transplant Flashcards

1
Q

post-chronic GVHD pulm illness

A

bronchiolitis obliterans- narrowing of airways, wheeze, CXR normal, CT shows thickening, bronchiectasis. PFT- obstructive, can be stabilized with increased immunosuppression.

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2
Q

parainfluenza

A

must delay, as pneumonia is fatal in 30%; wait until PCR negative

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3
Q

re-vaccination

A

12 months post-transplant, not altered by other factors such as immunosuppression

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4
Q

AVN of hip

A

common post-Allo comp: associated with steroids and TBI

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5
Q

chronic GVHD

A

usually requires re-institution of immunosuppressants, very long slow taper, but usually possible; sicca-like symptoms, rash, higher rates in peripheral blood aloo, calcineurin inhib/prednisone can treat 50-70%,

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6
Q

acute GVHD

A

rash, n/v/diarrhea, ileus, jaundice

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7
Q

immunosuppressants

A

if no GVHD can taper at 3 months, discontinue at 6 months

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8
Q

Palifermin

A

reduces duration of GVHD

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9
Q

SCT for thalassemia

A

best results if done before hepatomegaly or fibrosis. 70-90% cure

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10
Q

alloSCT results for AML/ALL

A

50-70% 5-yr DFS.

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11
Q

CML transplant

A

restrict to progression following TKIs

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12
Q

HLA class 1 determinents

A

HLA-A, HLA-B, HLA-C. class 2: HLA-DP, DQ, DR (ch 6). low recombination frequency

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13
Q

liklihood of finding a HLA matched sibling

A

1- .75^n (n is number of siblings). if n=2, then ~45%. ABO not expressed on stem cells, so doesn’t matter

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14
Q

mismatching and outcome

A

mismatch slightly worsens leukemia relapse outcomes.

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15
Q

tolerability of HLA mismatches

A

HLAB and HLA-C are better tolerated. HLA A and DRB1 less tolerated. if peripheral CD34+ used, then HLAC mismatch less tolerated

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16
Q

marrow transplantation

A

serial aspirations- 10mL. need 1-1.5L marrow

17
Q

Peripheral marrow collection

A

faster engraftment, CD34 selection and mobilization with G-CSF or GM-CSF. can use plerixafor (CXCR4 antagonist) to mobilize cells if G-CSF insufficient. (10-20% fail to mobilize with G alone)

18
Q

umbilical transplant

A

double reduces graft failure and enhances graft v tumor

19
Q

preparative regimen before transplant for nonmalignant conditions

A

aplastic anemia- needs ATG or CTX. SCID doesn’t need because immunocompromised

20
Q

DLI dosing

A

1 x 10^7–> remission of 70% with CML

21
Q

engraftment after allo

A

marrow: 1-2 weeks after, peripheral ALC increases. day 26- ANC 1000. plts recover with neutrophils. PMBC- one week sooner, umbilical- one week later.

22
Q

graft rejection

A

more common with weaker conditioning regimens, or if a lot of transfusions were given before trx, or more mismatched, or T-cell depleted. can try to tx with GMCSF, or repeat transplant with conditioning.

23
Q

acute GVHD

A

within 3 months- rash, GI, jaundice cholestasis. classic is 100d. Tx is combination MTX/MMF and calcineurin inhibitior (cyclosporine or tacro). Tx for 3 months from Trx then taper and d/c at 6 months.

24
Q

risk factors of acute GVHD

A

mismatching, old age pt or donor, multiparous donor, more intensive conditioning regimens

25
Q

chronic GVHD

A

like a collagen vascular disease. frequent in mismatched, in peripheral trx, and if prior acute GVHD. tx is steroids/calcineurin inhibitor. most pts can taper, but sometimes over months/years.

26
Q

prophylaxis for chronic GVHD tx

A

bactrim + penicillin- PCP and encapsulated organism.

27
Q

autoimmune conditions after alloSCT

A

5%. hemolytic anemia, ITP. tx with cyclosporine, pred, or ritux

28
Q

Trx infection prophy

A

anti-fungal: flucon or voricon

29
Q

HSV prophy after transplant, CMV prophy

A

IV acyclovier 250mg q8hr starteing 1 week before Trx and 1 month after Trx. can use gancyclovire st time of engraftment to reduce risk if latent CMV before. reduced risk of CMV with lymphodepleted blood products.

30
Q

gancyclovir toxicities

A

granulocytopenia. responds to G-CSF. foscarnet good salvage, but causes electrolyte wasting

31
Q

late post-trx infection

A

VZV (>3 months0. if chronic GVHD–>bacterial/fungal –> use propgy bactrim, penn, acyclovir.

32
Q

post-transplant vaccination

A

1 year after: tetanus, diphtheria, heme inf, polio, pneumococcal. MMR/VZV/Pertussus at 24 months.

33
Q

oral mucositis associated with preparative regimens

A

5-7 days post. need PCA pump. palifermin can shorten duration of mucositis

34
Q

SOS

A

1-4 weeks post prepchemo. 5%. possible treat with difibrotide. prophylax with ursodeoxycholic acid.

35
Q

idiopathic pneumonia syndrome

A

3-6 month post-trx related to chemo. 5% of pts. frequent following high-dose radiation. 50% mortality, no treatments.s

36
Q

PTLD following transplant

A

high-dose chemoradiotherapy at increased risk, T-cell depletd at risk,.

37
Q

DLI success by malignancy type

A

CR rate: CML 70%, advanced CML 12%, AML/MDS 29%, ALL 0%. half develop GVHD, 20% mortality. keep less than 10x10^7 cells.

38
Q

CML relapse after transplant, options

A

DLI, interferon (35% CR)