Nursing Nerds

GI, Hepatic, Hematology and Oncology Red Flags

Book 10 · Page 1010 / 15

Exhibit: the anemia that is being destroyed, not lost

Anemias grouped by mechanism: blood loss, decreased production, and increased destruction.
Fig 11.10 · pending clinical review

EXHIBIT — Tabs: Vital Signs · History and Physical · Laboratory Results · Provider Orders · Nurses' Notes

History and Physical 24-year-old with sickle cell disease. Third admission this year. Presents with severe bilateral leg and low back pain that began after a weekend outdoors in the cold with limited fluid intake. Reports the pain is like previous crises. Splenectomy at age 9.

Laboratory Results

Today 0530Prior visit
Hemoglobin7.4 g/dL7.6 g/dL
Hematocrit22 percent23 percent
Reticulocyte count12.4 percent9.8 percent
Lactate dehydrogenase648 units/L512 units/L
Total bilirubin3.4 mg/dL2.6 mg/dL
Indirect bilirubin2.9 mg/dL2.1 mg/dL
Haptoglobinless than 10 mg/dL14 mg/dL
White blood cells14,200/mm³9,800/mm³
Platelets402,000/mm³388,000/mm³
Peripheral smearsickled forms, target cells, Howell-Jolly bodiessickled forms

Vital Signs

060010001400
Temperature37.1 °C37.6 °C38.4 °C
Heart rate98108122
Blood pressure118/68112/64104/58
Respirations182228
Oxygen saturation97 percent, room air94 percent, room air89 percent, room air
Pain score9 of 108 of 108 of 10

Nurses' Notes — 1355 "Patient now reports discomfort across the chest, worse with a deep breath, with a dry cough that started this afternoon. Declined incentive spirometry twice this shift because of leg pain."

Provider Orders Isotonic intravenous fluid at a maintenance rate. Scheduled opioid analgesia around the clock with breakthrough dosing. Incentive spirometry every hour while awake. Oxygen titrated to saturation.

Anemia by mechanism

  • Loss. Acute bleeding is normocytic at first; chronic bleeding drains iron and trends toward small, pale cells.
  • Decreased production. Iron, vitamin B12, and folate deficiency, marrow failure, and the low erythropoietin of chronic kidney disease. Only B12 deficiency brings neurologic signs, and that is how it separates from folate deficiency.
  • Increased destruction. Sickle cell disease, autoimmune hemolysis, and transfusion reaction. Reticulocytes rise, lactate dehydrogenase and indirect bilirubin rise, and haptoglobin falls because it is consumed binding free hemoglobin.

Watch outfever, chest pain, and a falling oxygen saturation in sickle cell disease is acute chest syndrome, the leading cause of death in this population. It is escalated immediately, not managed as worsening pain.

Margin notenever ice a sickle crisis; cold causes the sickling.

Howell-Jolly bodies confirm functional asplenia, which is why any fever in this patient is treated as high risk. Meperidine is avoided for crisis pain because its metabolite accumulates and lowers the seizure threshold.

Takeawaya high reticulocyte count with high lactate dehydrogenase, high indirect bilirubin, and low haptoglobin means the cells are being destroyed, and in this patient the chest findings now outrank the pain.

Every value's reference range → BOOK 07 · P6. Pediatric splenic sequestration → BOOK 13 · P8. Opioid pharmacology → BOOK 05 · P6.