)
TGP (ALAT)
GGT
Alkaline phosphatase
Cholesterol
HDL
LDL
Triglycerides
Total
proteins Calcium phosphorus - Sodium - Serum potassium
Full urine
Preoperative CBC with platelets
Clotting Time
Bleeding time
Prothrombin time (PT)
KPTT
Glycemia
Cholinesterase serum
Uremia
creatinine
HIV-HBsAg-HCV
Blood type and Rh factor
Urine complete
Anemias Hemogram
Reticulocyte count
Sideraemia
% Transferrin saturation
Folic acid
B12
Serum transferrin Serum
ferritin
HB electrophoresis
Molecular studies for hemoglobinopathies 
Diabetes Basal glycemia and post glucose load 120 min
insulin basal and post glucose load 120 min
Curve glucose tolerance
HbA1C
Fructosamine
Insulin
C - peptide
Ac anti-insulin (AII)
Ac anti tyrosine phosphatase IA2 membrane
Ac anti-pancreatic Islets ( ICA)
Ab anti-glutamic acid decarboxylase (GADA)
Microalbuminuria
Complete urine
Creatinine clearance
Glomerular filtration rate (TGF)
Ions and acid base state Acid Base Status (EAB)
Sodium
Potassium
Chloride
Calcium
Magnesium
Phosphorus
Rheumatoid arthritis Hemograma
Erythrosedimentation
Urico
ASO
VDRL
Ac anti-cyclic citrullinated peptide (CCP)
Rheumatoid Factor (RF)
Rosse Ragan
Factor antinuclear (ANA)
C-reactive protein (CRP)
antibodies against antigens nuclear removable (ENA)
anti-DNA
Therapeutic drug monitoring Carbamazepine
Cyclosporins
Phenytoin
Valproic
Digoxin
Phenobarbital
Theophylline
Vancomycin
Amikacin
Gentamicin
Oxcarbazepine
Lithium
Tacrolimus
Methotrexate
Cancer Tumor markers PSA / PSA Free
CA 19.9
CA 15.3
CA 125
CA-72.4
Carcinoembryonic antigen (CEA)
HE4
Alpha fetus protein
Beta-HCG
Calcitonin
Chromogranin A
Beta-2-microglobulin
CYFRA 21-1
Specific neuroenolase (NSE)
Thyroglobulin
Metanephrine
5-hydroxy-indoleacetic acid (urine)
Mandelic vanillin acid (urine)
Liver function Transaminsases (GOT and GPT)
Gamma glutamyl transferase (GGT)
Alkaline phosphatase
Cholinesterase
Total and Fractionated Bilirubin
Prothombin Time (PT)
Factor V
Lactic Dehydrogenase (LDH))
Total and Fractionated Proteins
Viral serology for hepatitis: (Hepatitis A, B, C, D, E)
Autoimmune hepatitis type I: (anti-ACTIN)
Antibodies directed against Ags of smooth muscle cells: actin
Autoimmune hepatitis type II: (anti-LKM1 and anti-LKM2)
Antibodies that react against the cytoplasm of hepatocytes and renal tubule proximal (anti-liver kidney microsome:
LKM-Cytochrome P-450 Antigen
Cardiovascular risk factors Total cholesterol
TG
Col-HDL
Col-LDL
Apo B
Apo A1
Apo B / Apo A1
Lp (a)
Homocysteine
Lp-PLA2
Ultrasensitive CRP
Fibrinogen
Vitamin D
Cardiac Troponin I
Troponin T
Ultrasensitive troponin
CPK / LDH / TGP / TGO
CPK-MB
Myoglobin
Sodium-Potassium-Chloride
NT-proBNP
Renal Hemogram
Erythrosedimentation
Urea
Calcium- phosphorus
Creatinine
Creatinine clearance
Sodium-Potassium-Chloride
Creatinine Clearance
Glomerular Filtration Rate
N-GAL
Proteinogram electrophoretically
Proteinuria 24 hours
Electrophoresis 24 hour urine
count Addis
Albumin
Albumin in urine and ratio albumin / creatinine urine
Protein in urine and protein / creatinine ratio in urine Urine
culture
Beta-2-microglobulin
Acid-base status
Nephrolithiasis Calcemia
Ionic calcium
Phosphatemia
Magnesemia
Creatininemia
Uremia
Uricemia
Calciuria
Phosphaturia
Urine magnesium
Uricosuria
Citraturia
Oxaluria
Tubular phosphorus reabsorption
Crystallographic and bacteriological examinations
Arterial hypertension To the renal profile add:
Renin
Aldosterone
Plasma catecholamines
Adrenaline and noradrenaline in urine
Angiotensin converting enzyme (ACE)
Muscular CK
CK MM
LDH
Aldolase
Creatine
Myoglobin in serum
Myoglobin in urine
ACRA anti-acetylcholine receptor antibodies (Myasthenia gravis)
Anti-skeletal muscle antibodies
Malabsorption syndrome Fat malabsorption Van de Kamer test, Sudan III stain, Acid steatocrit, Nira, Labeled triolein test, 13C-MTG test, Fluorescein dialurate test.
Carbohydrate malabsorption Glycemia curve after H de C overload
D-xylose
test Lactose intolerance
test Breath test
Protein malabsorption Quantification of fecal nitrogen
Alpha-1-antitrypsin clearance
test Citrulline and arginine test
Study of malabsorption of vitamin B, bile salts
Bacterial overgrowth tests
Test of exogenous pancreatic function.
Enf. celiac Ac. anti-Gliadina (AGA) IgA and IgG
Ac. anti-Gliadina deaminada (ADGP) IgA and IgE
Ac. anti-Endomission (EMA) IgA and IgG
Ac. Tissular anti-Transglutaminase (ATGt) IgA and IgE
HLA class II-DQ (DQ2-DQ8) gene specification
Gastrointestinal disorders Inflammatory Bowel Disease: Crohn's Disease / Ulcerative Colitis C. anti-Saccharomyces cereviseae (ASCA) IgA of IgG
Diagnosis of viral diseases HIV Acs HIV1 / 2
Western Blot
Viral Load
Genotype
Resistance
test
HLA B5701 tropism test
Hepatitis A anti-HVA (IgM)
anti-HVA (IgG)
Hepatitis B Hbeg
HbsAg
Anti-HBc IgG
Anti-HBc IgM
Anti-HBe
Anti-HBs
Hbs Ag quantitative
Ab. Anti-HBVCORE (IgG) (Blood Bank Serology)
Quantitative HBV-DNA
Resistance and HBV Genotype
Hepatitis C Ac.
 Quantitative HCV-RNA Anti Hepatitis C Virus HCV
Genotyping
Detection of HCV RAVs (NS3)
Detection of HCV RAVs (NS5A)
Epstein Barr Virus (EBV) Mononucleosis Latex Test or Monotest
Ac. anti-VCA (IgG) EBV
Ac. anti-VCA (IgM) EBV
Ac. antinuclear antigen EBV (anti-EBNA)
Ab anti-Early Antigen Epstein Barr Virus (anti-EA)
qualitative EBV-DNA (PCR)
quantitative EBV-DNA (quantitative PCR)
Cytomegalovirus (CMV) Qualitative CMV-DNA (CMV PCR)
Quantitative CMV-DNA (CMV Q PCR)
CMV genotype
Ac. anti-Cytomegalovirus (IgM) Ab
. anti-cytomegalovirus (IgG)
Rashes Measles. Specific IgM and IgG antibodies.
Rubella. Specific IgM and IgG antibodies.
Pharyngeal discharge (scarlet fever)
Antistreptolysin "O" (ASTO)
Syphilis VDRL
FTA (Indirect Immunofluorescence)
TPHA (Microhemagglutination)
Toxoplasmosis Indirect Immunofluorescence (IFI)
Hemagglutination
Electrochemiluminescence / ELISA (IgM, IgG)
Avidity Test (IgG)
Polymerase Chain Reaction (PCR)
Chagas disease Indirect Immunofluorescence (IFI)
Hemagglutination
Electrochemiluminescence / ELISA (IgG)
Polymerase Chain Reaction (PCR)
Spermatic fluid Spermogram
Prostatic acid phosphatase
Fructose
Citrate
Zinc
Neutral alpha-glucosidase
Cerebrospinal fluid Physical-chemical
Direct examination and culture
Proteinogram and oligoclonal bands
Immunological studies Level 1 Proteinograma
IgG-IgA-IgM-IgE
Acs anti Streptococcus
Toxoide
Level 2 CD3-CD4-CD8-CD19-CD56 (LB, LT, NK)
TTB PHA
Oxidative metabolism Neutrophils
IgG subclasses
Level 3 Molecular studies of primary immunodeficiencies
Complement system studies Complement total activity (CH50)
Complement C3
Complement C4
Complement C1Q
Complement C1 INHIBITOR ESTERASE
Allergies Specific Immunoglobulin E (RAST IGE)
Total IgE
IgG4
Tryptase
Urine
Histamine Blood Histamine Histamine
Release Test (TLH)
Basophil Activation Test (TAB)
Lymphocyte Transformation Test (TTL)
Autoimmune diseases Rheumatoid arthritis AC. anti-citrulline cyclic peptite (anti-CCP)
FR
Rosse Ragan
PCC
PCR
Erythosedimentation
FAN
Ac. anti-ENA
Synovial fluid analysis
Lupus erythematosus Ac. anti-Sm
Ac. anti-DNA
Ac. anti-Ro
Ac. anti-La
Ac. Anti-native DNA (Critidia)
Antinuclear Factor (AN) Ab
anti lupus
Lupus anticoagulant
Ab. anti-cardiolipins (IgA, IgG, IgM) Ab
. Total antiphospholipids (IgM and IgG)
Ac. anti-beta2-glycoprotein (IgM and IgG)
Sjogren's syndrome Ac. anti-Ro
Ac. anti-La
FAN
FR
Scleroderma anti- AScl- 70 (diffuse ES)
Centromere (limited ES, CREST)
Rna-polymerase III (diffuse ES)
Fibrilarin 
Antiphospholipid syndrome AC. anti-total phospholipids (IgM
AC. anti-total phospholipids (IgG)
AC. anti-Cardiolipin (IgG)
AC. anti-Cardiolipin (IgM)
AC. anti-Cardiolipin (IgA)
AC.-anti-phosphatidyl serine (IgG)
Anticoagulant lupus
AC. anti-B2 Glycoprotein (IgG)
AC. anti-B2 Glycoprotein (IgM) 
Rheumatic fever ASO
Vasculitis Needle. Anti-Proteinase 3 (ANCA-C)
Ac. Anti-Myeloperoxidase (ANCA-P) 
Ankylosing spondylitis HLA-B27 ANTIGENO 
Myeloma Proteinogram
Immunofixation
quantitation of K / L Total IgG and IgA freely-IgM
Dermatomiositis anti-Jo-1 (histidyl)
anti-PL-7 (threonyl)
anti-PL-12 (alanyl)
anti-EJ (glycyl)
anti-OJ (isoleucyl)
anti-KS (asparaginyl)
Neuroinmunología Ac anti - HU
Ac anti - YO
Ac anti - RI
Ac anti - ANFIFISINA
Ac anti - MA
Ac anti - CV2
Ac anti - RECOVERINA
PANEL AC.NEURONALES: Anti-anfifisina, Anti-CV2, Anti-PNMA2 (Ma2 / Ta), Anti-RI, Anti-YO, Anti-HU, Anti-recoverina, Anti-SOX1, Anti-Titina, Anti-Zic4, Anti-TR (DNER)
Ac anti-N-METIL-D-ASPARTATO (NMDA) IGG
Ac anti -N-METIL-D-ASPARTATO (NMDA) IGG en LCR
PANEL AC ENCEFALITIS AUTOINMUNE: Anti-NMDAR, Anti-AMPAR1, Anti-AMPAR2, Anti-CASPR2, Anti-LGI1, Anti-GABA-R
Ac anti-MNO / AQP4
Ac anti-GANGLIOSIDOS PANEL
Ac anti-GM1
Ac anti-MAG-SGPG
Ac anti-RECEPTOR ACETILCOLINA (
ACRA ) MUSK
BANDAS OLIGOCLONALES (isoelectroenfoque)
OLIGOCLONAL BANDS (electrophoresis)
IgG INDEX in CSF
BASIC MYELIN PROTEIN
Hormonal determinations: studies of the endocrine axes Female sex hormones LH
FSH
Estradiol 
Progesterone
Prolactin
Total / free
testosterone Bioavailable testosterone
Male sex hormones  
Total / free testosterone
LH - FSH - prolactin
Spermogram-sperm culture
Gonadal axis LH-RH
test LH-RH intravenous infusion
test Testicular desensitization
test HCG test with repeated stimulation
Testobiron
test Clomiphene citrate test
Thyroid Thyroxine (T4)
Triiodothyronine (T3)
Thyrotrophin (TSH)
Free thyroxine (free T4)
ATG
ATPO
Extended
Thyroglobulin
Ac to Ultrasensitive Thyroglobulin
TRH test dosing TSH (See TRH test dosing TSH)
TBG
Anti-TSH receptor antibodies
T3 free
Prolactin axis Prolactin
Post HRT
Prolactin Test Post L-Dopa Prolactin Test Prolactin
Circadian Rhythm
Somatotrophic axis STH
IFG-1
IGF BP3
Exercise test dosing STH Exercise
test propanolol dosing STH
Clonidine test dosing STH
Insulin hypoglycemia
test dosing STH L-DOPA
test dosing STH TRH
test dosing STH Glucagon
test dosing STH Oral overload test a glucose dosing STH
GH-RH
test dosing STH LH-RH
test dosing STH Bromoergocriptine test dosing STH
Hypothalamic-pituitary-adrenal axis Cortisol 8 and 18 hours
Urinary free cortisol (urine 24 hours)
ACTH stimulus test (rapid test)
ACTH stimulus test (slow test)
Low-dose dexamethasone suppression test (NUGENT TEST)
High-dose dexamethasone suppression test (FORSHAM TEST)
Standard test with 2 mg dexamethasone (LIDDLE CHICO)
Standard test with 8 mg dexamethasone (LIDDLE BIG)
Adrenal 17 OH progesterone
17 OH progesterone post ACTH
DHEA
DHEA-Sulfate
Delta 4 androstenedione
Total / free / bioavailable testosterone
Cortisol
Adrenal medulla Norepinephrine-Dopamine Epinephrine-urine
adrenaline-noradrenaline-dopamine plasma
suppression test with clonidine
Posterior pituitary Water restriction
test ADH or agonist test (DDAVP)
Water overload test dosing ADH
Screening neonatal TSH
Galactosemia
Immunoreactive Trypsin
17-OH-Progesterone
Biotinidase
Phenylalanine

Extended Screening

Note: this list is intended to serve as a guide to the main laboratory tests that can be requested grouped according to the main profiles or clinical situations that the doctor wishes to investigate.

Links to consult laboratory test catalogs on the Mayo Clinic Reference Laboratory website:

To download Laboratory Test Catalog or Laboratory Test Interpretation Manual:
https://www.mayocliniclabs.com/test-catalog/print-catalog.html/index.html

For online search of laboratory tests:
https://www.mayocliniclabs.com/testcatalog/index.html

Laboratory tests by medical specialties:
https://www.mayocliniclabs.com/test-info/index.html

LabTests Online: Web in Spanish version fruit of the collaboration between Lab Tests Online in the USA (AACC), the European Association of Manufacturers of Diagnostic Material (EDMA), the Spanish Society of Clinical Biochemistry and Molecular Pathology (SEQC) and FENIN (Federation Spanish of Health Technology Companies).
https://labtestsonline.es/

List of new (emerging) technologies applied to clinical diagnosis.

Bibliography:

  • Fundamentals of Clinical Interpretation of Laboratory Tests, Guillermo Ruiz Reyes / Alejandro Ruiz Argüelles, 3rd edition, 2017. Editorial Médica Panamericana.
  • Laboratory Medicine: Fundamentals and applications in clinical diagnosis. Italo Antonozzi, Elio Gulletta, 2015. Editorial Médica Panamericana.
  • Errors in the clinical laboratory, Ruth Cano Corres, Clinical Laboratory, Bellvitge University Hospital, L'Hospitalet de Llobregat, Xavier Fuentes Arderiu, Clinical Laboratory Science Consultant, Barcelona
  • Interpreting laboratory results: change reference value and delta-check. Dr. Gabriela D´Isa1, Marta Rubinstein Medicina Infantil 2012; XIX: 8 - 13
  • Importance of biological variability and medical relevance, Mexican Journal of Clinical Pathology, Volume 50, Number 3, July - September 2003. Biological variation. Review from a practical perspective, Carmen Ricós, Carmen Perich, Marivı´ Doménech, Pilar Fernández, Carmen Biosca, Joana Minchinela, Margarita Simón, Fernando Cava, Virtudes Álvarez, Carlos Victor Jiménez and José Vicente García Lario, Magazine of the C línico laboratory. 2010 ; 3 (4): 192-200.
  • Managing and Validating Laboratory information Systems; Approved Guidelines, Vol 26, Nro. 36. Clinical and laboratory Standards Institute, December 2006.