- Case Report
- Open Access
- Open Peer Review
Ketoacidosis in a non-diabetic woman who was fasting during lactation
© Hudak et al. 2015
- Received: 4 May 2015
- Accepted: 18 August 2015
- Published: 4 November 2015
Ketoacidosis is a potential complication of type 1 diabetes. Severe ketoacidosis with a blood pH below 7.0 is only rarely seen in other diseases.
Three weeks after delivery, a young woman was admitted because of tachypnoe and tachycardia. Blood gas analysis showed a severe metabolic acidosis with a high anion gap. Further workup revealed the presence of ketone bodies in the urine with normal blood glucose and no history of diabetes. The patient reported that she had not eaten for days because of abdominal pain. After initial treatment in the ICU and immediate re-feeding, the patient’s condition rapidly improved.
While under normal circumstances fasting causes at most only mild acidosis, it can be dangerous during lactation. Prolonged fasting in combination with different forms of stress puts breast feeding women at risk for starvation ketoacidosis and should therefore be avoided.
- Diabetic Ketoacidosis
- Normal Blood Glucose
- Prolonged Fasting
- Severe Metabolic Acidosis
- Relevant Family History
Severe acidosis is a potentially life-threatening condition. In case of metabolic acidosis, determination of the serum anion gap helps to narrow down the differential diagnosis. An increased anion gap indicates the presence of an unusual amount of an acid that is most commonly found in ketoacidosis, lactic acidosis, renal insufficiency, and intoxications while other causes are rare.
We report on a young woman who showed a severe metabolic acidosis with a high anion gap three weeks after delivery despite normal blood glucose and no history of diabetes. She was fasting while breast feeding due to constant abdominal pain.
Three weeks after delivery, a 32-year-old woman was admitted to our hospital because of tachypnoea and tachycardia. She was first presented to the gynaecological unit with constant abdominal pain since delivery. The birth had been experienced as traumatic by the patient, but reports documented no complications during the vaginal delivery. The newborn daughter was the first child of the patient and was healthy. There were no abortions in the past. The patient reported not to have eaten solid food for days because of nausea and vomiting, while fluid intake caused no problems. Micturation and defecation where normal, she had no fever. Her medical history included multiple deep vein thromboses in the past (seven, five, and two years ago). Therefore, she received prophylactic treatment with low molecular weight heparin during pregnancy and after delivery. A thrombophilia screening was not yet performed because the patient rejected it for personal reasons. There where no other relevant diseases in the past history and no relevant family history.
On admission, clinical examination revealed a muscular defense over the whole abdomen and tenderness in the lower left quadrant. Gynaecological physical examination was without pathological findings. Transvaginal ultrasound revealed an ovarian venous thrombosis on the left side which was confirmed by CT-scan. No additional locations of thrombosis were detected. The dose of low molecular weight heparin therapy was increased from a prophylactic to a therapeutic regiment.
Over the next hours, tachypnoea worsened while the oxygen saturation remained normal. Increasing tachypnoea, tachycardia and hyperventilation led to the referral of the patient to the internal medicine unit.
Admission to Internal Medicine
Day of admission - 6 h after initiation of treatment
7.35 – 7.45
75 – 100
33 – 45
21 – 26
Anion gap (mmol/l)
8 – 16
0.5 – 2.2
3.9 – 6.1
12.0 – 16.0
White-cell count (1/μl)
4100 – 11800
Platelet count (1000/μl)
150 – 450
136 – 148
3.5 – 4.8
2.1 – 2.6
0.8 – 1.5
Plasma creatinine (mg/dl)
0.5 – 0.8
Urine glucose, spot urine
Urine acetone, spot urine
Urine Phosphat (24-h urine collection, mmol/l)
Our patient was immediately transferred to ICU and an infusion of sodium bicarbonate (8.4 %), potassium-phosphate (50 mmol/50 ml), glucose (20 %), and saline was initiated via a central line. After these measures as well as after immediate re-feeding and discontinuation of breastfeeding, acid–base homeostasis started to normalize and tachypnoea subsided. After ten days, the patient had fully recovered and was discharged home.
Since we ruled out all other common forms of increased anion gap metabolic acidosis (Table 1) and because of the rapid response to re-feeding, we diagnosed starvation ketoacidosis in lactation. While under normal circumstances fasting causes at most only mild acidosis, it can be dangerous during lactation. The increased energy demand for milk production causes enhanced gluconeogenesis, decreased insulin secretion, lipolysis, and can subsequently induce ketogenesis . Some reports termed this condition “bovine ketosis” [4, 5] since it is also common in dairy cows that can sometimes not compensate for the high energy requirements of milk production by sufficient energy intake . In humans, this condition is rare; we are aware of only five cases in the literature [4, 5, 7–9]. Just as in our patient who suffered from abdominal pain, there was an additional stressor present in the other reported patients. Thus, prolonged fasting in combination with different forms of stress seems to put breast feeding women at risk for starvation ketoacidosis.
Given the potential harms of this life-threatening condition, complete fasting should be avoided during lactation. If fasting is necessary for medical reasons, sufficient glucose should be administered parenterally. If a patient develops starvation ketoacidosis, glucose should be administered immediately and the woman should stop breast feeding.
Written informed consent was obtained from the patient for publication of this Case Report.
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