Page 915 - Saunders Comprehensive Review For NCLEX-RN
P. 915

considerably in severity and frequency; these include vaso-occlusive crisis, splenic
               sequestration, hyperhemolytic crisis, and aplastic crisis. Sickle cell crisis may be
               precipitated by infection, dehydration, hypoxia, trauma, or physical or emotional
               stress. The mother of a child with sickle cell disease should encourage fluid intake of
               1.5 to 2 times the daily requirement to prevent dehydration.
                  Test-Taking Strategy: Note the strategic words, need for further instruction. These
               words indicate a negative event query and ask you to select an option that is an
               incorrect statement. Recalling that fluids are a main component of treatment in sickle
               cell anemia to prevent crisis will direct you to the correct option. Remember that
               fluids are required to prevent dehydration.
                  Level of Cognitive Ability: Evaluating
                  Client Needs: Health Promotion and Maintenance
                  Integrated Process: Teaching and Learning
                  Content Area: Pediatrics: Hematological
                  Health Problem: Pediatric-Specific: Anemias
                  Priority Concepts: Client Education; Clotting
                  References: Hockenberry, Wilson, Rodgers (2017), pp. 791-792.


                   307. Answer: 3


                  Rationale: Hemophilia refers to a group of bleeding disorders resulting from a
               deficiency of specific coagulation proteins. The primary treatment is replacement of
               the missing clotting factor; additional medications, such as agents to relieve pain,
               may be prescribed depending on the source of bleeding from the disorder. A child
               with hemophilia A is at risk for joint bleeding after a fall. Factor VIII would be
               prescribed intravenously to replace the missing clotting factor and minimize the
               bleeding. Factor X and iron are not used to treat children with hemophilia A.
                  Test-Taking Strategy: Focus on the child’s diagnosis. Eliminate options 2 and 4
               because they are comparable or alike. Recalling that a child with hemophilia A is
               missing clotting factor VIII will direct you to the correct option from those
               remaining.
                  Level of Cognitive Ability: Analyzing
                  Client Needs: Physiological Integrity
                  Integrated Process: Nursing Process—Planning
                  Content Area: Pediatrics: Hematological
                  Health Problem: Pediatric-Specific: Bleeding Disorders
                  Priority Concepts: Clinical Judgment; Clotting
                  Reference: McKinney et al. (2018), pp. 1130, 1132.


                   308. Answer: 2

                  Rationale: In iron deficiency anemia, iron stores are depleted, resulting in a
               decreased supply of iron for the manufacture of hemoglobin in red blood cells. An
               oral iron supplement should be administered through a straw or medicine dropper
               placed at the back of the mouth, because the iron stains the teeth. The parents should
               be instructed to brush or wipe the child’s teeth or have the child brush the teeth after
               administration. Iron is administered between meals because absorption is decreased



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