Addressees and Objectives
Addressees and Objectives
This guideline is directed at all people with type 1 diabetes and all occupational
groups that care for people with type 1 diabetes, especially:
-
Registered diabetologists,
-
General practitioners and internists,
-
Doctors working in hospitals (diabetes specialists, anaesthesiologists,
surgeons, radiologists),
-
Nurses/professional caregivers (in the operating theatre
and/or wards or in the field of diagnostics) and
-
Outpatient or inpatient diabetes consultants and other professional groups in
diabetology.
In addition, the guideline is directed at higher-level institutions such as health
insurance companies or medical services.
In preparing and updating these guidelines, the authors pursue the following
objectives:
-
Reduce the rate of diabetes-associated complications and diabetes-associated
secondary damage. The diagnosis and treatment of lipodystrophy is also
described for the first time;
-
Improve the quality of life of people with type 1 diabetes;
-
Contribute to the adequate care of people with type 1 diabetes in hospitals,
both in regular and intensive care units. In particular, the implementation
of safe protocols to protect against hypoglycaemia in intravenous insulin
therapy should be supported;
-
Ensure correct treatment of acute complications and thus reduce the risk of
complications due to treatment;
-
Reinforce the correct training of people with type 1 diabetes, especially in
the outpatient sector.
Definition and Classification of Type 1 Diabetes
Definition and Classification of Type 1 Diabetes
Currently, the disease diabetes mellitus is classified into 4 main types (as per
etiological classification) according to the American Diabetes Association ADA [1]:
-
Type 1 diabetes (as a result of autoimmune beta-cell destruction, which
usually leads to absolute insulin deficiency), Subform: idiopathic;
-
Type 2 diabetes (due to progressive loss of insulin secretion from the beta
cell, often against the background of insulin resistance);
-
Other specific diabetes types (subtypes A: genetic defects of beta cell
function; B: genetic defects of insulin efficacy; C: exocrine pancreatic
disease, D: diabetes due to endocrinopathies; E: drug or chemical-induced;
F: diabetes resulting from infections; G: rare forms of immune-mediated
diabetes; H: other genetic syndromes occasionally associated with
diabetes);
-
Gestational diabetes (glucose tolerance disorder diagnosed for the first time
in pregnancy with a 75 g oral glucose tolerance test).
Type 1 diabetes occurs primarily in younger years but can also manifest itself in
later life. Even today, when type 1 diabetes is diagnosed, a severe metabolic
derailment in the form of ketoacidosis can be seen in about 15–30%
of cases, reaching as far as loss of consciousness [2].
Within the category type 1 diabetes, 2 subtypes are currently distinguished: the
immune-mediated form and the idiopathic form.
Type 1 diabetes (immune-mediated, autoimmune disease)
Type 1 diabetes (immune-mediated, autoimmune disease)
Type 1 diabetes is caused by a cell-mediated, chronic autoimmune destruction of beta
cells. The following serological markers are suitable for diagnosing type 1 diabetes
[3]
[4]
[5]
[6]
[7]
[8]:
-
Islet cell antibodies (ICA)
-
Insulin autoantibodies (IAA) (for children and adolescents but not for
adults)
-
Autoantibodies against glutamate decarboxylase of the B cell (GAD65A)
-
Autoantibodies to tyrosine phosphatase (IA-2ª) and IA-2ß
-
Autoantibodies against the zinc transporter 8 of the B-cell (ZnT8)
Type 1 diabetes is diagnosed when one or more of these autoantibodies are detected.
At least one of these autoantibodies is detectable in 85–90% of
patients with stage 3 diagnosis, i. e. simultaneous hyperglycaemia.
Idiopathic type 1 diabetes
Patients with idiopathic type 1 diabetes have a permanent insulin deficiency, tend
to
repeated episodes of ketoacidosis and are autoantibody negative, without
etiopathogenetic classification of autoimmune type 1 diabetes. There is no
association with HLA risk alleles. This form of type 1 diabetes is inherited with
high penetrance, occurs very rarely and is predominantly in patients with an Asian
or African background [9]. 1
Therapy Goals
The therapy for type 1 diabetes aims to avoid diabetes-related reductions to the
quality of life. It is also important to achieve for those affected to accept the
disease and be satisfied with the therapy regime.
In order to avoid diabetes-related reductions to the quality of life, the therapy
should be designed in such a way that the risk of severe metabolic disorders (severe
hypoglycaemia and/or severe hyperglycaemia with ketoacidosis or diabetic
coma) is as low as possible. Furthermore, the therapy should be conducted in such
a
way as to reduce the risk of developing microangiopathies (retinopathy, nephropathy)
and other diabetes-associated secondary damage (neuropathy, accelerated
macroangiopathy).
A further therapeutic goal in the treatment of type 1 diabetes is to avoid additional
risk factors for consequential damage. This is done by monitoring and, if present,
undergoing proper therapy for blood pressure, lipid profile and obesity-induced
insulin resistance. The documentation in the Diabetes Health Pass (Gesundheitspass)
can be helpful.
|
Recommendations
|
Degree of recommendation
|
|
In adults with type 1 diabetes, an HbA1c value of
7.5% (≤ 58 mmol/mol) should
be targeted at ≤ as long as no problematic
hypoglycaemia occurs. [10]
[11]
|
B
|
|
In adults with type 1 diabetes, HbA1c
≤ 6.5% (≤
48 mmol/mol) may also be targeted if there
is a low intrinsic risk of hypoglycaemia (e. g. new
onset of type 1 diabetes, stable low glycaemic viability).
[10]
[11] (strong consensus)
|
0
|
|
In adults with type 1 diabetes, a less tight HbA1c value
< 8.5% (69 mmol/ mol) should
be sought if therapy safety cannot be guaranteed, if severe
hypoglycaemia has frequently occurred, extensive
comorbidities or advanced macrovascular complications are
present. [10]
[11] (strong consensus)
|
B
|
|
Adults with type 1 diabetes with an HbA1c value >
9% (75 mmol/mol) or higher can be
assumed to have polyuria symptoms and a significantly
increased risk of secondary diseases. Expert consensus
(strong consensus)
|
Statement
|
|
In people with type 1 diabetes and severe hypoglycaemia in
recent months, the HbA1c target should be raised. [12]
[3]
[4]
[5]
[6]
[7]
[8]
[9]
[10]
[11]
[12]
[13]
[14] (strong consensus)
|
B
|
|
In people with type 1 diabetes and low life expectancy or
significant comorbidities, an increase in blood glucose can
be considered with the sole therapeutic goal of symptom-free
treatment. [15] (strong
consensus)
|
0
|
Therapy for Type 1 Diabetes
Therapy for Type 1 Diabetes
The type 1 diabetes therapy concept consists of insulin therapy, nutritional
knowledge, training, glucose self-monitoring and psychosocial care.
Insulin therapy
The indication for insulin therapy in type 1 diabetes is permanent and lifelong.
A prerequisite for the substitution of lacking insulin in people with type 1
diabetes is knowledge of the physiological insulin requirement as well as the
pharmacokinetic and pharmacodynamic properties of the insulins used for therapy
([Table 1]). For the planning of insulin therapy,
the following are also important: (a) consideration of how the additive insulin
requirement depends on the dietary intake (prandial insulin always in addition
to basal insulin requirement) and (b) the ratio between basal and prandial
insulin requirement.
Table 1 Types of insulin - efficacy, adverse effects, interactions and contraindications
(with data from [16]).
|
Effect
|
|
Onset
|
Maximum
|
Duration
|
Usually used
|
References
|
|
Human insulins
|
|
NPH insulin
|
1–2 h
|
6–7 h
|
14 h
|
2×daily
|
[17]
[18]
|
|
Normal insulin
|
30–60 min
|
3 h
|
8 h
|
0–30 min before meals
|
[19]
|
|
Mixed insulin NPH (70)/Normal (30)
|
30–60 min
|
3–3.5 h
|
14 h
|
Before breakfast and dinner
|
[20]
[21]
|
|
Insulin analogues
|
|
Degludec
|
1–2 h1
|
8–14 h low
|
> 42 h
|
1× daily
|
[22]
[23]
[24]
|
|
|
maximum
|
|
|
|
|
Detemir
|
1 h
|
7–9h
|
19–26 h
|
1 or 2 × daily
|
[18]
[25]
[26]
|
|
Glargin U100
|
1 h
|
8–12 h
|
20–27 h
|
1 or 2 × daily
|
[25]
[26]
[27]
|
|
Glargin U300
|
1–6 h1
|
12–16 h low
|
30–32 h
|
1 × daily
|
[27]
[28]
|
|
|
maximum
|
|
|
|
|
Aspart
|
20–25 min
|
120–150 min
|
4–5 h
|
0–15 min before meals
|
[29]
[30]
|
|
Alulisin
|
20–25 min
|
120–150 min
|
4–5 h
|
0–15 min before meals
|
[19]
|
|
Lispro
|
20–25 min
|
120–150 min
|
4–5 h
|
0–15 min before meals
|
[31]
|
|
Faster Aspart
|
15 min
|
120 min
|
4 h
|
Immediately before meals
|
[29]
|
|
Mixed insulin protamine. Aspart
|
20–25 min
|
2–3 h
|
10–14 h
|
0–15 min before breakfast and dinner
|
[30]
[31]
[32]
[33]
|
|
(70)/Aspart (30);
|
|
|
|
|
|
|
protamine. Lispro (70), Lispro (30)
|
|
|
|
|
|
|
Combination insulin
|
20–25 min
|
2–3 h
|
> 30 h
|
0–15 min before one or before two main
meals
|
[34]
[35]
|
|
Degludec (70)/Aspart (30)
|
|
|
|
|
|
1 Under steady state conditions, the time of onset of action
is of low clinical relevance due to the long effect and the flat action
profile.
Individual insulin needs
In principle, the individual insulin requirement of people with type 1 diabetes
resulting from an absolute insulin deficiency depends on the physiological
insulin secretion. This occurs both without food intake (=basal insulin
requirement) and after food intake (=prandial insulin requirement),
i. e. discontinuous and pulsatile. When dosing insulin, it must be taken
into account that the absolute insulin requirement also depends on the
individual insulin sensitivity of the respective patient. The therapeutic
insulin requirement can therefore only be deduced preliminarily based on the
insulin secretion of a healthy person.
Strategies of insulin therapy
Simple and more complex (intensified) strategies are available for insulin
therapy.
Conventional therapy
Conventional therapy is characterized by a binding specification of both the
insulin dose and the sequence and size of the meals (fixed carbohydrate
portions). A blood glucose self-measurement is recommended 3–4 times
daily. As a rule, fixed insulin mixtures are used, which are administered twice
a day for breakfast and dinner and, as far as possible, adapted to the eating
behaviour of the patients. A simple conventional insulin therapy can only be
successful with a fixed diet plan.
In contrast to intensified therapy, this form of insulin therapy is a subordinate
therapy option for people with type 1 diabetes in the following cases:
-
For people who cannot meet the requirements of an intensified therapy
(due to cognitive impairment, illness or age),
-
For people who decide against intensified therapy after receiving
extensive information on the risks and benefits,
-
For people with a significant problem adhering to long-term
therapies.
Since medium and long-term glycaemic control is crucial for reducing the risk of
diabetes-associated complications, conventional insulin therapy can be
sufficient if the individual HbA1c target values are reached, hypoglycaemia is
avoided, and the quality of life is not restricted by the therapy.
|
Recommendations
|
Degree of recommendation
|
|
Self-management using rtCGM or iscCGM (FGM) should be offered
if individual therapy goals are not achieved. Expert
consensus (strong consensus)
|
B
|
|
In order to use the advantages of a rtCGM/iscCGM
system effectively, adequate training and regular diabetic
care by diabetic teams experienced in the use of these
systems are required. Expert consensus (strong
consensus)
|
statement
|
|
Recommendations
|
Degree of recommendation
|
|
For people with type 1 diabetes, neither a specific form of
nutrition or diet is required, nor are specific diet foods
required. They are subject to the general recommendations on
healthy eating. Expert consensus (strong consensus)
|
Statement
|
|
Recommendations
|
Degree of recommendation
|
|
The disease type 1 diabetes should be clearly indicated in
the medical record during a hospital stay. Expert consensus
per [65] (strong consensus)
|
A
|
|
In all people with type 1 diabetes, an order to monitor blood
glucose must be issued during an inpatient stay. Trained
patients should be able to continue self-management as far
as possible. The blood glucose levels should be accessible
to all treating members of the healthcare team. If no HbA1c
value from the last 3 months is available, this should be
determined. Expert consensus (strong consensus)
|
A
|
|
Hospitalized patients with type 1 diabetes should receive
intensified insulin therapy with basal insulin and bolus
insulin/pump therapy. Expert consensus per [11] (strong consensus)
|
A
|
|
Recommendations
|
Degree of recommendation
|
|
The administration of fast-acting insulin only for correction
by means of a post injection plan is inferior to such
insulin therapy; for this reason, the administration of
insulin should not exclusively take place in the form of a
post injection plan. Expert consensus per [11] (strong consensus)
|
B
|
|
Recommendations
|
Degree of recommendation
|
|
People with type 1 diabetes and clinical suspicion of
moderate or severe diabetic ketoacidosis should be admitted
to hospital immediately. They should be treated in the
clinic on the basis of a detailed written treatment plan.
[75] (strong consensus)
|
A
|
|
The monitoring of people with type 1 diabetes who are being
treated for diabetic ketoacidosis should be carried out
under intensive medical conditions. During the treatment of
severe ketoacidosis, clinical evaluation and monitoring
should be performed at least every hour. Expert consensus as
per [67] (strong consensus)
|
A
|
|
Diabetic ketoacidosis should be treated according to the
following therapy principles:
|
A
|
-
Circulation stabilization with initial volume of 1 l
of isotonic solution (0.9% NaCl) in the
first hour; Then, additional liquids and
electrolytes equal depending on age, height, weight
and possible concomitant diseases (total fluid
intake can be up to 6 l/24 h and more for a
patient weighing 70 kg);
-
Potassium replacement already in the standard range
depending on the severity of the ketoacidosis by
administering 40 mEq/L potassium chloride
per 1000 ml NaCl 0.9%, example see
below;
-
Slow normalization of blood glucose using low-dose
insulin; intravenous insulin administration via
Perfusor (0.05–0.1 U/kg kg/h
IV).
-
Compensation of acidosis and ketosis (addition of
bicarbonate only at pH < 7.0 and then up to
a correction of 7.1);
-
Avoidance of therapy complications (hypokalaemia,
cerebral oedema);
-
Diagnosis and therapy of the triggering causes of
DKA. Expert consensus as per [76] (strong consensus)
|
|
Recommendations
|
Degree of recommendation
|
|
For diagnosing lipohypertrophy, an inspection of the
injection sites and palpation of the skin should be carried
out at least once a year, and quarterly in the case of
abnormalities and in particular in the case of inexplicably
fluctuating metabolic conditions. Expert consensus (strong
consensus)
|
B
|
|
From the age of 11 or after a diabetic duration of 5 years,
people with type 1 diabetes without known
diabetes-associated secondary diseases or comorbidities
should undergo the following early detection examinations on
a regular basis:
|
B
|
-
Determination of the albumin-creatinine ratio and
calculation of the glomerular filtration rate for
early detection of microalbuminuria and nephropathy.
Expert consensus EK IV as per [77] (strong consensus)
-
An ophthalmological retinal screening of fundus in
mydriasis
-
If no diabetic retinal changes are detected, the
screening interval should be two years for known low
risk (=no ophthalmological risk and no
general risk).
-
If the ophthalmologist does not know the general risk
factors, he should treat the patient as if the
patient had an unfavourable general risk profile;
for all other risk constellations, the screening
interval should be one year. [78] (strong consensus)
-
Anamnesis and examination for early diagnosis of
neuropathy, at least annually. Expert consensus as
per NVL neuropathy [79]
(strong consensus) Anamnesis and examination for
early detection of foot complications, at least
annually. Expert consensus as per [80] (strong consensus)
Examination of the cardiovascular system,
risk-adapted [Expert consensus as per [81].] In addition to a
physical examination, this includes the
determination of biochemical parameters for
cardiovascular risk factors, such as blood pressure
measurement, determination of blood lipids for the
early detection of lipid metabolism disorders.
Expert consensus (strong consensus)
|
Intensified therapy
The intensified insulin therapy is defined as the administration of at least
three insulin injections per day. Above all, however, it is characterised by
substituting the basal insulin requirement with long-acting basal insulin and by
substituting prandial insulin requirement with rapid-acting bolus insulin at
mealtimes (basal bolus principle). Synonyms of intensified insulin therapy are
functional insulin therapy and flexible insulin therapy. This therapy can be
performed with insulin syringes, insulin pens or insulin pump pens (see
recommendations).
Insulin types
There are currently two different groups of insulin available in Germany for
insulin replacement therapy for people with type 1 diabetes: human insulin and
insulin analogues ([Table 1]).
The use of animal insulin can be very necessary for a few people; the possibility
of importing animal insulin is hereby referred to.
|
Recommendations
|
Degree of recommendation
|
|
Human insulins (normal insulin or human insulins with delayed
onset of action) or insulin analogues (short-acting or
long-acting) are to be used for the therapy of people with
type 1 diabetes.[36]
[37]
[38]
[39]
[40]
[41]
[42]
[43] (strong consensus)
|
A
|
|
If strict therapeutic goals are pursued, the use of
short-acting and long-acting insulin analogues is associated
with advantages in terms of reducing HbA1c and risk of
hypoglycaemia as compared to normal insulin. [43]
[44]
[45] (strong
consensus)
|
Statement
|
Insulin application
Adequate handling and correct application of the insulin used are prerequisites
for successful insulin therapy. Information and review must be an integral part
of the structured training.
Continuous subcutaneous insulin infusion (CSII)
|
Recommendations
|
Degree of recommendation
|
|
In people with type 1 diabetes, the use of insulin pump
therapy should be examined if the individual therapy goals
are not achieved using intensified insulin therapy. [46]
[47]
[48]
[49]
[50]
(strong consensus)
|
B
|
|
In people with type 1 diabetes, the use of insulin pump
therapy should be checked in cases of frequent hypoglycaemia
or recurrence of severe hypoglycaemia using intensive
insulin therapy. [49]
[51] (strong consensus)
|
B
|
|
People with type 1 diabetes can be offered insulin pump
therapy in the following constellations:
|
In cases of frequently irregular daily routines, e.g. shift
work, activities with varying physical activity, problems
with the implementation of classic ICT/syringe
therapy (among other things to improve the quality of life)
[52, 53],
|
0
|
|
Recommendations
|
Degree of recommendation
|
-
In cases of planned pregnancy (begin before
conception) or at the beginning of a pregnancy,
-
For low insulin requirements, expert consensus
(EC/EK) IV,
-
In cases of insufficient glycaemic control of the
metabolic situation using ICT, e. g. dawn
phenomenon. [54]
[55]
[56]
[57]
[58] (strong consensus)
|
|
|
Prerequisites for the start of insulin pump therapy in people
with type 1 diabetes are:
|
-
Mastery of an intensified insulin therapy on the part
of the patient,
-
The provision of care by a qualified diabetology
staff with appropriate experience in the use of
insulin pumps,
-
Insulin pump therapy training by a well-trained
training team. Expert consensus (strong
consensus)
|
Statement
|
Blood glucose self-monitoring, rtCGM and iscCGM (FGM)
The precision of the blood glucose self-monitoring is sufficient for
self-management, even if it is lower compared to laboratory measurements [59]
[60].
Nutrition
It is of crucial importance for the therapy of type 1 diabetes that patients are
able to assess the glucose efficacy of their diet in order to adjust the insulin
dosage accordingly. Recommendations on the objectives, content and modalities of
training for type 1 diabetes are given in section 4.4
Training/structured training and treatment programmes.
Training/structured training and treatment programmes
In the treatment of type 1 diabetes, patients must – of their own accord
– implement the essential therapeutic measures (insulin substitution
usually several times a day, hypoglycaemia prophylaxis, etc.) in accordance with
their individual therapy goals. The success of therapy and the prognosis of
people with type 1 diabetes therefore depend very much on their ability to treat
themselves [61]
[62]
[63]. The knowledge and skills required for this are
taught in structured patient training courses. The training measures are
intended to enable patients (empowerment or capacity to self-manage)
“... to integrate diabetes into their own lives as best as possible on
the basis of their own decisions, to avoid acute or long-term negative
consequences of diabetes and to maintain their quality of life” [62].
Forms of diabetes training
Basic training
In basic training and treatment programmes, which should be carried out as
soon as possible after the manifestation of diabetes or the changeover to a
different therapy regime, basic knowledge and skills for the implementation
of diabetes therapy, for informed decision-making and for coping with the
disease are developed together with the patient. Repeated or supplementary
training measures have the primary objective of supporting patients with
type 1 diabetes in the event of difficulties in implementing therapy in
everyday life and of offering concrete assistance with problems related to
diabetes (e. g. lack of skills, problems in everyday life).
Problem-specific training and treatment programmes
These are aimed at patients in special, diabetic-specific problem situations
(e. g. occurrence of secondary diseases, problems with
hypoglycaemia). The indication for a problem-specific training and treatment
programme may be given if the patient has to implement a specific, new form
of therapy in everyday life (e. g. insulin pump therapy, continuous
glucose monitoring), if significant problems are associated with acute
complications (e. g. hypoglycaemia perception disorder) or in
connection with subsequent complications (e. g. neuropathy, sexual
disorders, diabetic foot, nephropathy, retinopathy, cardiovascular events)
or when special situations exist in everyday life which make the
implementation of the therapy more difficult (e. g. shift work,
fasting, psychological problems) [61]
[64].
Therapy in Special Situations
Therapy in Special Situations
Hospital stays
Therapy during travel
People with type 1 diabetes are not subject to significant restrictions on
travel activity and destinations solely because of having diabetes.
Restrictions, if any, result from secondary illnesses. It is often the case
that metabolic parameters deteriorate during a journey. Consultation before
travel and planning of the trip based on diabetes treatment are useful.
There are many well-made recommendations available for planning purposes by
self-help organisations, professional associations and also from government
organisations, mostly in the form of checklists. These checklists, at least
in the case of patients with type 2 diabetes requiring insulin, have also
been verified within studies [66] and have found
their way into most structured patient training courses.
Acute Complications
Diabetes-associated emergencies in people with type 1 diabetes are either the result
of insulin deficiency or insulin overdose. Both hypo- and hyperglycaemia can be
life-threatening ([Table 2]).
Table 2 Typical symptoms of hypoglycaemia (from [67]
[68]
[69]
[70]
[71]).
|
Autonomic symptoms
|
Neuroglycopenic Symptoms
|
General discomfort
|
|
Sweating Trembling Cravings Heart palpitations
|
Mental confusion Rapid, incoherent speech Difficulty in finding words Irritability Seeing double and other visual disorders Headaches Anxiety Sleepiness Difficulty with dexterity/coordination Limitation of awareness and action Unconsciousness Cramps
|
Nausea Headache
|
Hypoglycaemia
The prevention of hypoglycaemia is one of the greatest challenges in achieving a
blood glucose level as close as possible to the norm [11]
[67].
Definition/severities
The current international classification of hypoglycaemia into mild and severe
hypoglycaemia is not based on specific blood glucose values, but exclusively on
the ability for self-therapy [12]
[68]:
-
Mild hypoglycaemia: Hypoglycaemia can be independently treated with
carbohydrate intake by the patients.
-
Severe hypoglycaemia: The patient depends on outside help in treating the
hypoglycaemia (e. g. from relatives or medical personnel) ([Table 3]).
Table 3 Therapeutic measures in hypoglycaemic people with type
1 diabetes.
|
Mild hypoglycaemia
|
Severe hypoglycaemia
|
|
Therapy by patients possible
|
Patient is conscious, but therapy is no longer possible by
the patient.
|
If unconscious
|
|
Without IV access (e. g. by family/
others)
|
With IV access
|
|
20 g carbohydrates (preferably glucose; 200 ml fruit
juice also possible)
|
30 g carbohydrates (glucose)
|
1 mg glucagon IM or subq (Warning: Vomiting and
danger of aspiration)
|
50 ml 40% glucose1 in bolus IV
|
|
Measure blood glucose after 15 min and repeat therapy
if blood glucose concentration remains low
(50–60 mg/dl;
2.8–3.3 mmol/l). After successful
therapy, take a meal or snack to avoid recurring
hypoglycaemia.
|
If no response is received after 5 min of therapy at
the latest, repeat. After successful therapy, take a meal or
snack to prevent recurrent hypoglycaemia.
|
1 or 25 ml 40% glucose.
Causes and symptoms
In people with type 1 diabetes, hypoglycaemia is always the result of an absolute
or relative insulin overdose. Causes for insulin overdose can include [69]:
-
Insulin dosage is too high, insulin injection at the wrong time, or the
wrong type of insulin is injected
-
Decreased exogenous glucose intake (forgotten meals)
-
Glucose consumption is increased (e. g. after sports)
-
Endogenous glucose production is lowered (for example after alcohol
consumption, in case of renal insufficiency)
-
Insulin sensitivity is increased (during the night, after improved
glycaemic control, after improved physical fitness).
-
Insulin clearance is lowered (for example, in renal insufficiency).
Treatment of hypoglycaemia
People with type 1 diabetes and hypoglycaemia perception disorder can be offered
specific structured training (see section “Training/structured
training and treatment programmes”).
Diabetic ketoacidosis
Diabetic ketoacidosis (DKA) is a metabolic derailment due to an absolute or
relative insulin deficiency and consecutive metabolization of fatty acids, which
can occur with or without hyperosmolar diuresis and thus also without massive
hyperglycaemia. Causes of diabetic ketoacidosis:
Diabetic ketoacidosis occurs in clinical routine during:
-
Undetected first manifestation of type 1 diabetes mellitus,
-
Interruption of an ongoing insulin therapy,
-
Interruption of insulin administration during insulin pump therapy,
-
Acute, severe diseases associated with an increased, catabolic
metabolization and increased insulin requirements.
Biochemical definition and suspected diagnosis
Diabetic ketoacidosis is biochemically defined by:
-
Blood glucose > 250 mg/dl
(13.9 mmol/l)2 and
-
Ketonemia and/or
-
Ketonuria with arterial pH < 7.35 or
-
Venous pH < 7.3; serum bicarbonate <
270 mg/dl (15 mmol/l)
The suspected diagnosis of ketoacidosis must be made if persistent hyperglycaemia
> 250 mg/dl (13.9 mmol/l) is detected in
combination with ketonuria, in particular if this finding is accompanied by
corresponding clinical symptoms ([Table 4]) or a
comorbidity is present. Further laboratory tests are required to confirm the
diagnosis.
Table 4 Symptoms of diabetic ketoacidosis (from: [67]
[72]
[73]).
|
Gastrointestinal Symptoms
|
Loss of appetite, nausea and vomiting, abdominal pain up to
pseudo-peritonitis.
|
|
Symptoms of dehydration
|
Symptoms of dehydration are dry mouth, standing skin folds,
muscle cramps (calves, abdomen), soft bulbi, drop in blood
pressure, polyuria (primary), oliguria (secondary). The
cause is osmotic diuresis due to the increased blood glucose
concentration (up to 100–200 g
glucose/day!), which leads to a significant loss of
fluid. This can lead to microcirculatory disturbances and
hyperviscosity with thrombotic events.
|
|
Respiratory symptoms
|
The clinical characteristic of severe derailment is metabolic
acidosis, with respiratory compensation. To compensate an
acidosis with pH values of 7.1 and less, the carbon dioxide
partial pressure in the blood gas analysis drops down to 15
mmHg. The deep, laboured or slightly rapid breathing is
called Kussmaul’s respiration. The exhaled air
smells of acetone, the typical, fruity smell of
ketoacidosis.
|
|
Changes in consciousness
|
While the state of consciousness is not restricted in a mild
ketoacidosis, a ketoacidosis of moderate severity is
associated with restrictions of consciousness (drowsiness).
Patients with severe diabetic ketoacidosis are in a stupor
or comatose.
|
Symptoms
Laboratory chemical diagnostics
The following laboratory parameters are to be determined initially using
quality-controlled laboratory standards if diabetic ketoacidosis is
suspected: Blood glucose and ketones in urine or blood.
If these values are pathological, an arterial or venous blood gas test should
be carried out and potassium levels, serum creatinine, blood count and CRP
determined, as they have a decisive effect on the therapeutic regime. For
outpatients, an urgent transfer to hospital must be arranged. If infections
are suspected, bacterial cultures (e. g. blood, urine, pharynx)
should be created.
An extended diagnosis is to be carried out within the framework of causal
research and depending on the comorbid diseases.
([Table 6])
Table 6 Example of an infusion plan for the replacement of
liquid
|
Infusion solution
|
Quantity and period
|
|
0.9% NaCl 1000 ml with potassium
chloride
|
1000 ml over the next 2 h
|
|
0.9% NaCl 1000 ml with potassium
chloride
|
1000 ml over the next 2 h
|
|
0.9% NaCl 1000 ml with potassium
chloride
|
1000 ml over the next 4 h
|
|
0.9% NaCl 1000 ml with potassium
chloride
|
1000 ml over the next 4 h
|
|
0.9% NaCl 1000 ml with potassium
chloride
|
1000 ml over the next 6 h
|
|
Potassium levels in the first 24 h
(mmol/l)
|
Potassium administration per 1000 ml infusion
solution (mEq/l)
|
|
Higher than 5.5 3.5–5.5
< 3.5
|
no administration 40 Additional oral administration of
potassium, if necessary
|
After 12 h, the cardiovascular situation is to be assessed
and the liquid replacement adjusted accordingly.
Severity of diabetic ketoacidosis
The classification of diabetic ketoacidosis into 3 degrees of severity
follows the classification by the American Diabetes Association (ADA) [74] ([Table 5]).
Table 5 Degrees of severity of diabetic ketoacidosis.
|
Parameter
|
Degree of severity
|
|
Mild
|
Moderate
|
Severe
|
|
pH
|
< 7.3
|
≤ 7.2
|
≤ 7.1
|
|
Bicarbonate
|
< 270 mg/dl
(15 mmol/l)
|
≤ 180 mg/dl
(10 mmol/l)
|
< 90 mg/dl
(5 mmol/l)
|
People with type 1 diabetes significantly underestimate the danger of
ketoacidosis, as it is rather rare compared to the acute complication in the
form of hypoglycaemia. Often, training on the subject of ketoacidosis took
place a while ago and patients do not always remember how they can treat
ketoacidosis themselves. Therefore, at regular intervals during check-ups,
the topic should be addressed of recognizing ketoacidosis and treating it in
a timely manner. It would be recommended to develop an evaluated short
training module or other form of easily accessible information on
ketoacidosis (e. g. a smartphone app). Patients should always
remember that ketoacidosis is a dangerous medical situation and, in case of
doubt, immediate medical assistance should be sought through the emergency
medical services.
Control of diabetes-associated secondary diseases and associated risk
facto
Guideline Information
The evidence-based guideline was prepared on behalf of the German Diabetes
Society/Deutsche Diabetes Gesellschaft (DDG). President of the DDG
is Prof. Dr. med. Dirk Müller-Wieland (2017–2019).
Expert group appointed by the DDG Board
-
Prof. Dr. Thomas Haak, Bad Mergentheim (Coordinator)
-
Dr. Stefan Gölz, Esslingen
-
Prof. Dr. Andreas Fritsche, Tübingen
-
PD Dr. Martin Füchtenbusch, Munich
-
Dr. Thorsten Siegmund, Munich
Representatives of other organisations who voted on the recommendations
and commented on the content of the guideline:
-
Elisabeth Schnellbächer; Association of Diabetes Consultants
and
-
Training occupations in Germany/ Verband der
Diabetesberatungs- und Schulungsberufe Deutschlands, Birkenfeld
-
Prof. Dr. Horst H. Klein, German Society for Internal
Medicine/ Deutsche Gesellschaft für Innere Medizin,
Bochum
-
Dr. Til Uebel, German Society for General and Family
Medicine/ Deutsche Gesellschaft für Allgemein- und
Familienmedizin, Ittlingen
-
Diana Droßel, German Diabetes Aid - People with
Diabetes/ Deutsche Diabetes Hilfe – Menschen mit
Diabetes, Eschweiler
German Diabetes Association: Clinical Practice Guidelines
This is a translation of the DDG clinical practice guideline published in:
Diabetologie 2019; 14 (Suppl 2): S142–S152, DOI:
https://doi.org/10.1055/a-0898–7429